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Am J Physiol Regul Integr Comp Physiol ; 302(10): R1176-83, 2012 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-22422667

RESUMO

Pythons exhibit a doubling of heart rate when metabolism increases several times during digestion. Pythons, therefore, represent a promising model organism to study autonomic cardiovascular regulation during the postprandial state, and previous studies show that the postprandial tachycardia is governed by a release of vagal tone as well as a pronounced stimulation from nonadrenergic, noncholinergic (NANC) factors. Here we show that infusion of plasma from digesting donor pythons elicit a marked tachycardia in fasting snakes, demonstrating that the NANC factor resides in the blood. Injections of the gastrin and cholecystokinin receptor antagonist proglumide had no effect on double-blocked heart rate or blood pressure. Histamine has been recognized as a NANC factor in the early postprandial period in pythons, but the mechanism of its release has not been identified. Mast cells represent the largest repository of histamine in vertebrates, and it has been speculated that mast cells release histamine during digestion. Treatment with the mast cell stabilizer cromolyn significantly reduced postprandial heart rate in pythons compared with an untreated group but did not affect double-blocked heart rate. While this study indicates that histamine induces postprandial tachycardia in pythons, its release during digestion is not stimulated by gastrin or cholecystokinin nor is its release from mast cells a stimulant of postprandial tachycardia.


Assuntos
Boidae/fisiologia , Digestão/fisiologia , Frequência Cardíaca/fisiologia , Histamina/metabolismo , Período Pós-Prandial/fisiologia , Animais , Pressão Sanguínea/efeitos dos fármacos , Pressão Sanguínea/fisiologia , Cromolina Sódica/farmacologia , Gastrinas/antagonistas & inibidores , Gastrinas/efeitos dos fármacos , Antagonistas dos Receptores Histamínicos/farmacologia , Mastócitos/efeitos dos fármacos , Mastócitos/metabolismo , Modelos Animais , Proglumida/farmacologia , Receptores da Colecistocinina/antagonistas & inibidores , Receptores da Colecistocinina/efeitos dos fármacos , Taquicardia/fisiopatologia
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