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Functional cardiovascular action of L-cysteine microinjected into pressor sites of the rostral ventrolateral medulla of the rat

机译:将L-半胱氨酸微注射到大鼠喙侧腹外侧延髓的加压部位中的功能性心血管作用

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The endogenous sulfur-containing amino acid L-cysteine injected into the cerebrospinal fluid space of the cisterna magna increases arterial blood pressure (ABP) and heart rate (HR) in the freely moving rat. The present study examined (1) cardiovascular responses to L-cysteine microinjected into the rostral ventrolateral medulla (RVLM), where a group of neurons regulate activities of cardiovascular sympathetic neurons and (2) involvement of ionotropic excitatory amino acid (iEAA) receptors in response. In the RVLM of urethane-anesthetized rats accessed ventrally and identified with pressor responses to L-glutamate (10 mM, 34 nl), microinjections of L-cysteine increased ABP and HR dose dependently (3-100 mM, 34 nl). The cardiovascular responses to L-cysteine (30 mM) were not attenuated by a prior injection of either antagonist alone, MK801 (20 mM, 68 nl) for the NMDA type of iEAA receptors, or CNQX (2 mM) for the non-NMDA type. However, inhibition of both NMDA and non-NMDA receptors with additional prior injection of either antagonist completely blocked those responses to L-cysteine. The results indicate that L-cysteine has functional cardiovascular action in the RVLM of the anesthetized rat, and the responses to L-cysteine involve both NMDA and non-NMDA receptors albeit in a mutually exclusive parallel fashion. The findings may suggest endogenous roles of L-cysteine indirectly via iEAA receptors in the neuronal network of the RVLM for cardiovascular regulation in physiological and pathological situations.
机译:注入大水罐的脑脊髓液空间的内源性含硫氨基酸L-半胱氨酸会增加自由移动大鼠的动脉血压(ABP)和心率(HR)。本研究研究了(1)显微注射入延髓腹侧延髓(RVLM)的L-半胱氨酸的心血管反应,其中一组神经元调节心血管交感神经元的活动,以及(2)离子型兴奋性氨基酸(iEAA)受体参与反应。在经尿烷麻醉的大鼠的RVLM中,经腹腔进入的大鼠具有对L-谷氨酸的升压反应(10 mM,34 nl),微量注射L-半胱氨酸可增加ABP和HR剂量(3-100 mM,34 nl)。事先注射任何一种拮抗剂,NMDA型iEAA受体的MK801(20 mM,68 nl)或非NMDA的CNQX(2 mM)都不会减弱对L-半胱氨酸(30 mM)的心血管反应。类型。但是,在事先注射任何一种拮抗剂的情况下,抑制NMDA和非NMDA受体完全抑制了对L-半胱氨酸的反应。结果表明,L-半胱氨酸在麻醉大鼠的RVLM中具有心血管功能,并且对L-半胱氨酸的反应涉及NMDA和非NMDA受体,尽管它们是相互排斥的平行方式。这些发现可能暗示L-半胱氨酸通过iEAA受体在RVLM神经元网络中间接作用于内在作用,以在生理和病理情况下进行心血管调节。

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