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胍那苄和胍法辛对大鼠下颌下腺和腮腺突触后α2-肾上腺素能受体的影响。

Effects of guanabenz and guanfacine on postsynaptic alpha 2-adrenoceptors in the rat submaxillary and parotid glands.

作者信息

Kaniucki M D, Elverdin J C, Stefano F J, Perec C J

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1985 May;329(3):289-92. doi: 10.1007/BF00501882.

Abstract

The effects of two alpha 2-agonists (guanfacine and guanabenz) on both the submaxillary and parotid gland of the rat were studied. Whereas guanfacine in doses ranging between 1,000 and 30,000 micrograms/kg i.v. produced an immediate and persistent secretion of saliva from the submaxillary gland, guanabenz in doses as high as 40,000 micrograms/kg did not induce measurable secretion either from the parotid or the submaxillary gland. Secretion elicited by guanfacine was not modified by yohimbine (300 micrograms/kg) but was abolished by prazosin (100 micrograms/kg). In both glands, low doses of either guanabenz (10 micrograms/kg) or guanfacine (100 micrograms/kg) markedly inhibited the secretory responses induced by noradrenaline, methacholine and substance P, but not that induced by isoprenaline. The inhibition caused by the alpha 2-agonists was greater for noradrenaline than for either methacholine or substance P. Blockade of alpha 2-adrenoceptors with yohimbine (300 micrograms/kg) did not modify the response to noradrenaline, methacholine or substance P in either gland. However, the same dose of yohimbine injected 5 min before the alpha 2-agonists prevented the inhibitory effects of guanfacine and guanabenz on the response induced by either one of the three sialagogic agents. Guanabenz (10 micrograms/kg) did not modify the increase in mean blood pressure observed after the different doses of noradrenaline employed to induce salivary secretion. Guanabenz (10 micrograms/kg) and guanfacine (100 micrograms/kg) did not change the time course of the secretion elicited by either noradrenaline, methacholine or substance P, since the degree of inhibition was of similar magnitude at all the periods of time analyzed.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了两种α2-激动剂(胍法辛和胍那苄)对大鼠颌下腺和腮腺的影响。静脉注射剂量在1000至30000微克/千克之间的胍法辛可使颌下腺立即持续分泌唾液,而高达40000微克/千克剂量的胍那苄对腮腺和颌下腺均未诱导出可测量的分泌。胍法辛引起的分泌不受育亨宾(300微克/千克)影响,但被哌唑嗪(100微克/千克)消除。在这两种腺体中,低剂量的胍那苄(10微克/千克)或胍法辛(100微克/千克)均显著抑制去甲肾上腺素、乙酰甲胆碱和P物质诱导的分泌反应,但不抑制异丙肾上腺素诱导的分泌反应。α2-激动剂对去甲肾上腺素的抑制作用比对乙酰甲胆碱或P物质的抑制作用更强。用育亨宾(300微克/千克)阻断α2-肾上腺素能受体对两种腺体中去甲肾上腺素、乙酰甲胆碱或P物质的反应均无影响。然而,在α2-激动剂注射前5分钟注射相同剂量的育亨宾可防止胍法辛和胍那苄对三种催涎剂之一诱导的反应的抑制作用。胍那苄(10微克/千克)不改变用于诱导唾液分泌的不同剂量去甲肾上腺素后观察到的平均血压升高。胍那苄(10微克/千克)和胍法辛(100微克/千克)不改变去甲肾上腺素、乙酰甲胆碱或P物质引起的分泌的时间进程,因为在所有分析时间段内抑制程度相似。(摘要截短至250字)

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