Effect of short-chain fatty acids on cyclic 3′,5′-guanosine monophosphate-mediated colonic secretion
Short chain fatty acids (SCFA) prevent and reverse cyclic 3′,5′-adenosine monophosphate (cAMP) but not Ca 2+-mediated Cl − secretion. Mucosal [HCO 3 −] i has an opposite effect on these secretagogues. We examined whether SCFA and [HCO 3 −] i affect cyclic 3′,5′-guanosine monophosphate (cGMP)-induced...
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Veröffentlicht in: | Comparative biochemistry and physiology. Part A, Molecular & integrative physiology Molecular & integrative physiology, 1999-10, Vol.124 (2), p.169-178 |
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Zusammenfassung: | Short chain fatty acids (SCFA) prevent and reverse cyclic 3′,5′-adenosine monophosphate (cAMP) but not Ca
2+-mediated Cl
− secretion. Mucosal [HCO
3
−]
i has an opposite effect on these secretagogues. We examined whether SCFA and [HCO
3
−]
i affect cyclic 3′,5′-guanosine monophosphate (cGMP)-induced secretion. Stripped segments of male Sprague–Dawley rat (
Rattus norvegicus) proximal and distal colon, and cultured T84 cells were studied in Ussing chambers, and pH
i and [HCO
3
−]
i were determined. Mucosal [cGMP] was measured in proximal colon. In T84 cells, the increase in Cl
− secretion (measured as
I
sc) induced by mucosal 0.25 μM
Escherichia coli heat-stable enterotoxin (ST
a) was prevented/reversed by bilateral 50 mM Na
+ butyrate (71%/73%), acetate (58%/76%), propionate (68%/73%) and (poorly metabolized) isobutyrate (80%/79%). In proximal colon in HCO
3
− Ringer, basal Cl
− secretion was not affected by [HCO
3
−]
i or 25 mM butyrate. Mucosal 0.25 μM ST
a decreased net Na
+ and Cl
− absorption. Bilateral but not mucosal 25 mM SCFA reversed ST
a-induced effects on Na
+ absorption and Cl
− secretion. Bilateral and mucosal 25 mM SCFA but not [HCO
3
−]
i prevented ST
a-induced Cl
− secretion and increases in mucosal [cGMP]. ST
a did not produce Cl
− secretion in distal colon. It was concluded that SCFA but not [HCO
3
−]
i can prevent and reverse cGMP-induced colonic Cl
− secretion. |
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ISSN: | 1095-6433 1531-4332 |
DOI: | 10.1016/S1095-6433(99)00107-5 |