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外周 δ-阿片受体可减弱运动性血压反射。

Peripheral δ-opioid receptors attenuate the exercise pressor reflex.

机构信息

Heart and Vascular Institute, Penn State College of Medicine, Hershey, Pennsylvania; and.

出版信息

Am J Physiol Heart Circ Physiol. 2013 Oct 15;305(8):H1246-55. doi: 10.1152/ajpheart.00116.2013. Epub 2013 Aug 9.

Abstract

In rats with ligated femoral arteries, the exercise pressor reflex is exaggerated, an effect that is attenuated by stimulation of peripheral μ-opioid receptors on group IV metabosensitive afferents. In contrast, δ-opioid receptors are expressed mostly on group III mechanosensitive afferents, a finding that prompted us to determine whether stimulation of these opioid receptors could also attenuate the exaggerated exercise pressor reflex in "ligated" rats. We found femoral arterial injection of [D-Pen2,D-Pen5]enkephalin (DPDPE; 1.0 μg), a δ-opioid agonist, significantly attenuated the pressor and cardioaccelerator components of the exercise pressor reflex evoked by hindlimb muscle contraction in both rats with ligated and patent femoral arteries. DPDPE significantly decreased the pressor responses to muscle mechanoreflex activation, evoked by tendon stretch, in ligated rats only. DPDPE (1.0 μg) had no effect in either group on the pressor and cardioaccelerator responses to capsaicin (0.2 μg), which primarily stimulates group IV afferents. DPDPE (1.0 μg) had no effect on the pressor and cardioaccelerator responses to lactic acid (24 mM), which stimulates group III and IV afferents, in rats with patent femoral arteries but significantly decreased the pressor response in ligated rats. Western blots revealed the amount of protein comprising the δ-opioid receptor was greater in dorsal root ganglia innervating hindlimbs with ligated femoral arteries than in dorsal root ganglia innervating hindlimbs with patent femoral arteries. Our findings support the hypothesis that stimulation of δ-opioid receptors on group III afferents attenuated the exercise pressor reflex.

摘要

在结扎股动脉的大鼠中,运动升压反射被夸大,这种效应可被刺激 IV 组代谢敏感性传入纤维上的外周 μ 阿片受体所减弱。相比之下,δ 阿片受体主要表达在 III 组机械敏感性传入纤维上,这一发现促使我们确定刺激这些阿片受体是否也能减弱“结扎”大鼠中过度的运动升压反射。我们发现,股动脉内注射[D-Pen2,D-Pen5]脑啡肽(DPDPE;1.0μg),一种 δ 阿片受体激动剂,可显著减弱结扎和未结扎股动脉大鼠后肢肌肉收缩引起的升压和心加速反射的升压和心加速成分。DPDPE 显著降低了仅在结扎大鼠中由肌腱拉伸引起的肌肉机械反射激活的升压反应。在两组大鼠中,DPDPE(1.0μg)对辣椒素(0.2μg)引起的升压和心加速反应均无影响,辣椒素主要刺激 IV 组传入纤维。DPDPE(1.0μg)对未结扎股动脉大鼠中乳酸(24mM)引起的升压和心加速反应均无影响,但可显著降低结扎股动脉大鼠的升压反应。Western blot 显示,支配结扎股动脉后肢的背根神经节中包含 δ 阿片受体的蛋白量大于支配未结扎股动脉后肢的背根神经节。我们的发现支持这样的假设,即刺激 III 组传入纤维上的 δ 阿片受体可减弱运动升压反射。

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