首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >In vivo expression of ganglionic long-term potentiation in superior cervical ganglia from hypertensive aged rats.
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In vivo expression of ganglionic long-term potentiation in superior cervical ganglia from hypertensive aged rats.

机译:高血压老年大鼠上颈神经节中神经节长时程增强的体内表达。

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摘要

Sustained increase in central sympathetic outflow to ganglia may provide the repeated high frequency presynaptic activity required for induction of long-term potentiation in sympathetic ganglia (gLTP), which is known to be involved in the manifestation of a neurogenic form of hypertension, namely stress-hypertension. Aging is often viewed as a progressive decline in physiological competence with a corresponding impaired ability to adapt to stressful stimuli. Old animals have exaggerated sympathetic activity as well as increased morbidity and mortality during prolonged exposure to stressful stimuli. Using the superior cervical ganglion (SCG) as a model for sympathetic ganglia, electrophysiological and biochemical evidence show that mildly hypertensive aged rats (22-month old) have expressed gLTP in vivo. This is suggested by a number of lines of evidence. Firstly, a shift in input/output (I/O) curve of ganglia from aged rats to the left side of I/O curve of ganglia from 6-month old (adult) rats indicating expression of gLTP. Secondly, failure of in vitro high frequency stimulation to induce gLTP in ganglia isolated from aged rats, which indicates occlusion due to saturation, which, in turn, suggests in vivo expression of gLTP in these ganglia. Thirdly, in vitro inhibition of basal ganglionic transmission by blockers of gLTP (5-HT(3) antagonists) is observed in ganglia isolated from aged rats, but not in those from adult rats. Finally, immunoblot analysis revealed that protein levels of signaling molecules such as calcium-calmodulin kinase II (CaMKII; phosphorylated and total), which normally increase during expression of LTP, are elevated in ganglia isolated from aged rats compared to those from adult ones. Protein levels of calcineurin, which dephosphorylates P-CaMKII, were reduced in ganglia isolated from aged rats, probably as a support mechanism to allow prolonged phosphorylation of CaMKII. Our findings suggest in vivo expression of gLTP in sympathetic ganglia of aged animals, which may contribute to the moderate hypertension often seen in aged subjects.
机译:中央交感神经向神经节外流的持续增加可能会提供诱导交感神经节(gLTP)长期增强所需的反复的高频突触前活动,已知这与高血压的神经源性形式的表现有关,即压力-高血压。衰老通常被认为是生理能力的逐步下降,其适应压力刺激的能力相应减弱。在长时间暴露于压力刺激下,老动物具有夸大的交感神经活动以及发病率和死亡率增加。使用上颈神经节(SCG)作为交感神经节的模型,电生理和生化证据表明,轻度高血压的老年大鼠(22个月大)已在体内表达了gLTP。许多证据表明了这一点。首先,老年大鼠神经节的输入/输出(I / O)曲线向6月龄(成年)大鼠神经节的I / O曲线的左侧偏移,表明gLTP的表达。其次,体外高频刺激未能诱导从衰老大鼠中分离出的神经节中的gLTP,这表明由于饱和引起的闭塞,这又暗示了gLTP在这些神经节中的体内表达。第三,在从老年大鼠中分离出的神经节中观察到了由gLTP阻断剂(5-HT(3)拮抗剂)对基础神经节传递的抑制作用,而在成年大鼠中则没有。最后,免疫印迹分析表明,从成年大鼠中分离出的神经节中,成年大鼠的神经节中的信号分子如钙钙调蛋白激酶II(CaMKII;磷酸化和总蛋白)的蛋白质水平通常在LTP表达过程中增加。钙调神经磷酸酶的蛋白水平会降低P-CaMKII的磷酸水平,而该蛋白从衰老大鼠的神经节中降低,这可能是支持其延长CaMKII磷酸化的一种支持机制。我们的发现表明,gLTP在衰老动物交感神经节中体内表达,这可能有助于在老年受试者中常见的中度高血压。

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