Department of Physiology and Biophysics, Mississippi Center for Obesity Research, Cardiorenal and Metabolic Diseases Research Center, University of Mississippi Medical Center, Jackson, Mississippi, United States.
Centro Universitário Barão de Mauá, Ribeirao Preto, Brazil.
Am J Physiol Regul Integr Comp Physiol. 2023 Oct 1;325(4):R401-R410. doi: 10.1152/ajpregu.00106.2023. Epub 2023 Jul 31.
We examined potential sex differences in appetite and blood pressure (BP) responses to melanocortin-4 receptor (MC4R) blockade in offspring from lean and obese parents. Offspring from normal (N) diet-fed parents were fed N (NN) or high-fat (H) diets (NH) from weaning until adulthood. Offspring from obese H diet-fed parents were also fed N (HN) or H diets (HH). Adult male and female offspring were implanted with BP telemetry probes and intracerebroventricular cannulas to infuse MC4R antagonist or vehicle. Infusion of the MC4R antagonist SHU-9119 (1 nmol/h) for 7 days caused larger increases in calorie intake and body weight in obese compared with lean offspring. In male offspring, HH and HN groups exhibited higher baseline BP compared with NN and NH, and HH showed a greater reduction in BP during SHU-9119 infusion. In female offspring, HH also showed higher baseline BP and greater reduction in BP during MC4R blockade. SHU-9119 reduced heart rate in all groups, but reductions were more pronounced in offspring from lean parents. Combined α and β-adrenergic blockade reduced BP more in male HH offspring compared with NN controls. Losartan reduced BP more in male NH, HN, and HH offspring compared with NN controls. Losartan and α- and β-adrenergic blockade reduced BP similarly in all female groups. These results suggest that endogenous MC4R activity contributes to elevated BP in obese offspring from obese parents. Our findings also indicate important sex differences in the mechanisms of BP control in male and female offspring of obese parents.
我们研究了瘦素和肥胖父母后代对黑皮质素-4 受体(MC4R)阻断剂的食欲和血压(BP)反应的潜在性别差异。来自正常饮食喂养父母的后代在断奶后至成年期间分别喂食正常饮食(NN)或高脂肪饮食(NH)。来自肥胖高脂肪饮食喂养父母的后代也喂食正常饮食(HN)或高脂肪饮食(HH)。成年雄性和雌性后代植入 BP 遥测探头和脑室内套管以输注 MC4R 拮抗剂或载体。连续 7 天输注 MC4R 拮抗剂 SHU-9119(1 nmol/h)导致肥胖后代的热量摄入和体重增加明显大于瘦素后代。在雄性后代中,HH 和 HN 组的基础血压高于 NN 和 NH 组,并且在 SHU-9119 输注期间,HH 组的血压降低幅度更大。在雌性后代中,HH 组也表现出更高的基础血压和 MC4R 阻断期间血压降低幅度更大。SHU-9119 降低了所有组的心率,但在瘦素父母的后代中降低更为明显。联合α和β肾上腺素能阻断在雄性 HH 后代中降低 BP 的效果比 NN 对照组更为显著。氯沙坦在雄性 NH、HN 和 HH 后代中降低 BP 的效果比 NN 对照组更为显著。氯沙坦和α和β肾上腺素能阻断在所有雌性组中降低 BP 的效果相似。这些结果表明,内源性 MC4R 活性导致肥胖父母肥胖后代的 BP 升高。我们的研究结果还表明,肥胖父母的雄性和雌性后代的 BP 控制机制存在重要的性别差异。