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兔膝关节血管的神经介导反应。

Nerve-mediated responses of blood vessels in the rabbit knee joint.

作者信息

Khoshbaten A, Ferrell W R

机构信息

Institute of Physiology, University of Glasgow, UK.

出版信息

J Vasc Res. 1993 Mar-Apr;30(2):102-7. doi: 10.1159/000158981.

Abstract

Blood vessels in the anterior region of the knee joint of anaesthetised rabbits showed a biphasic response to the electrical stimulation (10 Hz, 1 ms width, 10 V amplitude) of nerve fibres supplying the knee, as measured by laser Doppler flowmetry. The response consisted of vasoconstriction during nerve stimulation followed by a prolonged dilatation. The vasoconstrictor response was mediated by noradrenaline acting mainly via alpha 1-adrenoceptors as it was substantially reduced by close intra-arterial injection of the alpha-adrenergic antagonist phentolamine (approximately 50% reduction) and the selective alpha 1-adrenergic antagonist prazosin (approximately 50% reduction) but not by the alpha 2-antagonist rauwolscine. Further studies involving prolonged (2-hour) close intra-arterial infusion of prazosin gave a approximately 50% reduction of the constrictor response with a concentration of 10(-5) M and approximately 95% reduction when the concentration was raised to 10(-4) M. At the higher prazosin concentration responses to close intra-arterial injection of the alpha 1-agonist phenylephrine were substantially reduced but responses to the alpha 2-agonists clonidine and UK-14304 were not significantly influenced. Infusions of the alpha 2 antagonist CH 38083 failed to inhibit nerve-mediated vasoconstriction at 10(-5) or 10(-4) M. There did not appear to be a purinergic component, as the constrictor response was unaffected by the P2X desensitiser alpha,beta-methylene adenosine 5'-triphosphate. The dilator response appeared to be mediated principally by substance P (presumably released from sensory C fibers) as it was substantially reduced by intraarticular injection of substance P antagonist D-Pro4D-Trp7,9,10-SP(4-11).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过激光多普勒血流仪测量发现,麻醉兔膝关节前部的血管对供应膝关节的神经纤维进行电刺激(10赫兹,1毫秒宽度,10伏幅度)时呈现双相反应。该反应包括神经刺激期间的血管收缩,随后是长时间的扩张。血管收缩反应主要由去甲肾上腺素通过α1 - 肾上腺素能受体介导,因为通过动脉内近距离注射α - 肾上腺素能拮抗剂酚妥拉明(约减少50%)和选择性α1 - 肾上腺素能拮抗剂哌唑嗪(约减少50%)可使其显著降低,但α2 - 拮抗剂育亨宾则无此作用。进一步研究发现,长时间(2小时)动脉内近距离输注哌唑嗪,浓度为10^(-5) M时收缩反应约降低50%,浓度升至10^(-4) M时约降低95%。在较高哌唑嗪浓度下,动脉内近距离注射α1 - 激动剂去氧肾上腺素的反应显著降低,但对α2 - 激动剂可乐定和UK - 14304的反应无明显影响。输注α2拮抗剂CH 38083在10^(-5)或10^(-4) M时未能抑制神经介导的血管收缩。似乎不存在嘌呤能成分,因为收缩反应不受P2X脱敏剂α,β - 亚甲基腺苷5'-三磷酸的影响。扩张反应似乎主要由P物质介导(可能从感觉C纤维释放),因为关节内注射P物质拮抗剂D - Pro4D - Trp7,9,10 - SP(4 - 11)可使其显著降低。(摘要截选至250字)

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