Effect of cholinergic blockade on inhibited GH secretion by feeding and intraruminal SCFA infusion in sheep
Laboratory of Animal Production, Department of Animal Science, Obihiro University of Agriculture and Veterinary Medicine, Inada-cho, Obihiro 080, Japan The effect of cholinergic blockade on suppressed growth hormone (GH) secretion caused by feeding or the intraruminal infusion of an acetate, propion...
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Veröffentlicht in: | American journal of physiology: endocrinology and metabolism 1998-01, Vol.274 (1), p.E45-E51 |
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Zusammenfassung: | Laboratory of Animal Production, Department of Animal Science,
Obihiro University of Agriculture and Veterinary Medicine, Inada-cho,
Obihiro 080, Japan
The effect of cholinergic blockade on suppressed growth hormone
(GH) secretion caused by feeding or the intraruminal infusion of an
acetate, propionate, and butyrate mixture (107 and 214 µmol · kg 1 · min 1
over 6 h) was examined in ovariectomized ewes. Intraruminal infusion at
the rate of 107 µmol · kg 1 · min 1
increased peripheral plasma short-chain fatty acid (SCFA)
concentrations to approximately the physiological levels noted after
feeding. Plasma GH was markedly suppressed by feeding and at both the
107 and 214 µmol · kg 1 · min 1
SCFA infusion rates; however, cholinergic blocking agents completely blocked the suppressed GH secretion after feeding and only at the 107 µmol · kg 1 · min 1
infusion rate. Plasma glucose increased at both infusion rates, and the
plasma free fatty acids decreased after feeding and at both infusion
rates. However, both metabolites were unchanged relative to the saline
control after the injection of the cholinergic antagonists. It is
suggested that the decrease in plasma GH observed after feeding and a
near-physiological ruminal SCFA increment is mediated via the
parasympathetic nerve and not by pharmacological ruminal SCFA
increments attributed to other pathways.
growth hormone; short-chain fatty acids; parasympathetic
nerve |
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ISSN: | 0002-9513 0193-1849 2163-5773 1522-1555 |
DOI: | 10.1152/ajpendo.1998.274.1.e45 |