首页> 外文期刊>The journal of sexual medicine >High Salt Intake Impairs Erectile Function in Salt-Sensitive Rats Through Mineralocorticoid Receptor Pathway Beyond Its Effect on Blood Pressure
【24h】

High Salt Intake Impairs Erectile Function in Salt-Sensitive Rats Through Mineralocorticoid Receptor Pathway Beyond Its Effect on Blood Pressure

机译:通过超越其对血压影响的矿物质皮质激素受体途径,高盐摄入量损害盐敏感大鼠的勃起功能

获取原文
获取原文并翻译 | 示例
           

摘要

Background: High salt intake is a risk factor for hypertension, which can potentially lead to erectile dysfunction (ED); however, the underlying pathological mechanisms remain unclear. Aim: To investigate whether erectile function is directly impaired by high salt intake and whether selective inhibition of mineralocorticoid receptor (MR) could provide protection from ED. Methods: 6 -week-old male Dahl salt -sensitive rats were randomly divided into 3 groups: normal diet (0.3% NaCl; control, n = 8), high -salt diet (8% NaCl; HS, n = 8), and high -salt diet plus eplerenone (HS + EPL, n = 11). HS + EPL rats were orally administered daily doses of EPL (75 mg/kg) for 6 weeks; control and HS rats received puri fied water on the same schedule. Outcomes: At the end of the study period, erectile function was evaluated by measuring intracavernosal pressure and mean arterial pressure after cavernous nerve stimulation. Serum levels of asymmetric dimethylarginine and L-arginine were determined using ultraperformance liquid chromatography -tandem mass spectrometry. Quantitative PCR was used to assess the expression of MR, in flammation, and oxidative stress markers (nicotinamide adenine dinucleotide phosphate oxidase-1/4, p22(phox) , interleukin-6, and superoxide dismutase-1), and protein arginine N-methyltransferase-1. Results: The intracavernosal pressure/mean arterial pressure ratio was signi ficantly lower, whereas systolic blood pressure, MR expression, serum asymmetric dimethylarginine levels, oxidative stress, and levels of in flammatory biomarkers were signi ficantly higher in HS rats than in control rats ( P < .05). EPL administration signi ficantly improved each of these parameters except systolic blood pressure and MR expression. No signi ficant intergroup differences were observed for L-arginine and superoxide dismutase-1 levels. Clinical Translation: Our results provide a rationale for the need of salt restriction and the use of selective MR inhibitors in prophylaxis or treatment of ED in men consuming a high -salt diet. Strengths & Limitations: We are the first to report that the adverse impact of high salt intake on erectile function is mediated via MR activation, independent of its effect on blood pressure. A major limitation of this study is that responses of salt -resistant rats were not studied. Conclusions: High salt intake directly impaired erectile function in Dahl salt -sensitive rats, whereas selective MR inhibition ameliorated this effect. Kishimoto T, Kataoka T, Yamamoto Y, et al. High Salt Intake Impairs Erectile Function in Salt -Sensitive Rats Through Mineralocorticoid Receptor Pathway Beyond Its Effect on Blood Pressure. J Sex Med 2020;17:1280 - 1287.
机译:背景:高盐摄入是高血压的危险因素,可能导致勃起功能障碍(ED);然而,潜在的病理机制仍不清楚。目的:探讨高盐摄入是否会直接损害勃起功能,选择性抑制盐皮质激素受体(MR)是否能保护ED。方法:6周龄雄性达尔盐敏感大鼠随机分为3组:正常饮食(0.3%NaCl;对照组,n=8)、高盐饮食(8%NaCl;HS,n=8),高盐饮食加依普利酮(HS+EPL,n=11)。HS+EPL大鼠口服每日剂量的EPL(75mg/kg),持续6周;对照组和HS大鼠按照相同的时间表接受纯化水。结果:在研究结束时,通过测量海绵体内压和海绵体神经刺激后的平均动脉压来评估勃起功能。采用超高效液相色谱-串联质谱法测定不对称二甲基精氨酸和L-精氨酸的血清水平。定量PCR用于评估MR、炎症和氧化应激标记物(烟酰胺腺嘌呤二核苷酸磷酸氧化酶-1/4、p22(phox)、白细胞介素-6和超氧化物歧化酶-1)和蛋白精氨酸N-甲基转移酶-1的表达。结果:HS大鼠的海绵体内压/平均动脉压比值显著低于对照组大鼠,而收缩压、MR表达、血清不对称二甲基精氨酸水平、氧化应激和炎症生物标志物水平显著高于对照组大鼠(P<0.05)。EPL给药显著改善了除收缩压和MR表达外的所有这些参数。未观察到L-精氨酸和超氧化物歧化酶-1水平的组间差异。临床翻译:我们的研究结果为食用高盐饮食的男性在预防或治疗ED时需要限制盐和使用选择性MR抑制剂提供了理论依据。优点和局限性:我们是第一个报道高盐摄入对勃起功能的不利影响是通过MR激活介导的,与血压的影响无关。这项研究的一个主要限制是没有研究耐盐大鼠的反应。结论:高盐摄入直接损害了Dahl盐敏感大鼠的勃起功能,而选择性MR抑制改善了这种影响。Kishimoto T,Kataoka T,Yamamoto Y等。高盐摄入通过盐皮质激素受体途径损害盐敏感大鼠的勃起功能,而不仅仅是其对血压的影响。J Sex Med 2020;17:1280 - 1287.

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号