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Inhibition of acid-induced hyperaemia in the rat stomach by endogenous NK2 receptor ligands.

机译:内源性NK2受体配体抑制酸诱导的大鼠胃充血。

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摘要

Since exogenously applied tachykinins (substance P and neurokinin A) prevent the neurogenic hyperaemia which is elicited by acid back-diffusion in the rat stomach, we investigated whether endogenous tachykinins would act in a similar manner. Acid back-diffusion, induced by perfusing the stomach with 15% ethanol in the presence of 0.05 M HCI, increased gastric mucosal blood flow (GMBF) by 60-100% as determined by hydrogen clearance in urethane-anaesthetized rats. This response remained unchanged after pretreatment with the tachykinin NK1 receptor antagonist SR 140,333 (300 nmol/kg) but tended to be enhanced by the NK2 receptor antagonist MEN 10,627 (200 nmol/kg). When given during ongoing acid back-diffusion, MEN 10,627 significantly enhanced the acid-evoked vasodilatation as compared with vehicle or SR 140,333. We conclude that endogenously released tachykinins, acting via NK2 receptors, limit the gastric hyperaemic response to acid.
机译:由于外源性速激肽(物质P和神经激肽A)可预防大鼠胃酸反扩散引起的神经源性充血,因此我们研究了内源性速激肽是否会以类似方式起作用。如在尿烷麻醉的大鼠中通过氢清除确定,在0.05 M HCl存在下用15%乙醇灌注胃引起的酸反扩散,使胃粘膜血流量(GMBF)增加了60-100%。用速激肽NK1受体拮抗剂SR 140,333(300 nmol / kg)预处理后,该反应保持不变,但NK2受体拮抗剂MEN 10,627(200 nmol / kg)往往会增强这种反应。与持续溶媒或SR 140,333相比,MEN 10,627在持续的酸反扩散过程中给予时,可显着增强酸诱发的血管舒张。我们得出的结论是,内源性释放的速激肽通过NK2受体起作用,限制了胃对酸的充血反应。

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