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在体外细胞模型中,盐皮质激素受体拮抗剂的临床特性和非临床测试。

Clinical Properties and Non-Clinical Testing of Mineralocorticoid Receptor Antagonists in In Vitro Cell Models.

机构信息

Department of Dialysis, Clinic for Internal Medicine, University Medical Centre Maribor, Ljubljanska ulica 5, 2000 Maribor, Slovenia.

Department of Pharmacology, Faculty of Medicine, University of Maribor, Taborska ulica 5, 2000 Maribor, Slovenia.

出版信息

Int J Mol Sci. 2024 Aug 22;25(16):9088. doi: 10.3390/ijms25169088.

Abstract

Mineralocorticoid receptor antagonists (MRAs) are one of the renin-angiotensin-aldosterone system inhibitors widely used in clinical practice. While spironolactone and eplerenone have a long-standing profile in clinical medicine, finerenone is a novel agent within the MRA class. It has a higher specificity for mineralocorticoid receptors, eliciting less pronounced adverse effects. Although approved for clinical use in patients with chronic kidney disease and heart failure, intensive non-clinical research aims to further elucidate its mechanism of action, including dose-related selectivity. Within the field, animal models remain the gold standard for non-clinical testing of drug pharmacological and toxicological properties. Their role, however, has been challenged by recent advances in in vitro models, mainly through sophisticated analytical tools and developments in data analysis. Currently, in vitro models are gaining momentum as possible platforms for advanced pharmacological and pathophysiological studies. This article focuses on past, current, and possibly future in vitro cell models research with clinically relevant MRAs.

摘要

醛固酮受体拮抗剂 (MRA) 是临床广泛应用的肾素-血管紧张素-醛固酮系统抑制剂之一。螺内酯和依普利酮在临床医学中已有悠久的应用历史,而非奈利酮则是 MRA 类药物中的一种新型药物。它对醛固酮受体具有更高的特异性,引起的不良反应不那么明显。虽然已批准用于慢性肾脏病和心力衰竭患者,但非临床研究的重点是进一步阐明其作用机制,包括剂量相关的选择性。在该领域,动物模型仍然是药物药代动力学和毒理学性质非临床测试的金标准。然而,最近体外模型的进展对其提出了挑战,主要是通过复杂的分析工具和数据分析的发展。目前,体外模型作为先进的药理学和病理生理学研究的可能平台正在兴起。本文重点介绍了过去、现在和未来可能的临床相关 MRA 的体外细胞模型研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c441/11354261/3237d2bce60f/ijms-25-09088-g001.jpg

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