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经前情期用p,p'-滴滴涕处理后的5-羟色胺能变化

Serotonergic changes following proestrous treatment with p,p'-DDT.

作者信息

Uphouse L, Eckols K, Croissant D, Stewart G

机构信息

Department of Biology, Texas Woman's University, Denton 76204.

出版信息

Neurotoxicology. 1990 Fall;11(3):533-8.

PMID:1704493
Abstract

The effects of 25 and 75 mg/kg p,p'-DDT on the CNS serotonergic system were examined in proestrous female rats. Females were treated with p,p'-DDT on the morning of proestrus and were sacrificed that evening. Levels of serotonin (5-HT) and its major metabolite, 5-hydroxyindoleacetic acid (5-HIAA), were examined in cortex, hippocampus, hypothalamus and preoptic areas. The binding of 3'-8-OH-DPAT [2-hydroxy-2-N, N-(di-propylamino)-tetralin], an agonist for 5-HT1A receptors, was examined in hippocampus and frontal cortex. P,p'-DDT decreased the level of 5-HT in frontal cortex and hippocampus. Elevations in 5-HIAA were present in the hypothalamus but only at the higher dose of p,p'-DDT. The dose of 25 mg/kg p,p'-DDT produced an increase in the Bmax for 3H-8-OH-DPAT binding to frontal cortical and hippocampal membranes. Membrane preparations from females given 75 mg/kg p,p'-DDT fell into two categories. Some were similar to the control but with a slightly higher Kd; others could not be analyzed by traditional linear or nonlinear regression procedures because they showed a constant proportion of bound label, independent of the concentration of 3H-ligand in the reaction. In vitro, p,p'-DDT did not compete with 3H-8-OH-DPAT for binding to cortical membranes so it is unlikely that residual pesticide in the membrane preparation accounted for the binding results. These binding results are particularly interesting because, in previous studies, the dose of 25 mg/kg p,p'-DDT was shown to be more potent than 75 mg/kg p,p'-DDT in reducing female rodent lordosis behavior.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在动情前期的雌性大鼠中研究了25毫克/千克和75毫克/千克的p,p'-滴滴涕(p,p'-DDT)对中枢神经系统5-羟色胺能系统的影响。雌性大鼠在动情前期的早晨接受p,p'-DDT处理,并于当晚处死。检测了皮质、海马体、下丘脑和视前区中5-羟色胺(5-HT)及其主要代谢产物5-羟基吲哚乙酸(5-HIAA)的水平。检测了海马体和额叶皮质中5-HT1A受体激动剂3'-8-羟基二丙基氨基四氢萘(3'-8-OH-DPAT)的结合情况。p,p'-DDT降低了额叶皮质和海马体中5-HT的水平。下丘脑5-HIAA水平升高,但仅在较高剂量的p,p'-DDT时出现。25毫克/千克的p,p'-DDT剂量使3H-8-OH-DPAT与额叶皮质和海马体膜结合的Bmax增加。给予75毫克/千克p,p'-DDT的雌性大鼠的膜制剂分为两类。一些与对照组相似,但解离常数(Kd)略高;另一些则无法通过传统的线性或非线性回归程序进行分析,因为它们显示出固定比例的结合标记,与反应中3H配体的浓度无关。在体外,p,p'-DDT不与3H-8-OH-DPAT竞争结合皮质膜,因此膜制剂中的残留农药不太可能是结合结果的原因。这些结合结果特别有趣,因为在先前的研究中,25毫克/千克的p,p'-DDT剂量在降低雌性啮齿动物脊柱前凸行为方面比75毫克/千克的p,p'-DDT更有效。(摘要截断于250字)

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