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链脲佐菌素诱导糖尿病小鼠大脑中组胺代谢的变化。

Changes in histamine metabolism in the brains of mice with streptozotocin-induced diabetes.

作者信息

Nishibori M, Oishi R, Itoh Y, Saeki K

机构信息

Department of Pharmacology, Okayama University Medical School, Japan.

出版信息

J Neurochem. 1989 May;52(5):1375-81. doi: 10.1111/j.1471-4159.1989.tb09182.x.

Abstract

Histamine (HA) metabolism in the brain of mice with streptozotocin (STZ)-induced diabetes was examined. The levels of tele-methylhistamine (t-MH), a major metabolite of brain HA, significantly increased 3 and 4 weeks after STZ injection. However, the HA turnover rates in the diabetic mice, determined from the accumulation of t-MH after the administration of pargyline, were not different from the control values when the animals were allowed free access to food. When the mice were starved for 15 h 4 weeks after STZ treatment, the brain levels of L-histidine decreased significantly, whereas HA turnover increased significantly. Such changes were not observed in starved control mice. Histidine decarboxylase or HA N-methyltransferase activity did not change after starvation in either diabetic or control mice. These results show that the histaminergic (HAergic) activity in the brains of diabetic mice remains within normal range as long as the animals are allowed free access to food. However, they also indicate that a marked enhancement of HAergic activity accompanied by a decrease in the brain L-histidine level occurs in starved diabetic mice.

摘要

研究了链脲佐菌素(STZ)诱导的糖尿病小鼠脑内组胺(HA)的代谢情况。脑HA的主要代谢产物——3-甲基组胺(t-MH)的水平在STZ注射后3周和4周显著升高。然而,当动物可以自由进食时,根据帕吉林给药后t-MH的积累情况测定的糖尿病小鼠的HA周转率与对照值并无差异。在STZ处理4周后,当小鼠饥饿15小时,脑内L-组氨酸水平显著降低,而HA周转率显著增加。饥饿的对照小鼠未观察到此类变化。饥饿后,糖尿病小鼠和对照小鼠的组氨酸脱羧酶或HA N-甲基转移酶活性均未改变。这些结果表明,只要动物可以自由进食,糖尿病小鼠脑内的组胺能(HAergic)活性就保持在正常范围内。然而,它们也表明,饥饿的糖尿病小鼠会出现HAergic活性显著增强,同时脑内L-组氨酸水平降低的情况。

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