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交感神经去神经支配不会改变大鼠输精管中α-1肾上腺素能受体的密度或特性。

Sympathetic denervation does not alter the density or properties of alpha-1 adrenergic receptors in rat vas deferens.

作者信息

Abel P W, Johnson R D, Martin T J, Minneman K P

出版信息

J Pharmacol Exp Ther. 1985 Jun;233(3):570-7.

PMID:2989488
Abstract

Alpha-1 adrenergic receptors in surgically denervated rat vas deferens were studied using radioligand binding assays of [125I] BE 2254 ([125I]BE) and contraction measurements. Scatchard analysis of saturation isotherms of specific [125I]BE binding showed no change in the affinity or density of binding sites 4, 7 or 14 days after denervation of rat vas deferens. The potency of norepinephrine in inhibiting specific [125I]BE binding was also unchanged 7 days after denervation of vas deferens. The potency of phenylephrine in causing contraction in vitro did not change 4, 7 or 14 days after denervation of vas deferens; however, there was a significant increase in the maximum contractile response to phenylephrine at all time points. After partial inactivation of alpha-1 adrenergic receptors in vitro with phenoxybenzamine, there was an equivalent reduction in the number of [125I]BE binding sites in the control and 14-day denervated vas deferens. The equilibrium dissociation constants calculated from contractile measurements for norepinephrine were the same in the control and denervated tissues. However, there was a 2.2-fold increase in contractile sensitivity to norepinephrine 14 days after denervation and a 3.6-fold increase in contractile sensitivity to methacholine 7 days after denervation. These results show that surgical denervation of the rat vas deferens results in an increase in contractile sensitivity to norepinephrine and methacholine and an increase in maximum contraction. However, there is no change in alpha-1 adrenergic receptor density or properties at any time after denervation. Thus, alterations in alpha-1 adrenergic receptors do not contribute to contractile supersensitivity of denervated rat vas deferens.

摘要

利用[125I]BE 2254([125I]BE)的放射性配体结合试验和收缩测量,对手术去神经大鼠输精管中的α-1肾上腺素能受体进行了研究。对特异性[125I]BE结合的饱和等温线进行Scatchard分析表明,大鼠输精管去神经后4、7或14天,结合位点的亲和力或密度没有变化。输精管去神经7天后,去甲肾上腺素抑制特异性[125I]BE结合的效力也未改变。苯肾上腺素在体外引起收缩的效力在输精管去神经后4、7或14天没有变化;然而,在所有时间点,对苯肾上腺素的最大收缩反应均显著增加。在用酚苄明体外部分灭活α-1肾上腺素能受体后,对照和去神经14天的输精管中[125I]BE结合位点的数量有同等程度的减少。根据收缩测量计算得出的去甲肾上腺素的平衡解离常数在对照组织和去神经组织中是相同的。然而,去神经14天后对去甲肾上腺素的收缩敏感性增加了2.2倍,去神经7天后对乙酰甲胆碱的收缩敏感性增加了3.6倍。这些结果表明,大鼠输精管手术去神经导致对去甲肾上腺素和乙酰甲胆碱的收缩敏感性增加以及最大收缩增加。然而,去神经后任何时候α-1肾上腺素能受体的密度或特性均无变化。因此,α-1肾上腺素能受体的改变并不导致去神经大鼠输精管的收缩超敏反应。

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