Key Laboratory of Cardiovascular Disease and Molecular Intervention, Department of Physiology, Nanjing Medical University, Nanjing 210029, China.
Exp Physiol. 2013 Feb;98(2):435-43. doi: 10.1113/expphysiol.2012.067256. Epub 2012 Aug 7.
Central melanocortin 3/4 receptors (MC3/4Rs) are known to regulate energy balance. Activation of MC3/4Rs causes a greater increase in the firing activity of the PVN neurons in obese Zucker rats than in lean Zucker rats. The present study was undertaken to determine the roles of MC3/4Rs in the hypothalamic paraventricular nucleus (PVN) in modulating the sympathetic activity and blood pressure and its downstream pathway. Renal sympathetic nerve activity (RSNA) and mean arterial pressure (MAP) were recorded in anaesthetized rats. Microinjection of the MC3/4R agonist melanotan II (MTII) into the PVN increased the RSNA and MAP. The MC3/4R antagonist agouti-related peptide (AgRP) or SHU9119 decreased the RSNA and MAP, but the MC4R antagonist HS024 had no significant effect on the RSNA and MAP. The effects of MTII were abolished by pretreatment of the PVN with AgRP, SHU9119, the adenylate cyclase inhibitor SQ22536 or the protein kinase A inhibitor Rp-cAMP, and substantially attenuated by HS024. Microinjection of SQ22536 alone into the PVN had no significant effect on the RSNA and MAP, but Rp-cAMP caused significant decreases in the RSNA and MAP. Furthermore, MTII increased the cAMP level in the PVN. These results indicate that activation of MC3/4Rs in the PVN increases the sympathetic outflow and blood pressure via the cAMP-protein kinase A pathway. Melanocortin 3 receptors in the PVN may exert a tonic excitatory effect on sympathetic activity.
中央黑色素皮质素 3/4 受体(MC3/4Rs)已知可调节能量平衡。MC3/4Rs 的激活会导致肥胖 Zucker 大鼠的 PVN 神经元的放电活动比瘦 Zucker 大鼠更大幅度的增加。本研究旨在确定 MC3/4Rs 在调节交感神经活性和血压及其下游途径中的下丘脑室旁核(PVN)中的作用。在麻醉大鼠中记录肾交感神经活动(RSNA)和平均动脉压(MAP)。将 MC3/4R 激动剂黑色素促黑激素 II(MTII)微注射到 PVN 中会增加 RSNA 和 MAP。MC3/4R 拮抗剂 agouti 相关肽(AgRP)或 SHU9119 降低了 RSNA 和 MAP,但 MC4R 拮抗剂 HS024 对 RSNA 和 MAP 没有明显影响。PVN 中 AgRP、SHU9119、腺苷酸环化酶抑制剂 SQ22536 或蛋白激酶 A 抑制剂 Rp-cAMP 的预处理可消除 MTII 的作用,而 HS024 则大大减弱了其作用。单独将 SQ22536 微注射到 PVN 中对 RSNA 和 MAP 没有明显影响,但 Rp-cAMP 导致 RSNA 和 MAP 显著下降。此外,MTII 增加了 PVN 中的 cAMP 水平。这些结果表明,PVN 中 MC3/4Rs 的激活通过 cAMP-蛋白激酶 A 途径增加交感神经输出和血压。PVN 中的黑色素皮质素 3 受体可能对交感神经活动产生紧张的兴奋作用。