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在代谢综合征猪模型中,SGLT-2抑制剂卡格列净对心肌功能和血管生成的性别特异性改善

Sex-Specific Improvements in Myocardial Function and Angiogenesis with SGLT-2 Inhibitor Canagliflozin in a Swine Model of Metabolic Syndrome.

作者信息

Harris Dwight D, Broadwin Mark, Stone Christopher, Sabe Sharif A, Kanuparthy Meghamsh, Nho Ju-Woo, Muir Kelsey C, Abid M Ruhul, Sellke Frank W

机构信息

Division of Cardiothoracic Surgery, Department of Surgery, Cardiovascular Research Center, Alpert Medical School of Brown University, Brown University Health, 2 Dudley Street, MOC 360, Providence, RI 02905, USA.

出版信息

Int J Mol Sci. 2025 Feb 22;26(5):1887. doi: 10.3390/ijms26051887.

Abstract

There is a significant body of literature to suggest that coronary artery disease (CAD) is a highly sex-specific disease. The study of sex-specific therapeutics and sex-specific responses to treatment for CAD remains underreported in the literature. Sodium-glucose transporter 2 (SGLT2) inhibitors are of growing interest in the treatment of ischemic heart disease and heart failure; however, the sex-specific response to SGLT2 inhibitors is unknown. We studied an SGLT2 inhibitor, canagliflozin, in a swine model of metabolic syndrome (MS) and chronic myocardial ischemia with emphasis on the sex-specific outcomes. Yorkshire swine ( = 21) were obtained at 6 weeks of age and fed a high-fat diet to induce MS. Left thoracotomy was performed on all swine at 11 weeks of age for the placement of an ameroid constrictor to model chronic myocardial ischemia. Swine recovered for two weeks, then were assigned to either the drug group, CAN 300 mg daily group (M = 5, F = 5), or the control group (CON, M = 5, F = 6). Both groups received 5 weeks of therapy. After completion of therapy, swine underwent functional assessment and terminal harvest. The male animals treated with CAN (CAN-M) had significant increases in stroke volume and cardiac output ( = 0.047, < 0.001) compared to control males (CON-M), which were not seen in females treated with CAN (CAN-F) compared to control females (CON-F). Effective arterial elastance was decreased in CAN-M compared to CON-M. The CAN-F group had a significant increase in ischemic myocardial capillary density compared to CON-F ( = 0.04). There was no difference in capillary density between the CAN-M and CON-M groups. CAN treatment resulted in sex-specific changes in angiogenesis and myocardial function. The CAN-M group had significant improvements in cardiac function based on afterload reduction, stroke volume, and increased cardiac output not seen in the CAN-F group. The CAN-F group had increased ischemic myocardial capillary density. These findings provide a foundation for further investigation of the sex-specific effects of SGLT-2 inhibitors in humans.

摘要

有大量文献表明冠状动脉疾病(CAD)是一种高度性别特异性的疾病。关于CAD的性别特异性治疗方法以及对治疗的性别特异性反应的研究在文献中报道较少。钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂在缺血性心脏病和心力衰竭的治疗中越来越受到关注;然而,SGLT2抑制剂的性别特异性反应尚不清楚。我们在代谢综合征(MS)和慢性心肌缺血的猪模型中研究了一种SGLT2抑制剂卡格列净,重点关注性别特异性结果。在6周龄时获得约克夏猪(n = 21),并给予高脂饮食以诱导MS。在11周龄时对所有猪进行左胸切开术,放置阿梅里德缩窄环以模拟慢性心肌缺血。猪恢复两周后,被分配到药物组,即每日300毫克卡格列净组(雄性 = 5只,雌性 = 5只),或对照组(CON,雄性 = 5只,雌性 = 6只)。两组均接受5周的治疗。治疗结束后,对猪进行功能评估并进行终末取材。与对照雄性猪(CON-M)相比,接受卡格列净治疗的雄性动物(CAN-M)的每搏输出量和心输出量显著增加(P = 0.047,P < 0.001),而与对照雌性猪(CON-F)相比,接受卡格列净治疗的雌性动物(CAN-F)未出现这种情况。与CON-M相比,CAN-M的有效动脉弹性降低。与CON-F相比,CAN-F组的缺血心肌毛细血管密度显著增加(P = 0.04)。CAN-M组和CON-M组之间的毛细血管密度没有差异。卡格列净治疗导致血管生成和心肌功能出现性别特异性变化。基于后负荷降低、每搏输出量增加和心输出量增加,CAN-M组的心脏功能有显著改善,而CAN-F组未出现这种情况。CAN-F组的缺血心肌毛细血管密度增加。这些发现为进一步研究SGLT-2抑制剂在人类中的性别特异性作用提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c488/11900068/b17eb8be8961/ijms-26-01887-g002.jpg

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