Hill-Pryor Crystal, Lindsey DaShawnda, Lapanowski Karen, Dunbar Joseph C
Wayne State University School of Medicine, Department of Physiology, 5374 Scott Hall, 540 E. Canfield, Detroit, MI 48201-1928, USA.
Peptides. 2006 Jun;27(6):1520-6. doi: 10.1016/j.peptides.2005.10.012. Epub 2005 Nov 15.
Beta-endorphin decreases blood pressure in normal rats but increases blood pressure in obese rats. Since beta-endorphins can bind both mu opioid and kappa-opioid receptors we investigated the effect of a mu specific receptor agonist, D-Ala2,N-Me-Phe4,Gly5-ol]-enkephalin (DAMGO) and a mu specific antagonist, D-Phe-Cys-Trp-Arg-Thr-Pen-Thr-NH2 (CTAP) on cardiovascular responses in conscious control and obese rats. Rats were also implanted with telemetry transmitters and intracerebroventricular (ICV) cannulas for recording and peptide administration. The mu agonist, DAMGO, increased blood pressure (BP) in control rats. DAMGO also increased BP in obese rats but only at high concentrations. The heart rate responses paralleled the MAP responses. CTAP, the mu antagonist, paradoxically increased the MAP in both control and obese rats. The responsiveness to the mu agonist and antagonist was greater in controls. In other animals the brains were excised and the ventral medial hypothalamic area removed and mu receptor expression determined using PCR. The expression of mu opioid receptors was increased in obese rats. We conclude that the mu opioids can stimulate cardiovascular responses, but the excitatory responsiveness was not increased in conscious obese rats.
β-内啡肽可降低正常大鼠的血压,但会升高肥胖大鼠的血压。由于β-内啡肽能与μ阿片受体和κ阿片受体结合,我们研究了μ特异性受体激动剂[D-Ala2,N-Me-Phe4,Gly5-ol]-脑啡肽(DAMGO)和μ特异性拮抗剂D-Phe-Cys-Trp-Arg-Thr-Pen-Thr-NH2(CTAP)对清醒对照大鼠和肥胖大鼠心血管反应的影响。大鼠还植入了遥测发射器和脑室内(ICV)插管,用于记录和肽给药。μ激动剂DAMGO可使对照大鼠的血压升高。DAMGO也可使肥胖大鼠的血压升高,但仅在高浓度时。心率反应与平均动脉压反应平行。μ拮抗剂CTAP反常地使对照大鼠和肥胖大鼠的平均动脉压升高。对照大鼠对μ激动剂和拮抗剂的反应性更高。在其他动物中,切除大脑并去除腹内侧下丘脑区域,使用聚合酶链反应(PCR)测定μ受体表达。肥胖大鼠中μ阿片受体的表达增加。我们得出结论,μ阿片类药物可刺激心血管反应,但清醒肥胖大鼠的兴奋性反应性并未增加。