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首页> 外文期刊>Hypertension: An Official Journal of the American Heart Association >Leptin acts in the forebrain to differentially influence baroreflex control of lumbar, renal, and splanchnic sympathetic nerve activity and heart rate
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Leptin acts in the forebrain to differentially influence baroreflex control of lumbar, renal, and splanchnic sympathetic nerve activity and heart rate

机译:瘦素在前脑中发挥作用,以不同方式影响腰,肾和内脏交感神经活动和心率的压力反射控制

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Although leptin is known to increase sympathetic nerve activity (SNA), we tested the hypothesis that leptin also enhances baroreflex control of SNA and heart rate (HR). Using α-chloralose anesthetized male rats, mean arterial pressure (MAP), HR, lumbar SNA (LSNA), splanchnic SNA (SSNA), and renal SNA (RSNA) were recorded before and for 2 hours after lateral cerebroventricular leptin or artificial cerebrospinal fluid administration. Baroreflex function was assessed using a 4-parameter sigmoidal fit of HR and SNA responses to slow ramp (3-5 minutes) changes in MAP, induced by intravenous infusion of nitroprusside and phenylephrine. Leptin (3 μg) increased (P<0.05) basal LSNA, SSNA, RSNA, HR, and MAP, and the LSNA, SSNA, RSNA, and HR baroreflex maxima. Leptin also increased gain of baroreflex control of LSNA and RSNA, but not of SSNA or HR. The elevations in HR were eliminated by pretreatment with methscopalamine, to block parasympathetic nerve activity; however, after cardiac sympathetic blockade with atenolol, leptin still increased basal HR and MAP and the HR baroreflex maximum and minimum. Leptin (1.5 μg) also increased LSNA and enhanced LSNA baroreflex gain and maximum, but did not alter MAP, HR, or the HR baroreflex. Lateral cerebroventricular artificial cerebrospinal fluid had no effects. Finally, to test whether leptin acts in the brain stem, leptin (3 μg) was infused into the 4th ventricle; however, no significant changes were observed. In conclusion, leptin acts in the forebrain to differentially influence baroreflex control of LSNA, RSNA, SSNA, and HR, with the latter action mediated via suppression of parasympathetic nerve activity.
机译:尽管已知瘦素可增加交感神经活动(SNA),但我们测试了以下假设:瘦素还可增强SNA和心率(HR)的压力反射控制。使用α-氯藻糖麻醉的雄性大鼠,在侧脑室瘦素或人工脑脊液之前和之后2小时记录平均动脉压(MAP),HR,腰椎SNA(LSNA),内脏SNA(SSNA)和肾SNA(RSNA)。行政。压力反射功能使用HR和SNA对MAP缓慢倾斜(3-5分钟)变化的HR和SNA响应的4参数S形拟合进行评估,该变化由静脉输注硝普钠和去氧肾上腺素引起。瘦素(3μg)增加(P <0.05)基础LSNA,SSNA,RSNA,HR和MAP,以及LSNA,SSNA,RSNA和HR压力反射最大值。瘦素还增加了LSNA和RSNA的压力反射控制的增益,但没有增加SSNA或HR的压力反射控制。通过用甲基倍他命胺预处理可消除HR升高,从而阻止副交感神经活动。然而,在用阿替洛尔心脏交感神经阻滞后,瘦素仍会增加基础HR和MAP以及HR压力反射最大值和最小值。瘦素(1.5μg)还能增加LSNA并增强LSNA压力反射的增益和最大值,但不会改变MAP,HR或HR压力反射。侧脑室人工脑脊液无影响。最后,为了检测瘦素是否在脑干中起作用,将瘦素(3μg)注入第四个脑室。但是,没有观察到明显的变化。总之,瘦素在前脑中发挥作用,以不同方式影响LSNA,RSNA,SSNA和HR的压力反射控制,而后者的作用是通过抑制副交感神经活动介导的。

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