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大鼠中缝背核电刺激诱导促黄体生成素释放变化所介导的神经递质受体分析

Analysis of neurotransmitter receptors mediating changes in LH release induced by electrical stimulation of the dorsal raphe nucleus in the rat.

作者信息

Johnson J H, Kitts C S

机构信息

Department of Anatomy, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298.

出版信息

J Neurosci Res. 1991 Aug;29(4):520-6. doi: 10.1002/jnr.490290412.

Abstract

We report studies of neurotransmitter and receptor species mediating the inhibition of LH release in ovariectomized (OVX) rats and stimulation in OVX estrogen-primed rats induced by electrical stimulation of the dorsal raphe nucleus (DRN). Attempts were made to block effects of stimulation of the DRN in groups of four to nine ovariectomized rats with or without priming with estradiol benzoate (EB) by pretreatment with the 5HT receptor antagonists ketanserin, methysergide, or metergoline; the alpha-adrenergic antagonist phenoxybenzamine; or the opiate antagonist naltrexone. Blood samples were collected via jugular cannulae from the unanesthetized rats at 10-min intervals before and during electrical stimulation of the DRN, and assayed by double antibody radioimmunoassay for LH. To test the effect of stimulation, data from animals in each treatment group were subjected to analysis of variance to obtain the contrast matrix including prestimulation and stimulation time points of interest. The contrast matrix was then used to construct an F ratio and thereby to evaluate the level of significance. In unprimed OVX rats the sustained decrease in plasma LH concentration during stimulation was prevented in rats pretreated with ketanserin or phenoxybenzamine. Methysergide pretreatment delayed the inhibitory effect of DRN electrical stimulation for 30 min, whereas metergoline and naltrexone were ineffective. In EB-primed animals the increase in plasma LH observed during stimulation was prevented in rats pretreated with metergoline, and reversed in those receiving naltrexone. Ketanserin limited the duration of the increase to 10 min, while phenoxybenzamine and methysergide had no significant effect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们报告了关于神经递质和受体种类的研究,这些神经递质和受体介导了去卵巢(OVX)大鼠促黄体生成素(LH)释放的抑制,以及在去卵巢并用雌激素预处理的大鼠中,由电刺激中缝背核(DRN)所诱导的LH释放的刺激。我们尝试通过用5-羟色胺(5HT)受体拮抗剂酮色林、麦角新碱或美替拉林;α-肾上腺素能拮抗剂酚苄明;或阿片拮抗剂纳曲酮进行预处理,来阻断电刺激DRN对四至九只去卵巢大鼠组(无论是否用苯甲酸雌二醇(EB)预处理)的影响。在电刺激DRN之前和期间,每隔10分钟通过颈静脉插管从未麻醉的大鼠采集血样,并通过双抗体放射免疫分析法测定LH。为了测试刺激的效果,对每个治疗组动物的数据进行方差分析,以获得包括感兴趣的刺激前和刺激时间点的对比矩阵。然后使用对比矩阵构建F比率,从而评估显著性水平。在未预处理的OVX大鼠中,用酮色林或酚苄明预处理的大鼠在刺激期间血浆LH浓度的持续下降得到了预防。麦角新碱预处理使DRN电刺激的抑制作用延迟了30分钟,而美替拉林和纳曲酮则无效。在用EB预处理的动物中,用美替拉林预处理的大鼠在刺激期间观察到的血浆LH升高得到了预防,而在接受纳曲酮的大鼠中则逆转。酮色林将升高的持续时间限制在10分钟,而酚苄明和麦角新碱没有显著影响。(摘要截断于250字)

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