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Inhibition of the ERK pathway prevents HIVgp120-induced REM sleep increase.

机译:抑制ERK通路可防止HIVgp120诱导的REM睡眠增加。

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摘要

Approximately 35% of HIV-infected subjects, both children and adults, exhibit alterations in the sleep-waking cycle. HIV surface glycoprotein gp120 has been postulated to contribute to this abnormality. For example, it has been reported that HIVgp120 modifies sleep in freely-moving rats and that it also activates the ERK pathway in brain slices. The goal of this work was to determine if sleep changes induced by HIVgp120 in normal rats are mediated by the MAPK pathway. Our results show that a single intraventricular administration of HIVgp120 selectively increases REMS and that such an increase can be prevented by U0126, an inhibitor of ERK activating enzyme, MEK. In contrast, SB202190, a MAPK-p38 inhibitor, had no effect on HIVgp120-induced increase in REMS. These results suggest that HIVgp120 increases REMS in the rat by specifically affecting the ERK signal transduction pathway.
机译:无论是儿童还是成人,大约35%的HIV感染者的睡眠觉醒周期都有变化。推测HIV表面糖蛋白gp120会导致这种异常。例如,据报道,HIVgp120改变了自由运动大鼠的睡眠,并且还激活了脑切片中的ERK途径。这项工作的目的是确定在正常大鼠中,HIVgp120诱导的睡眠变化是否由MAPK途径介导。我们的结果表明,单次脑室内给予HIVgp120有选择地增加REMS,而ERK活化酶抑制剂MEK U0126可以阻止这种增加。相反,MAPK-p38抑制剂SB202190对HIVgp120诱导的REMS升高没有影响。这些结果表明,HIVgp120通过特异性地影响ERK信号转导途径而增加了大鼠的REMS。

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