ENDOGENOUS OPIOIDS, PAIN AND BLOOD PRESSURE CONTROL

内源性阿片类药物、疼痛和血压控制

• 批准号: 6183160
• 负责人: JAMES A MCCUBBIN
• 金额: $ 20.71万
• 依托单位: CLEMSON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1989
• 资助国家: 美国
• 起止时间: 1989-08-01 至 2003-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6183160
• 关键词: analgesia; behavior test; blood chemistry; blood pressure; clinical research; disease /disorder proneness /risk; endogenous opioid; essential hypertension; gender difference; hormone regulation /control mechanism; human subject; naltrexone; neuroendocrine system; opioid receptor; pain; stress

This proposal is for continuation of our ongoing research on opioid abnormalities and blood pressure reactivity in persons at risk for hypertension. We are gradually becoming aware that regulation of both blood pressure and pain sensitivity is altered in pre-hypertensive populations. For example, persons at risk for hypertension have decreased opioid inhibition of blood pressure responses to stress. Paradoxically, they also show antinociceptive effects consistent with exaggerated opioid function. The scientific meaningfulness, both basic and clinical, of the links between pain sensitivity alterations and blood pressure dysregulation remains to be clarified. Recent studies by ourselves and others have emphasized the importance of opioids in regulation of 1) neuroendocrine and blood pressure responses to stress in hypertension development, 2) behavioral responses to pain, and 3) the relationship between pain sensitivity and blood pressure. The purpose of this continuation proposal is to further examine the role of endogenous opioids in blood pressure dysregulation by studies of circulatory and behavioral responses to aversive stimuli in persons at enhanced risk for hypertension. This will be accomplished by comparison of the effects of opioid blockade with naltrexone on pain sensitivity and blood pressure reactivity in young men and women with mildly elevated casual blood pressure. We hypothesize that abnormalities of both blood pressure control and pain sensitivity in the early stages of hypertension development are linked to altered opioid peptide function. Persons at risk for hypertension will show exaggerated opioid inhibition of pain sensitivity in the face of diminished opioid inhibition of blood pressure reactivity. Improved understanding of the opioidergic basis of altered pain sensitivity and blood pressure control will clarify the poorly characterized etiology of essential hypertension and possibly offer new preventive, diagnostic and therapeutic strategies.

这项建议是为了继续我们正在进行的研究阿片类药物异常和血压反应性的人在高血压的风险。 我们逐渐意识到，在高血压前期人群中，血压和疼痛敏感性的调节都发生了改变。 例如，有高血压风险的人对压力的血压反应的阿片样物质抑制减少。 巧合的是，它们也显示出与夸大的阿片功能一致的抗伤害作用。 疼痛敏感性改变和血压失调之间的联系在基础和临床上的科学意义仍有待澄清。 我们和其他人最近的研究强调了阿片类药物在调节1）神经内分泌和血压对高血压发展中压力的反应，2）对疼痛的行为反应，以及3）疼痛敏感性和血压之间的关系中的重要性。 本延续提案的目的是通过研究高血压风险增加人群对厌恶刺激的循环和行为反应，进一步研究内源性阿片类药物在血压失调中的作用。 这将通过比较阿片类药物阻滞与纳洛酮对偶尔血压轻度升高的年轻男性和女性的疼痛敏感性和血压反应性的影响来实现。 我们推测，在高血压发展的早期阶段，血压控制和疼痛敏感性的异常与阿片肽功能的改变有关。 有高血压风险的人在阿片类药物对血压反应性的抑制减弱的情况下，会表现出阿片类药物对疼痛敏感性的过度抑制。 对改变疼痛敏感性和血压控制的阿片能基础的进一步理解将澄清原发性高血压的病因学，并可能提供新的预防，诊断和治疗策略。