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药物对脑及外周组织去甲肾上腺素含量的影响及其意义。

Effect of drugs on the noradrenaline content of brain and peripheral tissues and its significance.

作者信息

SANAN S, VOGT M

出版信息

Br J Pharmacol Chemother. 1962 Feb;18(1):109-27. doi: 10.1111/j.1476-5381.1962.tb01155.x.

Abstract

Large single doses of methoserpidine (12 mg/kg) given to rabbits lowered the noradrenaline content of sympathetic ganglia but not that of brain; no sedation was observed. Cats responded to doses ranging from 12 to 0.5 mg/kg with loss of noradrenaline from ganglia as well as from brain, and were sedated by the drug. The effect in man resembles that in the rabbit. Only within the group of reserpine-like drugs do sedation and loss in hypothalamic noradrenaline run parallel. These effects are therefore not causally related. Guanethidine lowers the noradrenaline content of sympathetic ganglia (cats and rabbits), but this effect does not explain the blocking action of the drug on the adrenergic nerve. Effects on the noradrenaline of the brain are variable and may be caused reflexly rather than by direct central action of guanethidine. Repeated intravenous injections of dimethylphenylpiperazinium iodide for a period of 4 hr did not produce any significant change in the noradrenaline content of ganglia or brain of rabbits. In contrast, dexamphetamine (20 mg/kg) produced a small but significant mean fall in noradrenaline content of the superior cervical ganglia and in that of the brain, but the effects were not seen in every rabbit. Prolonged administration of the mono-amine oxidase inhibitors pheniprazine and phenylhydrazinobutane raised the noradrenaline content of the brain of rabbits but not that of cats, whereas it raised the noradrenaline of the ganglia of cats but not (or rarely) that of rabbits. The question of correlation between a rise in the noradrenaline content of the brain and certain clinical signs is discussed. Finally, a comparison is made in rabbits between the changes produced by drugs in the noradrenaline content of the heart and of the superior cervical ganglion. The changes run parallel and are only occasionally more pronounced in the heart.

摘要

给兔子大剂量单次注射美索舍平(12毫克/千克)可降低交感神经节中的去甲肾上腺素含量,但不会降低脑内的去甲肾上腺素含量;未观察到镇静作用。猫对12至0.5毫克/千克的剂量有反应,神经节和脑内的去甲肾上腺素均减少,且该药物使猫产生镇静作用。该药物对人的作用类似于对兔子的作用。只有在利血平样药物组中,镇静作用和下丘脑去甲肾上腺素减少才是平行的。因此,这些作用并非因果相关。胍乙啶可降低交感神经节(猫和兔子)中的去甲肾上腺素含量,但这种作用并不能解释该药物对肾上腺素能神经的阻断作用。胍乙啶对脑内去甲肾上腺素的作用多变,可能是反射性引起的,而非通过其对中枢的直接作用。对兔子连续4小时静脉注射碘化二甲基苯哌嗪,神经节或脑内的去甲肾上腺素含量未发生任何显著变化。相比之下,右旋苯丙胺(20毫克/千克)可使颈上神经节和脑内的去甲肾上腺素含量出现小幅度但显著的平均下降,但并非每只兔子都出现这种效应。长期给予单胺氧化酶抑制剂苯乙肼和苯肼丁烷可提高兔子脑内的去甲肾上腺素含量,但对猫则无此作用,而它可提高猫神经节中的去甲肾上腺素含量,但对兔子则无此作用(或很少有此作用)。文中讨论了脑内去甲肾上腺素含量升高与某些临床体征之间的相关性问题。最后,对兔子进行了比较,观察药物对心脏和颈上神经节中去甲肾上腺素含量产生的变化。这些变化是平行的,只是偶尔在心脏中的变化更为明显。

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