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链脲佐菌素诱导的糖尿病大鼠血浆组胺浓度的变化

Changes in plasma histamine concentration in the streptozotocin-diabetic rat.

作者信息

Hollis T M, Kern J A, Enea N A, Cosgarea A J

出版信息

Exp Mol Pathol. 1985 Aug;43(1):90-6. doi: 10.1016/0014-4800(85)90058-9.

Abstract

Plasma histamine concentrations were measured in rats made diabetic via jugular vein injection of streptozotocin and held 4 weeks following diabetes diagnosis. At least 15 diabetic animals received insulin (6-8 U/day) or alpha-hydrazinohistidine (alpha-HH) for the last week of the holding period. alpha-HH is a specific inhibitor of histidine decarboxylase (HD), the principle histamine-forming enzyme in mammals. Plasma histamine concentrations, expressed as means and mean standard errors (ng/ml) were as follows: control, 25.5 +/- 2.4; diabetic, 47.1 +/- 5.2; diabetic-insulin, 34.6 +/- 2.9; diabetic-alpha-HH, 28.1 +/- 2.1. These data indicate that in experimental diabetes there is an expansion of the nascent, or inducible histamine pool, an increase which is reflected by increased circulating plasma histamine. This may be one component mediating altered microvessel as well as large vessel permeability characteristics, an underlying component of both diabetic microangiopathy and macroangiopathy.

摘要

通过颈静脉注射链脲佐菌素使大鼠患糖尿病,并在糖尿病诊断后维持4周,然后测量其血浆组胺浓度。在维持期的最后一周,至少15只糖尿病动物接受胰岛素(6 - 8单位/天)或α-肼基组氨酸(α-HH)治疗。α-HH是组氨酸脱羧酶(HD)的特异性抑制剂,HD是哺乳动物中主要的组胺形成酶。血浆组胺浓度以平均值和平均标准误(ng/ml)表示如下:对照组,25.5±2.4;糖尿病组,47.1±5.2;糖尿病-胰岛素组,34.6±2.9;糖尿病-α-HH组,28.1±2.1。这些数据表明,在实验性糖尿病中,新生的或可诱导的组胺池有所扩大,循环血浆组胺增加反映了这一增长。这可能是介导微血管以及大血管通透性改变的一个因素,而微血管病变和大血管病变均以此为潜在因素。

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