Heart crosstalk with other organs and pharmacological strategies for cardioprotection

Zizhuo TU, Yaozu XIANG
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Abstract

Cardiovascular disease (CVD) is the leading cause of death worldwide. It has been recognized that specific regulatory factors from peripheral tissues can influence the pathological progression of atherosclerosis, myocardial infarction (MI) and heart failure (HF). Drugs targeting the regulation of pathways related to hepatic lipid metabolism, intestinal flora, renal sodium excretion and hypoglycemia, bone marrow clonal hematopoiesis and immune inflammation, such as Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, Sodium-glucose Cotransporter-2 (SGLT2) inhibitors, IL-1β monoclonal antibodies and Chimeric antigen receptor (CAR) -T therapy, have been shown to have significant protective effects in the prevention and treatment of cardiovascular disease, especially ischemic heart disease and HF. Various forms of interaction between cardiovascular system diseases and cerebrovascular, liver and intestinal metabolism, kidney and other functional disorders have been widely reported. In this review, we focus on the interactions between the cardiovascular system and other organs in ischemic heart disease and HF, highlight novel therapeutic strategies that modulate cardiometabolic and inflammatory processes.

心脏与其他器官的串扰及心脏保护的药理学策略
心血管疾病(CVD)是世界范围内死亡的主要原因。人们已经认识到,来自外周组织的特定调节因子可以影响动脉粥样硬化、心肌梗死(MI)和心力衰竭(HF)的病理进展。靶向调节肝脏脂质代谢、肠道菌群、肾脏钠排泄和低血糖、骨髓克隆造血和免疫炎症相关通路的药物,如枯草素蛋白转化酶9型(PCSK9)抑制剂、钠-葡萄糖共转运蛋白2 (SGLT2)抑制剂、IL-1β单克隆抗体和嵌合抗原受体(CAR) -T治疗;已被证明在预防和治疗心血管疾病,特别是缺血性心脏病和心力衰竭方面具有显著的保护作用。心血管系统疾病与脑血管、肝肠代谢、肾脏等功能障碍之间各种形式的相互作用已被广泛报道。在这篇综述中,我们将重点关注缺血性心脏病和心衰中心血管系统和其他器官之间的相互作用,强调调节心脏代谢和炎症过程的新治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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