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诱饵技术——动脉粥样硬化治疗的有前途的工具。

Decoy Technology as a Promising Therapeutic Tool for Atherosclerosis.

机构信息

Department of Medical Biotechnology and Nanotechnology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad 9177948564, Iran.

Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

出版信息

Int J Mol Sci. 2021 Apr 23;22(9):4420. doi: 10.3390/ijms22094420.

Abstract

Cardiovascular diseases (CVDs) have been classified into several types of disease, of which atherosclerosis is the most prevalent. Atherosclerosis is characterized as an inflammatory chronic disease which is caused by the formation of lesions in the arterial wall. Subsequently, lesion progression and disruption ultimately lead to heart disease and stroke. The development of atherosclerosis is the underlying cause of approximately 50% of all deaths in westernized societies. Countless studies have aimed to improve therapeutic approaches for atherosclerosis treatment; however, it remains high on the global list of challenges toward healthy and long lives. Some patients with familial hypercholesterolemia could not get intended LDL-C goals even with high doses of traditional therapies such as statins, with many of them being unable to tolerate statins because of the harsh side effects. Furthermore, even in patients achieving target LDL-C levels, the residual risk of traditional therapies is still significant thus highlighting the necessity of ongoing research for more effective therapeutic approaches with minimal side effects. Decoy-based drug candidates represent an opportunity to inhibit regulatory pathways that promote atherosclerosis. In this review, the potential roles of decoys in the treatment of atherosclerosis were described based on the in vitro and in vivo findings.

摘要

心血管疾病(CVDs)已被分类为几种疾病,其中动脉粥样硬化最为常见。动脉粥样硬化的特征是一种炎症性慢性疾病,由动脉壁病变的形成引起。随后,病变的进展和破坏最终导致心脏病和中风。动脉粥样硬化的发展是西方社会大约 50%的所有死亡的根本原因。无数的研究旨在改善动脉粥样硬化治疗的治疗方法;然而,它仍然是全球健康和长寿挑战的首要问题。一些家族性高胆固醇血症患者即使使用大剂量的传统疗法(如他汀类药物)也无法达到预期的 LDL-C 目标,其中许多人因副作用严重而无法耐受他汀类药物。此外,即使在达到 LDL-C 目标水平的患者中,传统疗法的残余风险仍然很高,因此强调了需要进行持续研究,以找到副作用最小但更有效的治疗方法。基于诱饵的药物候选物代表了抑制促进动脉粥样硬化的调节途径的机会。在这篇综述中,根据体外和体内的发现,描述了诱饵在动脉粥样硬化治疗中的潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4f8/8122884/2a451c42b1e7/ijms-22-04420-g001.jpg

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