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自发性高血压对鞘内烟碱激动剂的增强反应。

Augmented responses to intrathecal nicotinic agonists in spontaneous hypertension.

作者信息

Khan I M, Printz M P, Yaksh T L, Taylor P

机构信息

Department of Pharmacology, University of California, San Diego, La Jolla, CA 92093.

出版信息

Hypertension. 1994 Nov;24(5):611-9. doi: 10.1161/01.hyp.24.5.611.

Abstract

Abnormal central cholinergic activity has been reported to be responsible in part for the pathogenesis of high blood pressure in spontaneously hypertensive rats (SHR). Administration of cholinergic agonists in brain and spinal cord results in exaggerated pressor responses in SHR. Studies to date have focused largely on the muscarinic cholinergic system. Recently, we demonstrated that intrathecal administration of nicotinic agonists results in pressor, tachycardic, and irritation responses. In the present study we examine the cardiovascular and behavioral responses to nicotine and cytisine administered intrathecally in La Jolla strain (LJ) SHRLJ and age-matched Wistar-Kyoto (WKYLJ) rats. Nicotinic agonists produced augmented pressor, heart rate, and irritation responses in SHRLJ compared with normotensive rats. In both SHRLJ and WKYLJ rats, cytisine elicited a greater nociceptive response and greater spinobulbar component to the pressor response than nicotine. SHRLJ and WKYLJ rats also differ in that the SHRLJ strain shows a diminished tendency for desensitization to cytisine. As in Sprague-Dawley rats, in SHRLJ and WKYLJ rats the cardiovascular and behavioral responses to intrathecal nicotine were significantly inhibited by mecamylamine, dihydro-beta-erthyroidine, and methyllycaconitine. However, methyllycaconitine, which effectively blocked cytisine-elicited cardiovascular and behavioral responses in Sprague-Dawley and WKYLJ rats, was unable to inhibit the maximal rise in cystine-elicited blood pressure, heart rate, and irritation responses in SHRLJ. In contrast to the heightened cardiovascular and behavioral responses, the number of nicotinic binding sites in spinal cord membranes was significantly decreased in the hypertensive rats.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

据报道,中枢胆碱能活性异常在自发性高血压大鼠(SHR)高血压发病机制中起部分作用。在脑和脊髓中给予胆碱能激动剂会导致SHR的升压反应增强。迄今为止的研究主要集中在毒毒胆碱能毒蕈碱系统。最近,我们证明鞘内注射烟碱激动剂会导致升压、心动过速和刺激反应。在本研究中,我们检测了在拉霍亚品系(LJ)SHRLJ和年龄匹配的Wistar-Kyoto(WKYLJ)大鼠中鞘内注射尼古丁和金雀花碱后的心血管和行为反应。与正常血压大鼠相比,烟碱激动剂在SHRLJ中产生增强的升压、心率和刺激反应。在SHRLJ和WKYLJ大鼠中,金雀花碱引起的伤害性反应和升压反应的脊髓延髓成分均比尼古丁更大。SHRLJ和WKYLJ大鼠的不同之处还在于,SHRLJ品系对金雀花碱脱敏的趋势减弱。与Sprague-Dawley大鼠一样,在SHRLJ和WKYLJ大鼠中,美加明、二氢-β-刺桐啶和甲基lycaconitine可显著抑制鞘内注射尼古丁后的心血管和行为反应。然而,甲基lycaconitine虽然能有效阻断Sprague-Dawley和WKYLJ大鼠中由金雀花碱引起的心血管和行为反应,但无法抑制SHRLJ中金雀花碱引起的血压、心率和刺激反应的最大升高。与增强的心血管和行为反应相反,高血压大鼠脊髓膜中烟碱结合位点的数量显著减少。(摘要截短至250字)

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