Scientific Basis for
Ayurvedic Therapies
edited by
Brahmasree Lakshmi Chandra Mishra
An acute attack may lead
to delusions, loss of appetite, nasal
discharge, and thirst. With increasing intensity of bouts,
the patient may become unconscious. The
patient finds relief for a few moments after
expectoration of sputum, breathes with great
difficulty while lying down, and finds
comfort while sitting. The patient’s eyes are
wide open, and he or she perspires from the
forehead, suffers dryness of mouth, gets
bouts of dyspnea (often with shivering), and
desires additional warmth. The disease
greatly increases on cloudy days and in rain, cold,
or direct breeze and other factors that may
cause an increase of
kapha
. In addition there
is throat irritation, vomiting, and anorexia.
This description is quite similar to what we
understand today.
Tamaka svasa
has been classified into two varieties:
Tamaka svasa
vatapradhan
(
vata
dosa
is
predominant) and
Tamaka svasa shlesma pradhan
(
kapha
dosa
is predominant). The indicators
of the former are highly painful breathing
with high frequency of noisy sounds, little
expectoration, difficulty in expectoration,
and insomnia. The latter is characterized by high
vibrating noise in throat while breathing,
coryza, easy and copious expectoration, and
painful fast breathing.
The clinical manifestations of asthma as we
see it today include episodes of shortness
of breath, cough, wheezing, and chest
tightness. Patients with more severe cases are likely
to have persistent symptoms, worsening at
night and early mornings. Often the chest
congestion takes more than 10 days to clear
up. The symptoms may be precipitated by
exposure to the various stimuli discussed
above. Very often, exacerbations occur in the
absence of any well-defined exposure,
particularly in patients with persistent disease.
These symptoms usually respond to
bronchodilators; this response supports the diagnosis
of asthma.
The practitioners of Ayurveda confirm the
diagnosis by a detailed case history of the
patient and objective examination to
determine the imbalances between various constituents.
An evaluation is made about the patient’s
body constitution, state of digestion, and
level of activity through interrogation.
Interrogation also includes questions on precipitating
and pacifying factors and lifestyle. A
detailed physical examination of all systems,
including checking the pulse and tongue, is
done to identify the specific type of
dosa
involved in the pathology. Diagnosis is
finally made based on the symptoms, which are
dependent on the location of morbid
dosa
and nature of pathology.
Currently, many practitioners use the modern
techniques such as auscultation of the
chest with a stethoscope for confirming the
diagnosis. As there is progress toward holistic
medicine, the Ayurvedic practitioners will
benefit from the advances made in the diagnosis
of asthma.
In modern medicine, the diagnosis can often
be made convincingly on the basis of
clinical history and physical examination.
However, the examination of respiratory system
may be normal as the symptoms are variable. A
physical examination is more likely to
be fruitful if the individual is examined in
the symptomatic period.
Measurement of pulmonary function has an
important place in diagnosis especially if
history and physical examination are
inconclusive. In addition, there can be inaccuracies
in assessment of severity of symptoms by both
patient and physician.
Measurement of airflow limitation (such as
peak expiratory flow rate [PEFR] and forced
expiratory volume [FEV
1
]) and its reversibility are important in
establishing a clear diagnosis
of asthma. Newer guidelines recommend serial
measurements for monitoring the course of
asthma. The tests can be performed with ease
in individuals older than 5 years.
On the basis of the symptomatology and the
result of spirometry, asthma can be
classified into intermittent, mild
persistent, moderate persistent, and severe persistent
types (Table 13.1).
13.7 Clinical Course and Prognosis
According to Ayurveda, of all the significant
svasa
disorders,
tamaka svasa
(asthma) is
yapya
(i.e., controllable).
1
It is not curable and symptoms are likely to
persist. The only exceptions
to this may be disease of short duration in
strong, healthy, young individuals and if the
disease severity is mild.
In the past few decades, a lot of research
has been conducted to determine the natural
history of asthma. Asthma symptoms may
disappear in one third to one half of children
at puberty.
38,39
Even though symptoms may be absent,
abnormalities in lung function can
be demonstrated. However, symptoms may appear
later in adulthood. Nearly two thirds
of children continue suffering from the
disorder through adolescence and adulthood.
Asthma may have onset in adult life.
40
The exact proportion of such patients is not
known. It is likely that exposure to
allergens and development of atopy later in life are
responsible for late onset of asthma. The
role of viral infections in causation in adults is
not clear; they may be a trigger for acute
exacerbation.
The overall description of the prognosis of
asthma in Ayurveda and the current practice
appear to be similar.
13.8 Management
13.8.1 Ayurvedic Approach
Management of asthma in Ayurveda judiciously
encompasses herbal and herbomineral
drugs in addition to advising a healthy
lifestyle and diet that are contrary to the cause of
disease and the disease itself. As the
pathogenesis of this disorder involves an imbalance
between the
vata
and
kapha
, the therapy is directed at correcting this
imbalance. In addition,
there are a few therapies for controlling the
acute symptoms.
The texts recommend that the patients should
be given sudation and steaming therapy
(
svedana
) after anointing their bodies with oils
processed with salt.
2–5
With this method,
the solidified phlegm (
kapha
) adhering inside the channels gets liquefied
and comes into
the alimentary tract. The channels become
soft and
vata
attains its normal downward
TABLE 13.1
Classification of Asthma According to
Severity
Severity Symptoms Nighttime Symptoms PEFR
Severe persistent Continuous, limited
physical activity Frequent
£
60% predicted;
variability >30%
Moderate persistent Daily use of beta-2
agonist, daily
attack affects activity
>One time/week >60–80% predicted;
variability >30%
Mild persistent >One time/week but <
one time/
day
>Two times/month
≥
80% predicted;
variability 20–30%
Intermittent <One time/week, asymptomatic
and
normal PEFR between attack
£
Two times/month
≥
80% predicted;
variability <20%
movement. After sweating, the patient is
advised to eat food rich in fats and food that
improves the secretion of mucus. In order to
eliminate the pathological
kapha
, a therapeutic
emesis is induced with herbs such as
Piper longum
(
pippali
). With this, channels are cleared
and
vata
moves without any hindrances. Purgation
therapy (v
irechana
) may also help in
a few patients. Because of the nature of
these therapies, they should be avoided in young
children and pregnant women.
The purification (
shodhan
) can also be achieved by a more elaborate
process:
panchakarma
.
Panchakarma
involves therapeutic vomiting and emesis (vamana), purgation (virechan),
enema (basti),
elimination of toxins through the nose (nasya),
and purification of the blood
(rakta mokshana). Rakta mokshana may be useful in patients with allergies.
This purification
therapy should not be performed in
debilitated individuals, the elderly, young children,
pregnant women, and frail women.
Various medications are described in
Ayurveda.2–5 These include single drugs and com-
5,41 Some of them are listed below the table.
1. Krsnadi churna — Powder of Piper
longum (pippali), Emblica officinalis (amlaka), and
Zingiber officinalis (sunthi) with honey and sugar added
2. Bharangyadi churna — nagaradi churna — Powder
of bharangi (Clerodendrum serratum)
and sunthi (Zingiber officinalis) with hot water or powder of sunthi, sugar, and
sauvarcala
3. Srangydi churna — Pistacia chinensis (karkatasrngi), trikatu (combination of ginger
root, pippali berry, black pepper), triphala (combination of Emblica officinalis, Terminalia
chebula, and Terminalia bellirica),
Solanum xanthocarpum (kantakari), Clerodendrum
serratum (bharangi), Inula racemosa (puskarmula), and five salts
4. Parnasapancaka — Decoction of Tinospora
cordifolia (guduci), Zingiber officinalis
(sunthi), Rivea hypocrateriformis (phanji), Solanum xanthocarpum (kantakari), and Ocimum
sanctum (parnasa, tulsi) mixed
with Piper longum (pippali) powder
5. Decoction of dasamula (a combination of ten roots: shonyaka, patala, kasmari, agnimantha,
brhati, mahabalam, guduci, kakoli, ananta) added with Inula racemosa (puskaramula)
6. Decoction of Dolichos biflorus (kulattha), Zingiber officinalis (sunthi), Solanum xanthocarpum
(kantakari), and Adhatoda
vasica (vasa) added with Inula
racemosa (puskuramala)
7. Use of jaggery with equal mustard oil
8. Powder of Pistacia chinensis (karkatasrngi), Zingiber officinalis (sunthi), Piper longum
(pippali), Cyperus rotundus (musta),
Inula racemosa (puskarmula), Hedychium spicatum
(sati),
Piper nigrum (marica), and sugar taken with a decoction of Tinospora cordifolia
(guduci), Adhatoda vasica (vasa),
and pancamulla
9. Linctus made from Curcuma longa (haridra), Piper nigrum (marica), Vitis vinifera
(draksa), jaggery, Pluchea
lanceolata (rasna), Piper longum (pippali), and Hedychium
spicatum (sati)
10. The powder of Terminalia bellirica (bibhitaka) fruit mixed with honey
11. Preparation made from ghee, milk, and the
paste of Capparis
sepiaria (himsra);
Embelia ribes (vidanga), Mentha spicata (putika); trikatu; triphala; and Plumbago
zeylanica
(citraka)
12. Preparation made from ghee and paste of tegovati, Terminalia chebula (haritaki),
Piper longum (pippali), Strychnos potatorum (katuka), bhutika, Inula racemosa (puskara-
pound formulations (see Tables 13.2 and 13.3).
mula), Butea monosperma (palasa), Plumbago zeylanica (citraka), Hedychium spicatum
(sati),
sauvarcala, Cinnamomum tamala (tamalaki), rock salt, Aegle marmelos (bilva),
Abies webbiana (talisapatra), Leptadenia reticulata (jivanti), Acorus calamus (vaca),
and
Ferula foetida (hinga)
13. Preparation made from Clerodendrum serratum (bharangi) and dasamula, Terminalia
chebula (haritaki),
jaggery, honey, trikatu, and trijata (powdered) and yavakasra
14. Preparation made from Dolichos biflorus (kulatha), dasamula, Clerodendrum serratum
(bharangi), jaggery, honey, Bambusa arundinacea (vamsalocana), Piper longum (pippali),
and trijata
The above medications are likely to have both
therapeutic and preventive effects. It is
advised to continue any of these for a
prolonged duration.
TABLE 13.2
Single Drugs Used in Ayurvedic Anti-Asthmatic
Preparations
Adhatoda vasica
Aegle marmelos
Alangium salviifolium
Aquilaria agallocha
Arsenic rubrum
Benincasa hispida
Bhasma of horn of stag
Boerhavia diffusa
Calotropis procera
Cedrus deodara
Garcinia pedunculata
Clerodendrum serratum
Curcuma longa
Curcuma zedoria
Datura stramonium
Dolichos biflorus
Elettaria cardamomum
Fagonia cretica
Ferula narthex
Glycyrrhiza glabra
Gypsum
Honey
Inula racemosa
Jaggery
Leptadenia reticulata
Mica
Mucuna pruriens
Ocimum sanctum
Phyllanthus embica
Phyllanthus urinaria
Piper longum
Piper nigrum
Rhus succedanea
Solanum xanthocarpum
Terminalia bellirica
Vitis vinifera
White arsenic
Source: Modified from Goyal, H.R., Tamaka Shwasa (Bronchial Asthma): A
Clinical Study, Central Council for Research in Ayurveda
and Siddha, New
Delhi, 1997.
For controlling acute symptomatology,
inhalation of medicated smoke from the following
preparations have been described in
Ayurveda2–4:
1. Inhalation of the smoke of the fruit, the
stem, and leaves of Dhatura
fastuosa from
a hooka.
A paper dipped in water in which saltpetre has been dissolved is dried
in the sun and rolled up in the form of a
cigar.
2. Paste of Cedrus deodara, Sida cordifolia, and Nardostachys jatamansi is dried in sun,
laced in ghee. Patient inhales the smoke from
a hollow stick made out of this.
3. Leaves of haridra, root of Ricinus communis (eranda), Cocculus lack (laksa), Psidium
guajava (manassial), Cedrus deodara (devadaru), Elettaria cardamomum (ela),
and mamsi
are all macerated and made into cigarette,
which is smeared with ghee and
smoked.
After alleviating the intensity of asthmatic
breathing, the following syrups may be used:
1. Peacock feathers are reduced to ashes in a
slow fire. They are mixed with a quantity
of fruit of Piper longum reduced to powder. A syrup is then made with the aid of
honey. If licked occasionally, it alleviates
the intensity of asthmatic breathing.
2. Turmeric (Curcuma longa), black pepper (Piper nigrum), Uvoe passae, old molasses,
Vanda roxburghii, Piper longum, and Circuina
zerumbet are
reduced to a powder and
mixed with mustard oil.
3. A decoction of Tinospora cordifolia, dry ginger, Siphonanthus indica, Solanum xanthocarpum,
and Ocimum sanctum mixed with powdered Piper longum is made.
TABLE 13.3
Compound Preparations for the Management of
Asthma
Name Instructions
Eladi churn 1–3 with 4–6 g of honey twice/day
Sitopalidi churn 1–3 with 4–6 g of honey twice/day
Srangydi churn 1–3 with 4–6 g of honey twice/day
Talisadi churn 1–3 with 4–6 g of honey twice/day
Dashmula kvath 14–28 ml twice/day
Kantaryadi kvath 14–28 ml twice/day
Srmgyadi kvath 14–28 ml twice/day
Vasadi kvath 14–28 ml twice/day
Agastya haritiki avaleha 12–24 g twice/day
Chavanprash avaleha 12–24 g twice/day
Chitraka haritiki avaleha 12–24 g twice/day
Vasa avaleha 12–24 g twice/day
Vyaghriharitiki avaleha 12–24 g twice/day
Draksharishta 14–28 ml with equal quantity of water
twice/day after meals
Vasarishta 14–28 ml with equal quantity of water twice/day after
meals
Kanakasva 5–10 ml with equal quantity of water twice/day after
meals (due to its
potency, caution is advised)
Abhraka bhasma (plain) 120–150 mg with honey twice/day
Maygrapuccha bhasma 1–2 g with honey twice/day
Apamarga ksara 1 g with warm water twice/day
Arka lavana 1 g with warm water twice/day
Khadiradi vati 2–4 vati three times/day
Lavangadi vati 1 vati six times/day
Source: Modified from Swas
roga, in Handbook of Domestic Medicine and Common
Ayurvedic Remedies, Central
Council for Research in Ayurveda and Siddha,
1999. These preparations may be obtained from major
Ayurvedic pharmaceutical companies in India.
4. Parnasapancaka — A decoction of guduci,
sunthi, phanji, kantakari, and
parnasa (tulsi)
mixed with pippali powder is made.
5. A syrup made out of Curcuma zedoria (kachur), Inula racemosa (pushkarmool), Citrus
decumona (amla vetas), Elettaria cardamomum (choti Elaichi), Ferula narthex (hingu),
Ocimum sanctum (tulsi),
Aquilaria agallocha (agar),
Phyllanthus urinaria (bhumyamalki),
Leptadenia reticulata (jeewanti), and Santalum
album (chanda) is recommended
as a bronchial antispamodic.
Although inhaling the smoke of various herbs
may cause relief through the bronchodilatory
effect of the constituents such as dhatura, this practice has not been evaluated
scientifically to recommend its routine
usage. In addition, the smoke may actually worsen
the bronchospasm. This form of therapy is
neither feasible in children nor advisable.
13.8.1.1 Precautions
The drugs, diet, and practices that aggravate
the disease should be avoided. These include
dust, smoke, residing in cold places,
excessive use of cold water, seasonal changes, excessive
walking, excessive use of dry foods,
astringent food, irregular dietary habits, indigestion,
trauma to vital organs, and habitual use of lablab-bean, black gram, til paste, and
other kapha-producing
articles.
13.8.1.2 Diet
Foods and drinks that restore the normal
course of vata are useful in treating asthma. If
the vata is
greatly excited, syrup made up from old tamarind pulp is helpful. Sugar candy
with lemon (Citrus medica) juice is beneficial. Light foods should be eaten at night. Heavy
and rich foods, which are difficult to
digest, foods that are dry, curds, fish, and chillies
should all be avoided.
13.8.1.3 Lifestyle
Staying awake at night, exercising, labor,
exposing oneself to the heat of the sun or fire,
and anxieties, grief, wrath, and everything
that disturbs peace of mind should be avoided.
A healthy lifestyle would have a preventive
role.
13.8.1.4 Breathing Exercises
Breathing exercises, particularly pranayam, reduce the frequency and severity of symptoms,
42–44 improve exercise tolerance, and enhance
lung function. Two systematic reviews
have highlighted the need for studying the
beneficial aspects of various breathing exercises.
45,46
13.8.1.5 Meditation
Meditation helps in reducing the stress and
may check recurrence. Sahaja yoga is an Indian
system of meditation based on traditional
yogic principles, which may be used for therapeutic
purposes. Clinical trials of this therapy in
patients with asthma have found evidence
of improvement in lung function and reduced
frequency of exacerbations.47
Some commercial Ayurvedic formulas are also
available that may be useful in asthma.
Examples include Asmon (Herbochem Remedies,
Kolkata) and Asmakure (Herbicure Pvt.
Ltd., Bishanpur, West
Bengal).
13.8.2 Conventional Medicine Approach
There is no cure available for asthma in
Western medicine. However, appropriate management
leads to control of the disorder. The goals
of management are to:
1. Control the symptoms.
2. Prevent acute exacerbations.
3. Maintain normal or near normal pulmonary
functions.
4. Maintain normal levels of activity.
5. Avoid adverse effects from medications.
6. Prevent mortality due to asthma.
Currently, therapy of asthma is guided by the
fact that it is a chronic inflammatory
airway disorder; the control of airway
inflammation is the key to effective control. Except
for mild intermittent asthma, the therapy
includes regular use of anti-inflammatory medication
and bronchodilators (as required). In
addition, environmental control to avoid
exposure to certain risk factors should
improve the control of symptoms.
The first step in management after the
diagnosis is made is the correct assessment of
The pharmacological therapy of bronchial
asthma involves the use of drugs that relax
smooth muscle and dilate the airways and
drugs that decrease inflammation and prevent
exacerbations. The medications used for
long-term treatment of asthma include bronchodilators,
steroids, mast-cell stabilizers, leukotriene
modifiers, and theophylline.48–75
alone in persistent asthma is not
recommended, as this does not control the airway
inflammation and there is a false sense of
security.
13.8.2.1 Immunotherapy
This therapeutic mode consists of gradually
giving increasing quantities of an allergen
extract to a clinically sensitive subject to
ameliorate the symptoms associated with subse-
TABLE 13.4
Stepwise Treatment of Asthma
Steps Long-Term Prevention
Step 4: Severe
persistent
Inhaled short-acting beta-agonist as
required; inhaled corticosteroids:
Budesonide and Beclomethasone (400 mg twice/day) increase up to
2000 mg/day in selected cases;
long-acting bronchodilator: long-acting
inhaled b2-agonist or sustained release
theophylline; corticosteroids
tablets: low dose on alternate days (if no
relief with above treatment)
Step 3: Moderate
persistent
Inhaled short-acting beta-agonist as
required; inhaled corticosteroids:
Budesonide and Beclomethasone (400–800 mg divided twice/day);
long-acting bronchodilator (if needed):
long-acting inhaled b2-agonist
salmeterol (50 mg once or twice/day or
sustained release theophylline)
Step 2: Mild
persistent
Inhaled short-acting b-agonist as required; inhaled corticosteroids:
Budesonide and Beclomethasone (200–400 mg) or cromolyn or
sustained release theophylline or leukotriene
modifiers
Step 1: Intermittent Inhaled short-acting b-agonist as required for symptoms relief; if they
are needed more than three times/week, move
to step 2
Note: If Fluticasone is used, the dose is half that of
Budesonide/Beclomethasome.
severity of asthma (Table 13.1).
Table
13.4 shows the treatment plan according to
disease severity. The use of bronchodilators
quent exposure to a causative allergen. This
is considered only occasionally in highly
selected children who are sensitive to a
specific allergen such as grass pollen, mites, etc.
It is done only under specialist supervision
and must usually be given for 3 years.76 Some
studies suggest that specific immunotherapy
may induce a diminution of nonspecific
bronchial hyperresponsiveness and enable
reduction of symptomatic treatment.77,78
13.8.2.2 Management of Acute Exacerbation
Severe exacerbations of asthma are
life-threatening medical emergencies requiring hospitalbased
care. The aims of treatment are to reverse
airflow obstruction and hypoxemia as
rapidly as possible. The severity of an acute
exacerbation can be judged by clinical symptoms
and signs, lung function tests, and arterial
blood gas analysis. Rapid-acting inhaled
bronchodilators, early introduction of
systemic glucocorticoids, and supplemental oxygen
are the mainstay of treatment of acute
exacerbations. Close monitoring of the patient’s
condition and response to therapy are
mandatory. In addition, a plan should be formulated
to prevent future relapses.
13.8.2.3 Complications of Therapy
Use of systemic (oral, parenteral) steroids
over a prolonged period is associated with
significant side effects. However, the
current day management relies more on inhalation
drugs. The main concern with the use of
inhalation steroids is the effect on growth. An
approximate 20% reduction in the growth
velocity during the first year of treatment with
inhaled steroids is reported. Subsequently,
the growth velocity recovers and children
ultimately attain predicted adult
height.56,57 Studies have also reported that children treated
with inhaled steroids were more likely to
reach predicted adult height than children whose
asthma was not treated with preventive
medication.57,58 These findings show that the
concern about adverse effect of inhaled
steroids on growth is inappropriate.
The complications associated with beta-2
agonists are cardiovascular stimulation, skeletal
muscle tremor, hypokalemia, and irritability.
These adverse effects are more commonly
seen with oral drugs than with inhaled
medications.
If asthma severity is assessed properly and
inhaled medications are used judiciously,
the benefits far outweigh the risks.
13.9 Scientific Basis
4
41 There is a
great deal of scientific literature available
that supports the use of Ayurvedic preparations
in the management of asthma. Most of the data
are experimental. These studies highlight
the anti-inflammatory and bronchodilatory
activity in various medications. The following
list shows the evidence available for various
herbs:
1. Picrorrhiza kurroa — P. kurroa is a
widely used herb in the Ayurvedic system. It
belongs to the Scrophulariaceae family, and
the active constituents are obtained
from the root and rhizomes.79 It is
traditionally used in treatment of respiratory
conditions such as asthma and bronchitis.
Studies on an alcoholic extract have
shown antioxidant and anti-inflammatory
effects.80 In animal studies, antiallergic,
A large number of single drugs have been
described for use in asthma (Table 13.2). In
addition there are quite a few compound
preparations available (Table 13.3).
© 2004 by CRC Press LLC
Bronchial Asthma 221
antianaphylactic, anti-inflammatory, and immunomodulatory
activities have been
demonstrated. The active ingredients include
pikuroside II, picroliv (containing
iridoid glycoside fraction), and
androsin.81–86
2. Adhatoda vasica — This is widely used in treatment of respiratory tract ailments.
Alkaloids from this herb have been shown to
possess anti-inflammatory and
antiallergic properties.85,87,88 In addition,
its extract has an antitussive effect.89
3. Albizzia lebbek — The decoction of the bark of A. lebbek is used in treatment of
asthma and eczema. Studies on animals show
that A. lebbek has a significant
cromoglycate-like action on the mast cells.
It also appears to inhibit the early
processes of sensitization and synthesis of
reaginic-type antibodies.90,91
4. Solanum species — Powder of or a decoction made from the whole dry plant of
Solanum xanthocarpum or Solanum trilobatum is used in the treatment of asthma
and other respiratory disorders. The
mechanism of action in asthma may involve
bronchodilation, reduction of bronchial
mucosal edema, and reduction of airway
secretions.92–94
5. Tylophora indica — T. indica is widely used in Ayurvedic medications to
provide
relief to patients with bronchial asthma.
Studies have shown that alkaloids of
Tylophora indica suppress cellular immune response.95
6. Cedrus deodara — The wood oil of C.
deodara has been
shown to have anti-inflammatory
activity. This can be attributed to its
mast-cell stabilizing activity and the
inhibition of leukotriene synthesis.96
7. Boswellia serrata — The gum resin of B. serrata contains
boswellic acids which have
been shown to inhibit biosynthesis of
leukotrienes.97
8. Phyllanthus urinaria — The extracts of the stems, leaves, and roots have been
shown
to have a relaxant effect on the respiratory
tract smooth muscle; involvement of
adenosine tri-phosphate- (ATP) sensitive
potassium channels is postulated.98
9. Aquilaria agallocha — Aqueous extracts of stems of A. agallocha have been shown
to inhibit immediate hypersensitivity
reaction by inhibition of histamine release
from mast cells.99
10. Calotropis procera — The latex of Calotropis procera has anti-inflammatory property
demonstrated in a rat paw edema model.100
11. Elettaria cardamomum oil — Anti-inflammatory and antispasmodic properties have
been demonstrated in a study on rats.101
12. Ocimum sanctum — Extracts of this widely used plant have been shown to possess
immunomodulatory potential and antioxidant
and cyclooxygenase inhibitory
properties.102,103 Its fixed oils can inhibit
enhancement of the vascular and capillary
permeability and leukocyte migration after
inflammatory stimulus.104
13. Piper longum — Piperine, isolated from this plant, has anti-inflammatory potential.
105
13.9.1 Review of Clinical Trials
13.9.1.1 Picrorrhiza kurroa
Doshi et al.106 studied the efficacy of P. kurroa in a randomized, crossover, double-blind
trial. They enrolled 72 patients (ages 14 to
60) for a 14-week study. The patients were given
either P. kurroa root powder (300 mg three times/day) or an identical placebo. The study
had three arms: (1) group A had a long
duration of 12 weeks and an active drug was
given from week 3 to week 14, (2) group B had
a short duration of 3 weeks and an active
drug was given from week 3 to week 6 with
placebo during the rest of the period, and
(3) group C had an intermediate duration of 6
weeks and an active drug was given from
week 3–6 and 9–12 with a placebo during
intervening periods. The patients were asked
to maintain a symptom diary. Weekly pulmonary
function tests were performed. The
authors did not observe any significant
reduction in clinical exacerbation, need for bronchodilators,
or improvement in pulmonary function. Fifty
patients dropped out of study
at different points during the trial.
Significant side effects were seen in ten patients — four
experienced vomiting, three had anorexia, two
had diarrhea, two experienced itching, one
had a skin rash, and one experienced
giddiness. As this preparation is used frequently,
there is need for further studies.
13.9.1.2 Solanum spp.
Govindan et al.107 studied the efficacy of
this herb in bronchial asthma. They enrolled 60
adults with bronchial asthma. Twenty patients
each received 300 mg of dry powder of S.
xanthocarpum or S. trilobatum, whereas 10 patients each received salbutamol 4 mg or
deriphylline 200 mg. Pulmonary function tests
were performed before and 2 h after drug
administration. S. xanthocarpum and S. trilobatum increased FEV1 by 65 and 67%, respectively,
at 2 h. This effect was less than that with
salbutamol or deriphylline. Subjective
relief lasted 6 to 8 h.
Similar results have been reported in other
studies as well; the response rates were
poor.108,109 In these studies the duration
for which the drug was given was small; these
results may lead to an underestimation of the
effects because most Ayurvedic herbal
preparations have their best action after
about 2 weeks.
13.9.1.3 Tylophora indica
Shivpuri et al.110 conducted a double-blind,
crossover study in 110 patients over 10 years
old. Fifty-three patients in the control
group ate one spinach leaf daily. At the end of week
1, 62% in the T. indica group had moderate to complete relief of symptoms
compared with
28% in the control group. At the end of the
12-week study period, improvements in the
two groups were 16 and 0%, respectively.
In another double-blind, crossover study,111
195 asthmatic patients received either alcoholic
tincture of T. indica or a placebo for 12 weeks. A daily dairy of symptoms scores was
maintained. After a week, 56% of the patients
in T. indica group had moderate to complete
improvement in symptoms compared with 31.6%
in the placebo group. After the crossover,
34.2% had improved with T. indica and 13.5% with placebo. At the end of study period,
14.8% in the T. indica group and 7.2% in the placebo group improved.
The efficacy of alkaloids extracted from T. indica was studied in a double-blind trial of
123 patients.112 The study group received
alkaloid extract from T.
indica in glucose, whereas
the control group received glucose colored
with spinach. Lung-function tests were evaluated
along with symptom scores. The percentage of
patients in whom FEV1 improved
by more than 15% was significantly greater in
the study group than the control at 1, 2, 4,
8, and 12 weeks, peaking at 4 weeks. The
symptom scores were significantly better in the
study group, with the peak at 1 week.
Thiruvengadam et al.113 studied the efficacy
of dried T.
indica in 30 asthmatic patients.
The patients were enrolled into a four-arm,
double-blind randomized clinical trial for 16
days. Dried T. indica powder was compared with standard drugs and a placebo. Pulmonary
function tests and symptom scores were
evaluated. Among all the parameters, nocturnal
dyspnea was the only one that showed
significant improvement with T. indica.
A placebo-controlled double-blind study114 on
135 asthmatic patients was conducted to
evaluate the efficacy of powdered T. indica. The drug or placebo was given for 1 week
with another 2 weeks of follow-up. Pulmonary
function tests and symptoms scores were
evaluated. There were no differences between the
two groups.
13.9.1.4 Boswellia serrata
The gum resins of B. serrata (salai guggul) have
been used in asthma. Gupta et al.115
compared the effect of gum resins of B. serrata with placebo in a double-blind, randomized
trial on 80 adult asthmatic patients.
Pulmonary function tests were evaluated serially. A
significant increase in FEV1 was reported in
the test group compared with the placebo
group.
13.9.1.5 Miscellaneous Herbs
Iyenger et al.116 studied the effect of a
combination of five plants — Adhatoda vasica, Solanum
xanthocarpum, Albizzia lebbek, Glycyrrhiza
glabra, and Picrorrhiza kurroa — in 14 adult patients
with asthma. All the patients showed clinical
improvement with prevention of recurrence
and reduction in severity of symptoms.
However, the medication was not effective during
acute exacerbation.
Shanker et al.117 conducted a clinical trial
on 15 patients with bronchial asthma using
Gardenia turgida and Gardenia latifola. The results were unimpressive.
Sharma et al.118 reported significant improvement
in one third of the 15 patients they
treated with Euphorbia prostrata for a period of 2 weeks.
Swamy et al.119 evaluated the efficacy of sirisa twak kvatha (Albizzia lebbek) in 19 patients
with asthma. They reported significant
improvement in symptoms in most patients.
Trivedi et al.120 reported bronchodilatory,
antispasmodic, and antiasthmatic effects of
vibhitakphal churna (Terminalia bellirica) in a trial on 93 patients.
In another trial,5 240 cases of bronchial
asthma were administered naradeeya lakshmi vilas
rasa and godanti bhasma in a dose of 0.5 and 1.0 g, respectively,
three times/day with honey
for a varying period of 4 to 12 weeks.
Ninety-six patients received 100% relief, 27 patients
received 75% relief, 50 patients received 50%
relief, 18 cases received 25% relief, and 28
remained unchanged; 21 cases left against
medical advice. In the second group of this
study, 210 cases received shvasa kesari tablets (500 mg) made from Solanum xanthocarpum
and Godanti bhasma three times/day for 2 to 12 weeks. Seventy-five cases showed complete
relief, 49 cases showed 75% relief, 26 cases
showed 50% relief, 25 cases showed 25% relief,
and 24 did not respond to therapy; 10 cases
left against medical advice.
As can be judged from these studies, most
trials have demonstrated some benefit. When
analyzing the available literature and
Ayurvedic texts, we conclude that more clinical
research is still required before these
therapies can be routinely used. Although there are
good experimental data to justify use of Ayurvedic
preparations in asthma, issues about
doses, combinations, and duration of therapy
are still to be resolved. In addition, these
preparations do not seem to offer effective
medications for acute exacerbations of asthma,
which can be life threatening. There are
plenty of Ayurvedic preparations with anti-inflammatory
and immunomodulatory effects (vide supra).
Further research is required to determine
the optimal combinations that will help in
reducing the airway inflammation and
therefore lead to better control of symptoms.
It appears that a judicious mix of Ayurvedic
medications and modern medicine may be able
to improve the control of this common
respiratory disorder.
13.10 Areas of Research
Further research is needed to:
1. Establish efficacy of various Ayurvedic
preparations used in asthma by good
quality randomized controlled trials.
2. Determine the active principles in various
Ayurvedic medications.
3. Evaluate the impact of Ayurvedic
medications on the natural history.
4. Evaluate the role of immunomodulator
medications available in Ayurveda.
13.11 Conclusions
The review of literature highlights need for
more research in utility of Ayurvedic preparations
in bronchial asthma. At present, the
medications and the management are not well
standardized. As a large number of
experimental studies have documented the presence
of anti-inflammatory properties in various
Ayurvedic preparations, there is potential for
discovering new compounds useful in the
management of asthma.
References
1. International Study of Asthma and
Allergies in Childhood (ISAAC) Steering Committee,
Worldwide variation in prevalence of symptoms
of asthma, allergic rhinoconjunctivitis, and
atopic eczema: ISAAC, Lancet, 351, 1225, 1998.
2. Murthy, K.R.S., Astanga Samgraha of Vagbhata, Vol. 2, Chaukhmba Orientalia, Varanasi, 1986,
p. 326.
3. Sharma, P.V., Cakradatta: A Treatise on Principles and
Practices of Ayurvedic Medicine, Chaukhambha
Orientalia, Varanasi, 1994, p. 145.
4. Sengupta, N.N., The Ayurvedic System of Medicine, Vol. 1, Neeraj Publishing, New Delhi, 1984,
p. 198.
5. Goyal, H.R., Tamaka Shwasa (Bronchial Asthma): A Clinical
Study, Central Council for Research
in Ayurveda and Siddha, New Delhi, 1997.
6. Weiss, S.T., Parasites and asthma/allergy:
what is the relationship?, J. Allergy Clin. Immunol.,
105, 205, 2000.
7. Masters, S. and Barrett-Connor, E.,
Parasites and asthma-predictive or protective?, Epidemiol.
Rev., 7, 49, 1985.
8. Haahtela, T., Lindholm, H., Bjorksten, F.,
et al., Prevalence of asthma in Finnish young men,
Br. Med. J., 301, 266, 1990.
9. Veale, A.J., Peat, J.K., Tovey, E.R., et
al., Asthma and atopy in four rural Australian aboriginal
communities, Med. J. Aust., 165, 192, 1996.
10. European Community Respiratory Health
Survey (ECRHS), Variations in the prevalence of
respiratory symptoms, self-reported asthma
attacks, and use of asthma medication in the
European Community Respiratory Health Survey
(ECRHS), Eur.
Respir. J., 9, 687,
1996.
11. Devereux, G., Ayatollahi, T., Ward, R.,
et al., Asthma, airways responsiveness and air pollution
in two contrasting districts of northern England, Thorax, 51, 169, 1996.
12. Burney, P.G., Luczynska, C., Chinn, S.,
et al., The European Community Respiratory Health
Survey, Eur. Respir. J., 7, 954, 1994.
13. Asher, M.I., Keil, U., Anderson, H.R., et al., International Study
of Asthma and Allergies in
Childhood (ISAAC): rationale and methods, Eur. Respir. J., 8, 483, 1995.
14. Beasley, C.R.W., Pearce, N.E., and Crane,
J., Worldwide trends in asthma mortality during the
twentieth century, in Fatal Asthma, Sheffer, A.L., Ed., Marcel Dekker, New York, 1998, p. 13.
15. Holgate, S.T., Genetic and environmental
interaction in allergy and asthma, J. Allergy Clin.
Immunol., 104, 1139, 1999.
16. Wiesch, D.G., Meyers, D.A., and Bleecker,
E.R., Genetics of asthma, J. Allergy Clin. Immunol.,
104, 895, 1999.
17. Gissler, M., Jarvelin, M.R., Louhiala,
P., et al., Boys have more health problems in childhood
than girls: follow-up of the 1987 Finnish
birth cohort, Acta
Paediatr., 88,
310, 1999.
18. Sears, M.R., Burrows, B., Flannery, E.M.,
et al., Atopy in childhood. I. Gender and allergen
related risks for development of hay fever
and asthma, Clin.
Exp. Allergy, 23,
941, 1993.
19. Platts-Mills, T.A., Role of allergens in
asthma and airway hyperresponsiveness: relevance to
immunotherapy and allergen avoidance, in Asthma: Its Pathology and Treatment, Kaliner, M.A.
and Persson, C.G., Eds., Marcel Dekker, New York, 1991.
20. Sporik, R., Holgate, S.T., Platts-Mills,
T.A., et al., Exposure to house-dust mite allergen (Der
p I) and the development of asthma in
childhood: a prospective study, N. Engl. J. Med., 323,
502, 1990.
21. Pearce, N., Douwes, J., and Beasley, R.,
Is allergen exposure the major primary cause of
asthma?, Thorax, 55, 424, 2000.
22. Lau, S., Illi, S., Sommerfeld, C., et
al., Early exposure to house-dust mite and cat allergens and
development of childhood asthma: a cohort
study, Multicentre Allergy Study Group, Lancet,
356, 1392, 2000.
23. Gold, D.R., Environmental tobacco smoke,
indoor allergens, and childhood asthma, Environ.
Health Perspect., 108(Suppl. 4), 643, 2000.
24. Jones, A.P., Asthma and the home
environment, J.
Asthma, 37, 103, 2000.
25. Johnston,
S.L., Viruses and asthma, Allergy, 53,
922, 1998.
26. Gern, J.E., Viral and bacterial
infections in the development and progression of asthma, J.
Allergy. Clin. Immunol., 105, S497, 2000.
27. Sigurs, N., Bjarnason, R., Sigurbergsson,
F., et al., Respiratory syncytial virus bronchiolitis in
infancy is an important risk factor for
asthma and allergy at age 7, Am. J. Respir. Crit. Care
Med., 161, 1501, 2000.
28. Keeley, D.J., Neill, P., and Gallivan,
S., Comparison of the prevalence of reversible airways
obstruction in rural and urban Zimbabwean
children, Thorax, 46, 549, 1991.
29. Sandberg, S., Paton, J.Y., Ahola, S., et
al., The role of acute and chronic stress in asthma attacks
in children, Lancet, 356, 982, 2000.
30. Vignola, A.M., Chanez, P., Campbell, A.M., et al.,
Airway inflammation in mild intermittent
and in persistent asthma, Am. J. Respir. Crit. Care Med., 157, 403, 1998.
31. Bousquet, J., Chanez, P., Lacoste, J.Y.,
et al., Eosinophilic inflammation in asthma, N. Engl. J.
Med., 323, 1033, 1990.
32. Bousquet, J., Jeffery, P.K., Busse, W.W.,
et al., Asthma: from bronchoconstriction to airways
inflammation and remodeling, Am. J. Respir. Crit. Care Med., 161, 1720, 2000.
33. Lampinen, M., Rak, S., and Venge, P., The
role of interleukin-5, interleukin-8 and RANTES in
the chemotactic attraction of eosinophils to
the allergic lung, Clin. Exp.
Allergy, 29, 314, 1999.
34. Humbert, M., Menz, G., Ying, S., et al.,
The immunopathology of extrinsic (atopic) and intrinsic
(non-atopic) asthma: more similarities than
differences, Immunol.
Today, 20, 528, 1999.
35. Chung, K.F. and Barnes, P.J., Cytokines
in asthma, Thorax, 54, 825, 1999.
36. Dunnill, M.S., The pathology of asthma
with special reference to changes in the bronchial
mucosa, J. Clin. Pathol., 13, 27, 1960.
37. Wenzel, S.E., Szefler, S.J., Leung, D.Y.,
et al., Bronchoscopic evaluation of severe asthma:
persistent inflammation associated with high
dose glucocorticoids, Am. J.
Respir. Crit. Care
Med., 156, 737, 1997.
38. Kelly, W.J., Hudson,
I., Raven, J., et al., Childhood asthma and
adult lung function, Am. Rev.
Respir. Dis., 138, 26, 1988.
39. Martin, A.J., Landau, L.I., and Phelan,
P.D., Asthma from childhood at age 21: the patient and
his disease, Br. Med. J. (Clin. Res Ed.), 284, 380, 1982.
40. Lange, P., Prognosis of adult asthma, Monaldi. Arch. Chest. Dis., 54, 350, 1999.
41. Central Council for Research in Ayurveda
and Siddha (CCRAS), Handbook
of Domestic Medicine
and Common Ayurvedic Remidies, Ministry of Health and Family Welfare,
Government of India,
New
Delhi,
Documentation and Publication Division, CCRAS, 61-65 Institutional Area,
Janakpuri,
New
Delhi,
1999, chap. Swasa roga.
42. Vedanthan, P.K., Kesavalu, L.N., Murthy,
K.C., et al., Clinical study of yoga techniques in
university students with asthma: a controlled
study, Allergy Asthma Proc., 19, 3, 1998.
43. Jain,
S.C. and Talukdar, B., Evaluation
of yoga therapy programme for patients of bronchial
asthma, Singapore Med. J., 34, 306, 1993.
44. Singh, V., Wisniewski, A., Britton, J.,
et al., Effect of yoga breathing exercises (pranayama) on
airway reactivity in subjects with asthma, Lancet, 335, 1381, 1990.
45. Ernst, E., Breathing techniques:
adjunctive treatment modalities for asthma? A systematic
review, Eur. Respir. J., 15, 969, 2000.
46. Holloway, E. and Ram, F.S., Breathing
exercises for asthma, Cochrane
Database Syst. Rev., 3,
CD001277, 2000.
47. Manocha, R., Marks, G.B., Kenchington,
P., et al., Sahaja yoga in the management of moderate
to severe asthma: a randomised controlled
trial, Thorax, 57, 110, 2002.
48. Lenney, W., Boner, A.L., Ebbutt, A., et
al., Efficacy and safety of salmeterol in childhood asthma,
Eur. J. Pediatr., 154, 983, 1995.
49. Blake, K., Pearlman, D.S., Scott, C., et
al., Prevention of exercise induced bronchospasm in
pediatric asthma patients. Comparision of
Salmeterol powder with salbutamol, Ann. Allergy
Asthma Immunol., 82, 205, 1999.
50. Greening, A.P., Ind,
P.W., Northfield,
M., et al., Added salmeterol versus higher dose corticosteroids
in asthma patients with symptoms on existing
inhaled corticosteroids, Lancet, 344,
219, 1994.
51. Bartow, R.A. and Brogdem, R.N.,
Formeterol: an update of its pharmacologic properties and
therapeutic efficacy in the management of
asthma, Drugs, 55, 303, 1998.
52. Mitchell, J.A., Belvisi, M.G., Mon, R.A.,
et al., Induction of cyclooxygenase 2 by cytokines in
human pulmonary epithelial cells regulation
by dexamethasone, Br. J.
Pharmacol., 113,
1008,
1994.
53. Scarfone, R.J., Fuchs, S.M., Nager, A.L.,
et al., Controlled trial of oral prednisone in the
emergency department treatment of children
with acute asthma, Pediatrics,
92, 513, 1993.
54. Dahl, R. and Johansson, S.A.,
Importance of duration of treatment with inhaled budesonide
on the immediate and late bronchial reaction,
Eur. Respir. J., 63(Suppl. 122), 167, 1998.
55. Ferguson,
A.C., Spier, S., Manjra, A., et al., Efficacy and safety of high-dose inhaled
steroids
in children with asthma: a comparison of
fluticasone propionate with budesonide, J. Pediatr.,
134, 422, 1999.
56. Agertoft, L. and Pedersen, S., Effect of
long-term treatment with inhaled corticosteroids on
growth and pulmonary function in asthmatic
children, Respir.
Med., 88, 373, 1994.
57. Agertoft, L. and Pedersen, S., Effect of
long-term treatment with inhaled budesonide on adult
height in children with asthma, N. Engl. J. Med., 343, 1064, 2000.
58. The Childhood Asthma Management Program
Research Group, Long-term effect of budesonide
or nedocromil in children with asthma, N. Engl. J. Med., 343, 1054, 2000.
59. Allen, D.B., Mullen, M.C., and Mullen,
B., A meta analysis of the effect of oral and inhaled
corticosteroid on growth, J. Allergy Clin. Immunol., 93, 967, 1994.
60. Szefler, S.J., A review of Budesonide
inhalation suspension in the treatment of pediatric
asthma, Pharmacotherapy, 21, 195, 2001.
61. Furukawa, C.T., Shapiro, G.G., Bierman,
C.W., et al., A double blind study comprising the
effectiveness of cromolyn and sustained
release theophylline in childhood asthma, Pediatrics,
74, 453, 1984.
62. Croce, J., Negreiros, E.B., Mazzei, J.A.,
et al., A double blind, placebo-controlled comparison
of sodium cromoglycate and ketotifen in the
treatment of childhood asthma, Allergy, 50, 524,
1995.
63. Yasuhiro, K., Kae, M., Michiko, F., et
al., Disodium cromoglycate use in children and adolescents
with asthma: correlation between plasma
concentrations and protective effects for various
inhalation methods, Ann. Allergy Asthma Immunol., 83, 553, 1999.
64. de Benedictis, F.M., Tuteri, G.,
Bertotto, A., et al., Comparison of the protective effects of
cromolyn sodium and nedocromil sodium in the
treatment of exercise induced asthma in
children, J. Allergy Clin. Immunol., 94, 684, 1994.
65. Cherniack, R.M., Wasserman, S.I.,
Ramsdell, J.W., et al. A double blind multicentre group
comparative study of the efficacy of
nedocromil sodium in management of asthma, Chest, 101,
1292, 1990.
66. Childhood Asthma Management Program
Research Group, Long-term effects of budesonide
or Nedocromil in children with asthma, N. Engl. J. Med., 343, 1054, 2000.
67. Kabra, S. K., Pandey, R.M., Singh, R., et
al., Ketotifen for asthma in children aged 5 to 15 years:
a randomized placebo-controlled trial, Ann. Allergy Asthma Immunol., 85, 46, 2000.
68. Legg, J. and Warner, J., Asthma: the
changing face of drug therapy, Indian J. Pediatr., 67, 147,
2000.
69. Romanet, S., Stremler-Lebel, N., Magnan,
A., et al., Role of leukotriene inhibitors in the
treatment of childhood asthma, Arch. Pediatr., 7,969, 2000.
70. Weisberg, S.C., Pharmacotherapy of asthma
in children, with special reference to leukotriene
receptor antagonists, Pediatr. Pulmonol., 29, 46, 2000.
71. Knorr, B., Holland, S., Rogers, J.D., et
al., Montelukast adult (10-mg film-coated tablet) and
pediatric (5-mg chewable tablet) dose
selections, J.
Allergy Clin. Immunol., 106
(Suppl. 3), S171,
2000.
72. Kemp, J.P., Dockhorn, R.J., Shapiro, G.G.,
et al., Montelukast once daily inhibits exerciseinduced
bronchoconstriction in 6 to 14-year old
children with asthma, J.
Pediatr., 133, 424,
1998.
73. Berkowitz, R., Schwartz, E., Bukstein,
M.D., et al., Albuterol protects against exercise-induced
asthma longer than metaproterenol sulfate, Pediatrics, 77, 173, 1986.
74. Green, C.P. and Price, J.F., Prevention
of exercise-induced asthma by inhaled salmeterol xinafoate,
Arch. Dis. Child., 67, 1014, 1992.
75. Knorr, B., Matz, J., Bernstein, J., et
al., Montelukast for chronic asthma in 6-to 14-year-old
children. J.A.M.A., 279, 1181, 1998.
76. Bousquet, J., Hejjaove, A., and Michel,
F.B., Specific immunotherapy in asthma, J. Allergy Clin.
Immunol., 86, 292, 1990.
77. Pichler, C.E., Helbling, A., and Pichler,
W.J., Three years of specific immunotherapy with
house-dust-mite extracts in patients with
rhinitis and asthma: significant improvement of
allergen-specific parameters and of
nonspecific bronchial hyperreactivity, Allergy, 56, 301, 2001.
78. Pajno, G.B., Morabito, L., Barberio, G.,
et al., Clinical and immunological effect of long term
sublingual immunotherapy in asthmatic
children sensitized to mites: a double blind, placebocontrolled
study, Allergy, 55, 842, 2000.
79. Anon., Picrorrhiza kurroa, monograph, Altern. Med. Rev., 6, 319, 2001.
80. Russo, A., Izzo, A.A., Cardile, V., et
al., Indian medicinal plants as antiradical and DNA
cleavage protectors, Phytomedicine, 8, 125, 2001.
81. Jia, Q., Hong, M.F., and Minter, D.,
Pikuroside: a novel iridoid from Picrorrhiza kurroa, J. Nat.
Prod., 62, 901, 1999.
82. Baruah, C.C., Gupta, P.P., Nath, A., et
al., Anti-allergic and anti-anaphylactic actively of
picroliv-a standardized iridoid glycoside
fraction of Picrorrhiza kurroa, Pharmacol. Res., 38,
487, 1998.
83. Simons, J.M., Haart, L.A., Van Dijk, H., et al., Immunomodulatory
compounds from Picrorrhiza
kurroa: isolation and characterization of two
anti complementary polymeric fractions
from an aqueous root extract. J. Ethnopharmacol., 26, 169, 1989.
84. Dorsch, W., Stuppner, H., Wagner, H., et
al., Anti asthmatic effects of Picrorrhiza kurroa:
androsin prevents allergen and PAF induced
bronchial obstruction in guinea pigs, Int. Arch.
Allergy Appl. Immunol., 95, 128, 1991.
85. Dorsch, W. and Wagner, H., New antiasthmatic
drugs from traditional medicine?, Int. Arch.
Allergy Appl. Immunol., 94, 262, 1991.
86. Mahajani, S.S. and Kulkarni, R.D., Effect
of disodium cromoglycate and Picrorrhiza kurroa
root powder on sensitivity of guinea pigs to
histamine and sympathomimetic amines, Int.
Arch. Allergy Appl. Immunol., 53, 137, 1977.
87. Claesan, U.P., Malmfors, T., Wikman, G.,
et al., Adhatoda vasica: a critical review of
ethnopharmacological and toxicological data, J. Ethnopharmacol., 72, 1, 2000.
88. Gupta, O.P., Sharma, M.L., Ghatak, B.J.,
et al., Pharmacological investigations of vasicine and
vasicinone – the alkaloids of Adhatoda
vasica, Indian J. Med. Res., 66, 680, 1977.
89. Dhuley, J.N., Antitussive effect of
Adhatoda vasica extract on mechanical or chemical stimulation-
induced coughing in animals, J. Ethnopharmacol., 67, 361, 1999.
90. Tripathi, R.M., Sen, P.C., and Das, P.K.,
Studies on the mechanism of action of Albizzia lebbek,
an Indian indigenous drug used in the
treatment of atopic allergy, J. Ethnopharmacol., 1, 385,
1979.
91. Tripathi, R.M. and Das, P.K., Studies on
antiasthmatic and anti-anaphylactic activities of
Albizzia lebbek, Indian J. Pharmacol., 9, 189, 1977.
92. Gupta, S.S. and Gupta, N.K., Effect of
Solanum xanthocarpum and Clerodendron serratum
on histamine release from tissues, Indian J. Med. Sci., 21, 795, 1967.
93. Gupta, S.S., Verma, S.C.,
Singh, C., et al., Chemical and pharmacological studies on Solanum
xanthocarpum (Kantakari) in chronic
bronchitis, bronchial asthma and non-specific unproductive
cough, Indian J. Med. Res., 55, 723, 1967.
94. Bector, N.P. and Puri, A.S., Solanum
xanthocarpum (Kantakari) in chronic bronchitis, bronchial
asthma and non specific unproductive cough, J. Assoc. Phy. India, 19, 741, 1971.
95. Ganguly, T. and Sainis, K.B., Inhibition
of cellular immune responses by Tylophora indica in
experimental models, Phytomedicine, 8, 348, 2001.
96. Shinde, U.A., Kulkarni, K.R., Phadke,
A.S., et al., Mast cell stabilizing and lipooxygenase
activity of Cedrus deodara Loud. wood oil, Indian J. Exp. Biol., 37, 258, 1999.
97. Ammon, H.P.T., Mack, T., Singh, G.B., et
al., Inhibition of LT B4-formation in rat peritoneal
neutrophils by an ethanolic extract of the
gun resin extract of Boswellia serrata, Planta Med.,
57, 203, 1999.
98. Paulino, N., Cechinel-Filho, V., Yunes,
R.A., et al., The relaxant effect of extract of Phyllanthus
urinaria in the guinea pig isolated trachea:
evidence for involvement of ATP-sensitive potassium
channels, J. Pharm. Pharmacol., 48, 1158, 1996.
99. Kim, Y.C., Lee, E.H., Lee, Y.M., et al.,
Effect of the aqueous extract of Aquilaria agallocha stems
on the immediate hypersensitivity reactions, J. Ethnopharmacol., 58, 31, 1997.
100. Kumar, V.L., Basu, N., Anti-inflammatory
activity of the latex of Calotropis procera, J. Ethnopharmacol.,
44, 123, 1994.
101. al-Zuhair, H., el-Sayeh, B., Ameen,
H.A., et al., Pharmacological studies of cardamom oil in
animals. Pharmacol. Res., 34, 79, 1996.
102. Mediratta, P.K., Sharma, K.K., and
Singh, S., Evaluation of immunomodulatory potential of
Ocimum sanctum seed oil and its possible
mechanism of action, J.
Ethnopharmacol., 80, 15,
2002.
103. Kelm, M.A., Nair, M.G., Strasburg, G.M.,
et al., Antioxidant and cyclooxygenase inhibitory
phenolic compounds from Ocimum sanctum Linn.,
Phytomedicine, 7, 7, 2000.
104. Singh, S. and Majumdar, D.K., Effect of
Ocimum sanctum fixed oil on vascular permeability
and leucocytes migration, Indian J. Exp. Biol., 37, 1136, 1999.
105. Mujumdar, A.M., Dhuley, J.N., Deshmukh,
V.K., et al., Anti-inflammatory activity of piperine,
Jpn. J. Med. Sci. Biol., 43, 95, 1990.
106. Doshi, V.B., Shetye, M., Mahashur, A.A.,
et al., Picrorrhiza kurroa in bronchial asthma, J.
Postgrad. Med., 29, 89, 1983.
107. Govindan, S., Vishwanathan, S.,
Vijayashekaran, et al., A pilot study on the efficacy of Solanum
xanthocarpum and Solanum trilobatum in
bronchial asthma, J.
Ethnopharmacol., 66, 205,
1999.
108. Jain, J.P., A clinical trial of
Kantakari (Solanum xanthocarpum) in cases of Tamak Swasa (some
respiratory diseases), J. Res. Ayurveda Siddha, 1, 447, 1980.
109. Gupta, P.P., Dubey, S.D., Mishra, J.K.,
et al., A comparative study on brihati and kantakari in
svasa and kasa, J. Res. Ayurveda Siddha, 20, 191, 1999.
110. Shivpuri, D.N., Menon, M.P.S., and
Prakash, D., Preliminary studies an Tylophora indica in
the treatment of asthma and allergic
rhinitis, J.
Assoc. Physicians India, 16,
9, 1968.
111. Shivpuri, D.N., Singal, S.C., and
Parkash, D., Treatment of asthma with an alcoholic extract
of Tylophora indica: a cross over, double
blind study, Ann.
Allergy, 30, 407,
1972.
112. Mathew, K.K. and Shivpuri, D.N.,
Treatment of asthma with alkaloids of Tylophora indica: a
double blind study, Aspects Allergy Appl. Immunol., 7, 166, 1974.
113. Thiruvengadam, K.V., Harnath, K.,
Sudarsan, S., et al., Tylophora indica in bronchial asthma,
J. Indian Med. Assoc., 71, 172, 1978.
114. Gupta, S., George, P., Gupta, V., et
al., Tylophora indica in bronchial asthma: a double blind
study, Indian J. Med. Res., 69, 981, 1979.
115. Gupta, I., Gupta, V., Parihar, A., et
al., Effects of Boswellia serrata gum resin in patients with
bronchial asthma: results of a double blind,
placebo-controlled, 6 week clinical study, Eur. J.
Med. Res., 3, 511, 1998.
116. Iyenger, M.A., Jambaiah, K.M., Kamath,
M.S., et al., Studies on an anti-asthmatic kada — a
proprietary herbal combination. I. Clinical
study, Indian Drugs, 31, 183, 1994.
117. Shankar, A., Parsai, M.R., Naqvi,
S.M.A., et al., A clinical trial of Bharangi in cases of Tamaka
Swasa (bronchial asthma), J. Res. Ayurveda Siddha, 1, 470, 1980.
118. Sharma, G.D., Upadhyay, B.N., and
Tripathi, S.N., A clinical trial of Euphorbia prostrata and
Euphorbia thymifolia in the treatment of
bronchial asthma, J. Res.
Ayurveda Siddha, 3, 109,
1982.
119. Swamy, G.K., Bhattathiri, P.P.N., Rao,
P.V., et al., Clinical evaluation of Sirisa Twak Kvatha in
the management of Tamaka Shwasa (bronchial
asthma), J. Res.
Ayurveda Siddha, 18, 21,
1997.
120. Trivedi, V.P., Nesamany, S., and Sharma,
V.K., A clinical study of the anti-tussive and antiasthmatic
effects of Vibhitakphal churna (Terminalia
belerica) in the cases of Kasa-swasa, J.
Res. Ayurveda Siddha, 3, 1, 1982.
Om Tat Sat
(Continued...)
(My
humble salutations to H H Maharshi ji, Brahmasri
Sreeman Lakshmi Chandra Mishra ji and other eminent medical scholars and
doctors for the collection)
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