Involvement of nitric oxide in 5-HT 3 receptor agonist-induced fluid accumulation in jejunum and colon of anesthetized rats
Objectives : The aim of the present study was to investigate the involvement of nitric oxide in 5-HT3 receptor agonist-induced fluid accumulation in jejunum and colon of anesthetized rats. Materials and Methods : Fluid movement in jejunum and colon were determined simultaneously in the same rat, by...
Saved in:
Published in | Indian journal of pharmacology Vol. 41; no. 5; p. 221 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Pondicherry
Medknow Publications and Media Pvt. Ltd
01.09.2009
Medknow Publications & Media Pvt. Ltd |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Objectives : The aim of the present study was to investigate the involvement of nitric oxide in 5-HT3 receptor agonist-induced fluid accumulation in jejunum and colon of anesthetized rats. Materials and Methods : Fluid movement in jejunum and colon were determined simultaneously in the same rat, by modifying the Beubler method. Nv-nitro-L-arginine (L-NNA, 20 mg/kg, s.c) alone and in combination with L-arginine (L-Arg, 150 mg/kg s.c) or D-arginine (D-Arg, 150 mg/kg, s.c) were administered 30 min before administration of 1-PBG (18.5 μg/kg, i.v). Results : Intravenous administration of 1-phenylbiguanide (1-PBG) induced a net secretion of fluid in both jejunum and colon. 1-PBG had a more prominent secretory effect in the colon, causing a three-fold increase in volume of fluid secreted/g of colon than in the jejunum. Pretreatment with (L-NNA) prevented the 1-PBG-induced fluid accumulation in both jejunum and colon. The inhibitory effect of L-NNA on 1-PBG-induced fluid accumulation was reversed by L-Arg but not by D-Arg. Conclusion : These results provide evidence that nitric oxide plays an important role in 5-HT3 receptor agonist-induced fluid accumulation in jejunum and colon of anesthetized rats. |
---|---|
ISSN: | 0253-7613 1998-3751 |
DOI: | 10.4103/0253-7613.58511 |