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年轻自发性高血压大鼠的肠系膜血管反应

Mesenteric vascular responses of young spontaneously hypertensive rats.

作者信息

Kong J Q, Taylor D A, Fleming W W

机构信息

Department of Pharmacology and Toxicology, West Virginia University Health Sciences Center, Morgantown.

出版信息

J Pharmacol Exp Ther. 1991 Jul 1;258(1):13-7.

PMID:2072289
Abstract

Frequency-responses curves for nerve stimulation and dose-response curve for norepinephrine, 5-hydroxytryptamine potassium chloride, vasopressin and acetylcholine (ACh) were determined in isolated, perfused mesenteric vascular beds from young (approximately 5 weeks) spontanelouly hypertensive (SHR) and Wistar Kyoto rats. Although mean systolic blood pressure (measured by tail cuff plethysmography) was slightly higher in the SHR, this difference was not significant. Slopes and maximum responses were increased significantly for nerve stimulation and all agonists. The basal perfusion pressure was also significantly elevated in the SHR. These differences are consistent with existing evidence that structural changes occur in blood vessels of SHR at an early stage and probably precede development of hypertension. Such structural changes could therefore contribute to development of the hypertension. Cocaine (1 microM) markedly increased responses to nerve stimulation and bolus injections of norepinephrine in preparations from SHR with little or no effect on such responses in Wistar Kyoto preparations, a result consistent with the known greater density of noradrenergic nerves in SHR vasculature. In the presence of cocaine, there was unmasked a selective super-sensitivity (significantly lower ED50) to norepinephrine in the SHR. Thus SHR mesenteric vessels may possess an alteration in adrenoreceptors or their coupling to other cellular mechanisms. Responses to ACh revealed no indication of a deficient endothelial mediated relaxation. An altered media:lumen ratio of small arteries, hypernoradrenergic innervation and supersensitivity to the transmitter may contribute to development of hypertension.

摘要

在来自年轻(约5周龄)自发性高血压(SHR)大鼠和Wistar Kyoto大鼠的离体灌注肠系膜血管床中,测定了神经刺激的频率响应曲线以及去甲肾上腺素、5-羟色胺、氯化钾、血管加压素和乙酰胆碱(ACh)的剂量响应曲线。尽管SHR的平均收缩压(通过尾袖体积描记法测量)略高,但这种差异并不显著。神经刺激和所有激动剂的斜率和最大反应均显著增加。SHR的基础灌注压也显著升高。这些差异与现有证据一致,即SHR血管在早期就发生了结构变化,可能早于高血压的发展。因此,这种结构变化可能有助于高血压的发展。可卡因(1 microM)显著增加了SHR制备物中对神经刺激和去甲肾上腺素推注的反应,而对Wistar Kyoto制备物中的此类反应几乎没有影响,这一结果与已知的SHR血管中去甲肾上腺素能神经密度更高一致。在可卡因存在的情况下,SHR中对去甲肾上腺素出现了选择性超敏反应(ED50显著降低)。因此,SHR肠系膜血管可能在肾上腺素能受体或其与其他细胞机制的偶联方面存在改变。对ACh的反应未显示内皮介导的舒张功能缺陷。小动脉中中膜与管腔比例的改变、去甲肾上腺素能神经支配过度以及对递质的超敏反应可能有助于高血压的发展。

相似文献

1
Mesenteric vascular responses of young spontaneously hypertensive rats.年轻自发性高血压大鼠的肠系膜血管反应
J Pharmacol Exp Ther. 1991 Jul 1;258(1):13-7.
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Evidence for enhanced inhibitory modulation by cyclooxygenase products of noradrenergic neurotransmission in the mesenteric vasculature of young spontaneously hypertensive rats.年轻自发性高血压大鼠肠系膜血管中去甲肾上腺素能神经传递的环氧化酶产物增强抑制性调节的证据。
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Release of endogenous NE from the mesenteric vasculature of WKY and SHR in response to PNS.在副交感神经系统(PNS)作用下,从WKY和SHR的肠系膜血管中释放内源性去甲肾上腺素(NE)。
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Angiotensin-converting enzyme inhibition attenuates arterial constrictor responses in experimental hypertension.血管紧张素转换酶抑制可减弱实验性高血压中的动脉收缩反应。
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Defective modulation of noradrenergic neurotransmission by exogenous prostaglandins in aging spontaneously hypertensive rats.衰老自发性高血压大鼠中外源性前列腺素对去甲肾上腺素能神经传递的调节缺陷。
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Potentiation of pressor responses to serotonin by ketamine in isolated perfused rat mesentery.氯胺酮对离体灌注大鼠肠系膜中血清素升压反应的增强作用。
J Cardiovasc Pharmacol. 1986 Jul-Aug;8(4):765-70.

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