In vitro And In vivo Activities of Stem Bark of Methanolic Extract of...

[Full title: In vitro And In vivo Activities of Stem Bark of Methanolic Extract of Ailanthus Excelsa Roxb. in the Management of Asthma]

Life International Journal of Pharmacology ISSN 1811-7775 Life science alert ansinet Asian Network for Scientific Information

International Journal of Pharmacology 6 (3): 284-289, 2010 ISSN 1811-7775 2010 Asian Network for Scientific Information In vitro and in vivo Activities of Stem Bark of Methanolic Extract of Ailanthus Excelsa Roxb. in the Management of Asthma Dinesh Kumar, S.S. Bhujbal, P.S. Patil and P. V. Buge 'Rayat Institute of Pharmacy, Railmajra, S.B.S. Nagar, Punjab, India Department of Pharmacognosy, Padamshree. Dr. D. Y. Patil Institute of Pharmaceutical Science and Research, Pimpri, Pune-411018, India Abstract: The aim of study was in vitro and in vivo activities of stem bark of methanolic extract of Ailanthus excelsa Roxb. in the management of asthma. Ailanthus excelsa Roxb. used in Indian system of medicine in the treatment of asthma, bronchotitis, cold colic pain etc. Methanolic extract of stem bark of Ailanthus excelsa was evaluated using in vitro- goat tracheal chain preparation model and in vivo- milk induced leucocytosis, milk induced eosinophilia and clonidine induced catalepsy in mice models. Dose response studies of methanolic extract were conducted at 30 μg mL. ' in vitro and 100, 200, 400 mg kg ´p.o. in vivo models. Treatment with methanolic extract of stem bark of Ailanthus excelsa at 30 μg mL in vitro and 100, 200, 4100 mg kg p.o. in vivo showed significant reduction in signs and severity of symptoms (*p<0.05, **p<0.01, ***p<0.001). The findings from various studies reveal that the antihistamine activity of methanolic extract of stem bark of Ailanthus excelsa may be due to the reduction in histamine induced contraction in goat tracheal chain preparation model and mast cell stabilizing potential. Inhibition of release of inflammatory mediators by decreasing total leucocytes and eosinophiles count, potentiate the antiasthmatic activity. L Key words: Antiasthmatic activity, Ailanthus excelsa roxb, clonidine induced catalepsy INTRODUCTION Asthma is a chronic inflammatory disease that affects about 300 million people worldwide, a total that is expected to rise to about 400 million over the next. 15-20 years. Most asthmatic individuals respond well to the currently available treatments of inhaled corticosteroids and B-adrenergic agonists; however. 5-10% has severe disease that responds poorly. Allergic asthma is a chronic airway disease with characteristic features like airway inflammation, epithelial damage. increased production of reactive oxygen species and airway hyper responsiveness to a variety of specific und nonspecific stimuli (Henricks and Nijkamp, 2001; Tobin, 2001). The supposed initial step in the allergic response is the cross linking of antigen-specific, mast cell-bound immunoglobulin (Ig) E, which upon re-exposure to allergen, leads to mast cell degranulation and the consequent release of inflammatory mediators, such as histamine and leukotrienes (Krishnaswamy et al., 2001). These mediators cause airway obstruction, known as the early asthmatic response. Moreover, mast cells release a variety of chemotaxins and cytokines, which promote infiltration and activation of inflammatory cells, like macrophages and eosinophils, into the lungs (Krishnaswamy et al., 2001). These cells, logether with their products, play key roles in the development and maintenance of the characteristic features of asthma. (Busse and Leranske, 2001, Sacila, 1999). Allergy is one of the common diseases that affect mankind with diverse manifestations. The prevalence of allergy and asthma has risen in the recent years despite an improvement in the general health of the population (Gopumadhavan et al., 2005). Ailanthus is a deciduous tree belonging to the family Simarubaceae and widely distributed in Asia and North Australia. Commonly it is known as a plant of Heaven. Tree of heaven is fast. growing extensively cultivated in many parts of India towards the vicinity of villages. The tree is indigenous to Southern and Central India and distributed in Western Peninsula, Rajasthan, Bihar, Orissa, Bundelkhand, through Madhya Pradesh, Broach and Panchamal district. of Gujarat, in dry deciduous forests of Maharastra, scrace in Deccan and Karnataka, N. Circars, forest of Tamilnadu in India. It is often planted along the roads. It is exotically found in Sudan. The plant is known for its high economical and commercial importance (Anonymous 1985; Database, 2000). Biologically active compounds Corresponding Author: Dinesh Kumar, Department of Pharmacognosy, Rayat Institute of Pharmacy, Railmajra, S.B.S. Nagar, Punjab, India Tel: +91 9501456827/+91 9975813867 Fax: +912027420261 284

Int. J. Pharmacol., 6 (3): 284-289, 2010 from natural sources are of interest as possible new drugs for infectious diseases. The bark of this plant is used as an anthelminthic, expectorant, astuna (Lavhale and Mishra, 2007), antispasmodic (Kirtikar and Basu, 1933) and antipyretic (Suresh and Dhansekran, 1990). Indigenous preparations from A. excelsa were shown to be effective in the realment of WOTTH infections (Sharma and Ojha, 1992) Ailanthus excelsa is a rich source of different chemical compounds with a variety of potential biological activities (Kapoor et al., 1971). The present study was designed to test the in vitro and in vivo asthmatic activity of methanolic extract of stem bark of 1. excelsa. MATERIALS AND METHODS Plant material: Stem barks of Ailanthus excelsa Roxb were collected in Aug. 2008 from local area of Pimpri, pure-18 (India) and identified by the Regional research institute of Ayurveda Kothrude, Pume (India). A voucher specimen - 899 was authenticated. Stem barks were dried. powdered pass through 40 mesh sieve. The powdered material was extracted with methanol using continuous hot extraction method (Soxhlet method) (Trease and Evans, 2002). The extract obtained was dried, yielding a dark brown colored powdery mass (5%). Animal: Isolated adult goat tracheal tissue, Albino mice (Wistar Strain) of either sex weighing 20-25 g, respectively were used for studies. Isolated adult goat trachea tissue was obtained immediately after slaughter of the animal. Pieces of the trachea were collected in the ice cold oxygenated Krebs solution. The albino mice were obtained from animal house of National Toxicological Centre (NTC), Pune. They were housed in polypropylene cages with standard pellet chow and water ad libitum. In all experimental sets, 5 mice were used for each treatment. Acute toxicity studies: Mice were selected for this study. They were divided into eight groups each containing 6 animals. Methanolic extract of A. excelsa was administered orally in varying doses (0.50, 0.75, 1.00, 1.25. 1.50, 1.75, 2.00 and 2.50 g kg¯) to these animals. They were continuously observed for 2 h to detect changes in the autonomic or behavioral responses like alertness, spontaneous activity, irritability, urination, etc. Any mortality during experimentation and the following 7 days was also recorded. A group of animals treated with vehicle (distilled water) was served as control. Based on the results of preliminary toxicity testing the doses of 100, 200 and 400 mg kg po. were chosen for further experiments (Kumar et al., 2010). Antiasthmatic activity In vitro method Effect of test drug on isolated goat trachea chain preparation (Kulshrestha et al., 1983): Isolated adult Goat tracheal tissue was obtained immediately after slaughter of the animals. Trachea was cut into individual rings and tied together in series to form a chain. Trachea was suspended in bath of Kreb's solution of the composition: NaCl 6.9, KCI 0.35, CaCl, 0.28, MgSO40.28. NaHCO, 2.1, KH,PO, 0.16 and Glucose 2.0 g L, which was continuously aerated and maintained at 37=0.5°C. One end of the tracheal chain was altached to an S-shaped aerator tube and other attached to an isotonic frontal writing lever to smoked drum (magnification 10-12 folds). Tissue was allowed to equilibrate for 45 min under a load of 400 mg (NagChaudhari and Lahiri, 1974). A dose response curve for histamine was taken in variant. molar concentrations, by maintaining 15 min time cycle. After obtaining a dose response curve of histamine on trachea, the Ailanthus excelsa extracts were added to the respective reservoir and same doses of histamine were repeated. Graph of percentage of maximum contractile response on ordinate and negative logarithm of molar concentration of histamine on abscissa were plotted to record dose response curve of histamine, in absence and in presence Ailanthus excelsa extracts. In vivo method Effect of test drug on leukocytosis (Brekhman and Dardimov, 1969; Vadnere et al., 2007): Mice were divided into five groups, five animals in each group. Animals belonging to group-l received Distilled Water (DW) 10 ml kg ', (p.o.). Animals belonging to group IT. III, IV and V received boiled and cooled milk injection in dose of 4 ml kg, (s.c.). Animals belonging to groups III, IV and V received test extract of Ailanthus excelsa Roxb. in dose 100, 200 and 400 mg kg, p.o. respectively, 1 h before milk injection. Blood samples were collected from each mouse from the retro orbital plexus, under light ether anesthesia. Total leukocyte count was done in each group before drug administration and 24 h after milk injection. Difference in total leukocyte count before and 24 h after drug administration was calculated. Effect of test drug on cosinophilia (Brekhman and Daradimov, 1969; Vadnere et al., 2007): Mice were divided into five groups, five animals in each group. Animals belonging to group-I received distilled water (DW) 10 mL ke, (p.o.). Animals belonging to group II, III IV and V received boiled and cooled milk injection in dose of 1 mL kg, (s.c.). Animals belonging to groups III, TV and V received test. extract of Ailanthus excelsa Roxb. 285

Int. J. Pharmacol., 6 (3): 284-289, 2010 in dose 100, 200 and 400 mg kg, p.o. respectively, 1 h before milk injection. Blood samples were collected from each mouse from the retro orbital plexus, tider light, ether anesthesia. Total Eosinophilia count was done in each group before drug administration and 24 h after milk injection. Difference in total eosinophilia count before and 24 h after drug administration was calculated. Effect of test drug on Clonidine-induced Catalepsy (Ferre et al., 1990; Taur et al., 2007): Bar test was used to surly the effect of test drug extracts on Clonidine induced catalepsy. Mice were divided into five groups, five animals in each group. Animals belonging to group T served as control and were administered the vehicle (10 mL kg, po.). Animals belonging to group II received standard drug Chlorpheniramine maleate (10 mg kg-1, ip.). Animals belonging to groups III, IV and V received three doses 100, 200 and 400 mg kg p.o., respectively of Roxb. methanolic extract. The forepaws of mice were placed on a horizontal bar (1 cm in diameter, 3 cm above the table) and the time required to remove the paws from bar was noted for each animal. All the groups received Clonidine (1 mg kg, s.c.), 1 h after the test drug administration and the duration of catalepsy were measured at 15, 30, 60, 90, 120, 150 and 180 min. 1Statistical analysis: All values were expressed as Mean±SEM and data were analyzed by ANOVAs followed by denmest. RESULTS Effect of methanolic extract of Ailanthus excelsa Roxb. on histamine induced contraction of isolated goat tracheal chain preparation: In the present study, it was observed that Ailanthus excelsa inhibits the contraction produced by histamine in these tissue preparations. Histamine (10 μg mL) was taken in different dose level and DRC was plotted in absence and in presence of Ailanthus excelsa extrael. Study showed that. Ailanthus excelsa extract inhibits significantly (*p<0.05, **p<0.01, ***p<0.001) percentage contraction al concentration 30 μg mL in goat tracheal chain preparation (Table 1). Effect of Ailanthus excelsa Roxb. stem barks methanolic extract (AESM) on Milk-Induced Leucocytosis in mice: Subcutaneous injection of milk at dose of 1 mL kg¹ produced a significant. (***p<0.001) increase in the leucocytes count after 24 h of its administration. In the groups of mice pretreated with methanolic extract of Ailanthus excelsa Roxb. at. dose (100, 200 and Table 1: Effect of Alianthus excelsa Raxh. ABSM (30 µg/mL. ') on histamine induced contraction of isolated goat tracheal chain preparation -Ve Log molar Maximum contraction (%) Dose (10 µg mL) concen of Histanine sonsen. Histamine 0.1 0.2 0.4 0.8 1.6 3.2 (6.1 Control AESM (30 ug mL¯¹) 7.08 21.85±1.232 12.58+0.7491 6.75) 36.42+1.833 17.88+0.922* 6.48 47.02+1.797 22.51+0.8819* 6.18 61.59±1.945 35.09±0.9804" 5.88 84.11+3.156 42.38±1.563" 5.58 90.0712.525 15.7011.088** 5.23 1002411 51.3011.200** n = 5, Values are in Mean LSTM. Control DRC of Ilistamine in absence of Ailanthus excelsa Roxb. extract. AESM DRC of Histamine in presence of Ailanthus excelsa Roxb extract. (30 μg mL. Statistical analysis done by using Student's t-test. *p<0.05, **p<0.01, ***p<0.001 significantly different from control Table 2: Effect of Ailanthus excelsa Roxb. stem barks methanolic extract (ATSM) on Milk-Induced Leucocytosis in mice Dose Control (Vehicle (10 mL kg. p.o.) Intox. (milk 1 mL kg ) ABSM100 AESM200 AESM400 Difference in no. of leucocytes (cu/mm) (Mean STM) 80±12.247 1510 507.51*** 2990-186.16* 2110=364.49** 1580 53.852** Vehicle (10 mL. kg 11 = 5, values are expressed in meantSFM. Control p.a.). Intex milk 4 mL kg. AESM100 Ailanthus excelsa Roxb. Stern bark methanolic extract (100 mg kg, p.o.). AESM200 Ailanthus excelsa Roxb. Stem bark methanolic extract (200 mg kg-1, p.o). AESM400= Ailanthus excelsa Roxb. Stem bark methanolic extract ((400 mg kg, p.o.). ***p<0.001, Intox. group compared with control group using student't, test. and*p<0.05, **p<0.01, AFSM compared to intox. Group using statistical analysis done by ANOVA followed by Dunet's test 400 mg kg, p.o.), there was significant (*p<0.05, **p<0.01) inhibition of milk-induced Leucocytosis (Table 2). Effect of Ailanthus excelsa Roxb. stem barks methanolic extract (AESM) on Milk-Induced Eosinophilia in mice: Injection of Milk (4 mL kg¯', s.c.) produced a significant (***p<0.001) increase in the total eosinophil count. In the groups pretreated with methanolic extract of Ailanthus excelsa Roxb. at dose (100, 200 and 400 mg kg, p.o.), there was significant. (**p<0.01) inhibition of milk-induced eosinophilia and the eosinophil count was 92.619.605, 89±7.969 and 64.8±6.771 cu mm, respectively (Table 3). Effect of Ailanthus excelsa Roxb. AESM on Clonidine induced catalepsy in mice: Clonidine (1 mg kg, s.c.) produced catalepsy in mice, which remained for 2 h. The vehicle treated group showed maximum duration of catalepsy (80.2±3.813 sec) at 120 min after the administration clonidine. There was significant inhibition (*p<0.05, **p<0.01) of clonidine induced catalepsy in the animals pretreated with Ailanthus excelsa Roxb. AESM extract (100, 200 and 400 mg kg 'po) and the duration of 286

Int. J. Pharmacol., 6 (3): 284-289, 2010 Table 3: Effect of Alianthus exceira Roxb. stem barks methanolic extract. (ATSM) on Milk-Induced Rosinophilia in mice Dose Control Intox. (milk 4 mL kg) AESM100 AESM200 AESM400 Difference in no. of eosinophils (cu/mm) (Mean SDM) 21.8-2.973 150.4±8.744*** 92.6±2.605** 89.0±7.969*** 64.8±6.771** 11 = 5, Values are expressed in mean±SEM Control Vehicle (10 mL kg, p.o.). Intox. milk 1 mL kg AESM100 = Ailanthus excelsa Roxb. Stem bark methanolic extract (100 mg kg, p.o.). AESM200= Ailanthus excelsa Roxb. Stem bark methanolic extract (200 mg kg, p.o). AESM100= Ailanthus excelsa Roxb. Stem bark methanolic extract (100 mg kg¯', p.o.) ***p<0.001, Intoxx group compared with control group using student't, test and **p<0.01, AESM compared to intooc Group using Statistical analysis done by ANOVA followed by Dunnet's test Table 4: Effect of Ailanthus excelsa Roxb. (AESM) on Clonidine-induced catalepsy in mice Duration of catalepsy (Sec) at Mean±SEM 15 30 60 90 120 150 180 Group Control Std. 23.211.655 41.6-2.112 49-1.871 13.211.281** 17.6-0.9274 AESM 100 20.411.364 36.2-2.082 25.211.281**** 37.212267 -(min)- 55.241.356 3211.949 48411.536" 80.213.813 3.5.81.9340 50.811.934" 8016618 616.612.768 56.211.855 20.8-2.577 59.811.9340 56.4-3.572 ABSM 200 1911.304 36.2-1.655 ABSM 400 17.810.8602" 22.8 1.393 39.213.926" 30.612.619 38411.327 34.81.355 56.413.945" 505.422 43.6-2.482 42211.744 41.62.112 38.4-1.327 N = 5, Control = Distilled water (10 mL kg, p.o.). Std. - Chlorpheniraminc malcate (10 mg kg, i.p.). AESM 100 = Ailanthus excelsa Roxb. Stem bark methanolic extract (100 mg kg, p.o.). AESM 200 Ailanthus excelsa Roxb. Stem bark methanolic extract (200 mg kg¹. p.o.). AESM 400 = Ailanthus excelsa Roxb. Stom bark methanolic extract (400 mg kg-1, p.o.). Statistical analysis donc by ANOVA followed by Dunnett's test. "p<0.05, **p<0.01, compared to control group catalepsy was found to be 60.8±1.934, 56.4±3.945 and 42.211.744 sec, respectively al 120 min after the administration clonidine. Chlorpheniramine maleate (10 mg kg, ip) significantly inhibited (**p<0.01) clonidine induced catalepsy in mice at 120 min alter the administration clonidine (Table 4). DISCUSSION Histamine contracts the tracheobronchial muscle of guinea pig, goat, horse, dog and man. Goat tracheal chain. is easier to handle and to prepare, it is also much more sensitive than guinea pig tracheal chain (Bhujbal et al.. 2009). Therefore, the dose relative contractile responses of clifferent agonists like Ach, histamine. 5-hydroxytryptamine and bradykinin can be observed in isolated goat trachea. In the present study, the isolated goat tracheal chain preparation; there is right side shift of Dose Response Curve (DRC) of histamine in the presence of Ailanthus excelsu Roxb. ex Tacl indicating antihistaminic which help to reduce the histamine which is a mediator for asthma (Taur et al., 2007). Ayurveda provides a number of herbs for the treatment of asthma and herbal formulations used for the treatment of asthma include some antistress (nervine support) herbs to enable adoption to stress, since, excessive stress or nervous debility may aggravate the symptoms of asthma. After parenteral administration of milk there is increase in TLC and this stressful condition can be normalized by administration of an antistress or adaptogenic drug (Brekhman and Darcimov, 1969). Furthermore, leukocytes recruited during asthmatic inflammation release the inflammatory mediators like cytokines, histamine and major basic protein and promote the ongoing inflammation. This model was used to evaluate the protective effect of Ailanthus excelsa Roxb. against milkinduced leukocytosis. Eosinophilia is an abnormal increase in peripheral cosinophil count to more than 4% of total leukocytes. In the late phase, especially in the development of allergic asthma, eosinophils play role as an inflammatory cell. Eosinophil secretes mediators such as Eosinophil Cationic Protein (ECP), eosinophil derived neurotoxin (EDNT), Granulocyte Macrophage Colony Stimulating Factor (GM-CSF), Tumor Necrosis Factor (TNF) and Prostaglandin (PG), which results in epithelial shedding, bronchoconstriction and promotion of inflammation in respiratory tract often allergic (Osama and Joshi, 1984). Eosinophilia is associated with respiratory disorder and nature together with pulmonary infiltrates that are detectable on chest films (Chright and Chua, 1989). Most of the literatures do not include a diagnostic evaluation and precise practical clinical approach to eosinophilia (Karnick, 1995) performed clinical studies and assessed the role of eosinophil in asthmatic response. T. was also demonstrated that parental administration of milk produces a marked and significant increase in the eosinophils count after 24 h of its administration (Bhargava and Singh, 1981). The milk induced leucocytosis and cosinophilia. models helps to evaluate the stress induced asthma and Ailanthus excelsa helps to reduce the stressed astma. Clonidine, a c₂ adrenoreceptor agonist induces dose dependent catalepsy in mice, which 287

Int. J. Pharmacol., 6 (3): 284-289, 2010 is inhibited by histamine (H) receptor antagonists but not by II, receptor antagonist. It is known that clonidine releases histamine from mast cells. Brain histamine does play a definite role in the production of the extra pyramidal motor it has been suggested that the cataleptic effect of clonidine in the mouse be mediated by histamine (via II, receptors) which is released from brain mast cells in response to stimulation of adrenoreceptors by clonidine (Wardlaw et al., 2002). The extract also significantly inhibited the clonidine induced catalepsy. The inhibition of clonidine induced catalepsy by Ailanthus excelsa Roxb. may be due to the potential to antagonize II, receptor or inhibition of mast cell degranulation induced by clonidine. can Thus, we know that asthma has several types and it can be concluded from the results obtained in the present investigation that methanolic extract of stem bark of Ailanthus excelsa Roxb. possess significant anti-asthmatic activity and be attributed to antihistaminic (H.-antagonist), antistress activity, suggestive of its potential in prophylaxis and management of asthma. Hence further detailed study needs to be conducted to evaluate the phytoconstituent responsible to produce above result and their clinical efficacy in the treatment of asthmatic patients. ACKNOWLEDGMENTS We would like to acknowledge that this research was supported by Dr. D. Y. Patil IPSR, Pimpri, Pune-18 (India) by providing the lab facility. We would also like to thank Dr. Rajesh Dabour for authentication the plant sample in R.R. I. Pune (India). REFERENCES Anonymous, 1985. The Wealth of India (Raw Material). Vol. 1A, Publication and Information Directorate, CSIR New Delhi. Bhargava, K.P. and N. Singh, 1981. Antistress activity of Ocimum sanctum (Linn). Indian J. Med. Res., 73: 443-451 Bhujbal, S.S., D. Kumar, R.S. Deoda, T.K. Deore and M.J. Patil, 2009. Antiasthmatic activity of roots of Hemidesmus indicus R. Br. Pharmacologyonline. 1: 209-216. Brckhman, 1.1. and I. V. Dardimov, 1969. New substances of plant origin which increase non-specific resistance. Annu. Rev. Pharmacol., 9: 419-430. Busse, W.W. and R.F. Lemanske, 2001. Asthma. N. Engl. J. Med., 344: 350-362. Database, 2000. Medicinal Plants Used in Ayurveda. Central Council for Research in Ayurveda and Siddha. New Dhli, India, pp: 50-59. Ehright, T. and S. Chua, 1989. Pulmonary eosinophilic syndromes. Ann. Allergy, 62: 277-283. Ferre, S., T. Guix, G. Part, F. Jane and M. Casas, 1990. Is experimental catalepsy properly measured? Pharmeol. Biochem. Behav., 35: 753-757. Gopumadhavan, S., M. Rafiq, M.V. Venkataranganna and S.K. Mitra, 2005. Antihistaminic and antianaphylactic activity of IIK-07, a herbal formulation. Indian J. Pharmacol., 37: 300-300. Ilenricks, P.A. and F.P. Nijkamp, 2001. Reactive oxygen species as mediators in asthma. Pulm. Pharmacol. Ther., 14: 409-420. Kapoor, S.K., P.I. Ahmad and A. Zaman, 1971. Chemical constituents of Ailanthus excelsa. Phytochemistry, 10: 3333-3335. Kamnick, C.R., 1995. Clinical observation on the effect of Solanum khasianum Linn on tropical pulmonary eosinophilia. Aryacaiidyan, 8: 185-187. Kiitikar, K.R. and B.D. Basu, 1933. Indian Medicinal Plants. 2nd Edn, Lalit Mohan Basu, Allahabad, India. pp: 179-180. Krishnaswamy, G., J. Kelley, D. Johnson, G. Youngberg and W. Stone et al. 2001. The human mast cell: Functions in physiology and disease. Front. Biosci., 6: D1109-D1127. Kulshrestha, S.S., S. Misra, A.L. Sharma, P. Sharma and D. Singhal, 1985. Response of the goal trachea to some autonomic drugs. Indian J. Pharmacol., 15: 107-109. Kumar, D., S.S. Bhujbal, R.S. Deoda and S.C. Mudgade. 2010. in vitro and in vivo Antiasthmatic studies of Ailanthus excelsa Roxb. on Guinea Pigs. J. Sci. Res., 2: 196-202. Lavhale, M.S. and S.H. Mishra, 2007. Nutritional and therapeutic potential of Ailanthus excelsa: A review. Pharmacognosy Rev., 1: 105-113. NagChaudhari, A.K. and S.C. Lahiri, 1974. Use of Goat. trachea isolated tracheal chain preparation. Indian J. Pharmacol., 6: 149-151. Osama, N.O. and K.R. Joshi, 1981. Immunology: Immunology of Respiratory Disease. Agro Botanical Publishers, Bikaner, pp: 321-329. Saetta, M., 1999. Airway inflammation in chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med., 160: 817-820. Sharma, B.P. and D. Ojha, 1992. The management of Gandupoda krimi (Ascaris lumbricoides) with indigenous drugs. Aryavaidyan, 5: 170-170. 288

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Ailanthus excelsa, Tree of heaven, Animal, Vehicle, Allergy, Mortality, Asthma, Nervous system, Statistical analysis, Prophylaxis, Clinical efficacy, Plant material, Acute Toxicity Studies, Reactive oxygen species, In vitro, Antistress activity, Eosinophil Count, Airway inflammation, Airway obstruction, Eosinophil, Albino mice, Catalepsy, Voucher specimen, Methanolic extract, Total leukocyte count, Histamine, Histamine-induced contraction, Biological activities, In vivo, Airway hyper responsiveness, Antihistaminic activity, Antistress herb, Eosinophilia, Chronic inflammatory disease, In vivo method, In vitro method, Airway hyperresponsiveness, Leukocytosis, Dose response curve, Antiallergic Activity, Antipyretic, Deciduous tree, Stem Bark, Inflammatory disease, Expectorant, Chlorpheniramine maleate, Biologically active compound, Anti-asthmatic activity, Mast cell degranulation, Antispasmodic, Allergic asthma, Milk induced leukocytosis, Antiasthmatic activity, Soxhlet method, H2 receptor antagonist, Potential biological activities, Stem bark extract, Milk induced eosinophilia, Milk induced leucocytosis, Phytoconstituent, Behavioral response, Tumor necrosis factor (TNF), In-vivo activities, Clonidine induced catalepsy, H1 Receptor Antagonist, Retro-orbital plexus, Epithelial damage, Adaptogenic drug, Mast cell, Inflammatory mediator, Inhaled corticosteroid, Kreb's solution, Macrophage, Antihistaminic, Cytokine, In vitro activities, H1 receptor, Inflammatory cell, Stressful condition, Clonidine, Autonomic response, Pulmonary infiltrates, Asthmatic inflammation, Leukotrienes, Leukocyte count, Leukocyte, Krebs solution, Immunoglobulin (Ig) E, Brain mast cells.