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Effects of inhibitors of hydrogen sulphide synthesis on rat colonic motility
Author(s) -
Gil V,
Gallego D,
Jiménez M
Publication year - 2011
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/j.1476-5381.2011.01431.x
Subject(s) - motility , aminooxyacetic acid , cystathionine beta synthase , chemistry , tetrodotoxin , nitric oxide , nitric oxide synthase , endogeny , interstitial cell of cajal , hyperpolarization (physics) , biochemistry , biophysics , endocrinology , biology , enzyme , cysteine , microbiology and biotechnology , smooth muscle , stereochemistry , nuclear magnetic resonance spectroscopy , organic chemistry
BACKGROUND AND PURPOSE The role of hydrogen sulphide (H 2 S) as a putative endogenous signalling molecule in the gastrointestinal tract has not yet been established. We investigated the effect of D,L‐propargylglycine (PAG), an inhibitor of cystathionine γ‐lyase (CSE), amino‐oxyacetic acid (AOAA) and hydroxylamine (HA), inhibitors of cystathionine β‐synthase (CBS) on rat colonic motility. EXPERIMENTAL APPROACH Immunohistochemistry, H 2 S production, microelectrode and organ bath recordings were performed on rat colonic samples without mucosa and submucosa to investigate the role of endogenous H 2 S in motility. KEY RESULTS CSE and CBS were immunolocalized in the colon. H 2 S was endogenously produced (15.6 ± 0.7 nmol·min −1 ·g −1 tissue) and its production was strongly inhibited by PAG (2 mM) and AOAA (2 mM). PAG (2 mM) caused smooth muscle depolarization and increased spontaneous motility. The effect was still recorded after incubation with tetrodotoxin (TTX, 1 µM) or N ω ‐nitro‐L‐arginine (L‐NNA, 1 mM). AOAA (2 mM) caused a transient (10 min) increase in motility. In contrast, HA (10 µM) caused a ‘nitric oxide‐like effect’, smooth muscle hyperpolarization and relaxation, which were antagonized by 1H‐[1,2,4]oxadiazolo[4,3‐α]quinoxalin‐1‐one (ODQ, 10 µM). Neither spontaneous nor induced inhibitory junction potentials were modified by AOAA or PAG. CONCLUSIONS AND IMPLICATIONS We demonstrated that H 2 S is endogenously produced in the rat colon. PAG and AOAA effectively blocked H 2 S production. Our data suggest that enzymatic production of H 2 S regulates colonic motility and therefore H 2 S might be a third gaseous inhibitory signalling molecule in the gastrointestinal tract. However, possible non‐specific effects of the inhibitors should be considered.