RESEARCH ARTICLE |
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Year : 2012 | Volume
: 44
| Issue : 2 | Page : 197-203 |
Molecular docking and ex vivo pharmacological evaluation of constituents of the leaves of Cleistanthus collinus (Roxb.) (Euphorbiaceae)
Subramani Parasuraman1, Ramasamy Raveendran1, Balakrishnan Vijayakumar2, Devadasan Velmurugan3, Subramani Balamurugan4
1 Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry, India 2 Centre of Advanced Study in Crystallography and Biophysics, University of Madras, Maraimalai (Guindy) Campus, India 3 Centre of Advanced Study in Crystallography and Biophysics and Bioinformatics Infrastructure Facility (BIF), University of Madras, Maraimalai (Guindy) Campus, India 4 College of Pharmacy, Madras Medical College, Chennai, India
Correspondence Address:
Subramani Parasuraman Department of Pharmacology, Jawaharlal Institute of Postgraduate Medical Education and Research, Pondicherry India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/0253-7613.93848
Objective: To investigate the involvement of alpha adrenergic receptors in hypotension induced by cleistanthin A and cleistanthin B.
Materials and Methods: Cleistanthins A and B were isolated from the leaves of Cleistanthus collinus using a column chromatographic method and purified. Structures were confirmed by spectroscopic analysis. The compounds were prepared for molecular docking studies using Ligprep 2.3 module and Induced Fit Docking was carried out against α-1 adrenergic receptors using Glide. The ex vivo experiments were carried out on male Wistar rats. Under anaesthesia, the femoral vein and carotid artery were cannulated for drug administration and for monitoring the blood pressure, respectively. The effect of epinephrine, norepinephrine, acetylcholine, histamine and dopamine were recorded before and after the administration of cleistanthin A or cleistanthin B. The molecular docking studies showed favorable molecular interactions, glide score, energy and emodel.
Result: Cleistanthins A and B per se reduced the mean blood pressure and the effect was dose dependent. Both the compounds reduced the effect of epinephrine, norepinephrine and α-1 receptor activity of dopamine. Cleistanthin B significantly increased the duration of action of acetylcholine on mean blood pressure.
Conclusion: The molecular docking and ex vivo studies conclude that cleistanthin A and cleistanthin B have significant α-1 adrenergic receptor antagonist effect on the peripheral vascular system.
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