Salidroside and inflammation-linked disorders: integrative insights into the pharmacological effects and mechanistic targets.

IF 5.3 2区 医学 Q2 IMMUNOLOGY
M V N L Chaitanya, Deepshikha Patle, Sachin Kumar Singh, Avijit Mazumder, Rakesh Kumar Sindhu, Kamal Dua, Navneet Khurana, Prince Arora
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引用次数: 0

Abstract

Salidroside (SAL), a phenylpropanoid glycoside found in Rhodiola rosea L. roots, is one of the plant's most essential active components. Few studies have shown that it has many health advantages, particularly because it helps combat inflammation, prevent cell death, and protect cells from harm. Research indicated that SAL may protect cardiac myocytes from oxidative stress and enhance glucose uptake in skeletal muscle cells. It also significantly enhanced mitochondrial activity and prevented cell death in pheochromocytoma cells, SH-SY5Y neuroblastoma cells, and cardiomyocytes. Besides its advantages for cellular function, SAL is recognised for its protective effects on the heart and brain. Animal studies have shown efficacy in reducing lung damage induced by LPS and sepsis resulting from caecal ligation and puncture in murine models. SAL seems to enhance insulin resistance via activating a route that links mitochondria to AMPK, PI3K, Akt, and GSK-3β. Aqueous preparations of Rhodiola rosea have shown metabolic benefits by reducing blood glucose levels in streptozotocin-treated diabetic rats, an effect that is negated upon adrenal gland removal. The extensive array of pharmacological effects underscores the considerable therapeutic potential of SAL. Despite the well-documented advantages of SAL, research gaps persist regarding optimal dose, long-term safety, and comprehensive effectiveness comparisons in clinical environments. To assist researchers and clinicians in the biomedical sector in filling in the gaps in their knowledge and gaining a comprehensive picture of SAL's therapeutic applications and mechanisms, this review compiles the numerous results on these topics. It aims to simplify complicated material and highlight areas that need more investigation by integrating our present knowledge of SALs and their sources, biosynthesis, extraction, analysis, pharmacological effects, and molecular processes.

红景天苷和炎症相关疾病:药理作用和机制靶点的综合见解。
红景天苷(Salidroside, SAL)是一种在红景天根部发现的苯丙类苷,是红景天植物最重要的活性成分之一。很少有研究表明它对健康有很多好处,特别是因为它有助于对抗炎症,防止细胞死亡,保护细胞免受伤害。研究表明,SAL可以保护心肌细胞免受氧化应激,增强骨骼肌细胞的葡萄糖摄取。它还显著增强线粒体活性,防止嗜铬细胞瘤细胞、SH-SY5Y神经母细胞瘤细胞和心肌细胞的细胞死亡。除了对细胞功能的好处,SAL还被认为对心脏和大脑有保护作用。动物实验表明,在小鼠模型中,它能有效减少LPS引起的肺损伤和盲肠结扎穿刺引起的败血症。SAL似乎通过激活连接线粒体与AMPK、PI3K、Akt和GSK-3β的途径来增强胰岛素抵抗。红景天水制剂通过降低链脲佐菌素治疗的糖尿病大鼠的血糖水平显示出代谢益处,这种效果在肾上腺去除后被否定。广泛的药理作用强调了SAL的巨大治疗潜力。尽管SAL有充分的优势,但在最佳剂量、长期安全性和临床环境中综合有效性比较方面的研究差距仍然存在。为了帮助生物医学领域的研究人员和临床医生填补他们的知识空白,并全面了解SAL的治疗应用和机制,本综述汇编了有关这些主题的大量结果。它旨在通过整合我们目前对SALs及其来源、生物合成、提取、分析、药理作用和分子过程的知识,简化复杂的材料,突出需要更多研究的领域。
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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来源期刊
Inflammopharmacology
Inflammopharmacology IMMUNOLOGYTOXICOLOGY-TOXICOLOGY
CiteScore
8.00
自引率
3.40%
发文量
200
期刊介绍: Inflammopharmacology is the official publication of the Gastrointestinal Section of the International Union of Basic and Clinical Pharmacology (IUPHAR) and the Hungarian Experimental and Clinical Pharmacology Society (HECPS). Inflammopharmacology publishes papers on all aspects of inflammation and its pharmacological control emphasizing comparisons of (a) different inflammatory states, and (b) the actions, therapeutic efficacy and safety of drugs employed in the treatment of inflammatory conditions. The comparative aspects of the types of inflammatory conditions include gastrointestinal disease (e.g. ulcerative colitis, Crohn''s disease), parasitic diseases, toxicological manifestations of the effects of drugs and environmental agents, arthritic conditions, and inflammatory effects of injury or aging on skeletal muscle. The journal has seven main interest areas: -Drug-Disease Interactions - Conditional Pharmacology - i.e. where the condition (disease or stress state) influences the therapeutic response and side (adverse) effects from anti-inflammatory drugs. Mechanisms of drug-disease and drug disease interactions and the role of different stress states -Rheumatology - particular emphasis on methods of measurement of clinical response effects of new agents, adverse effects from anti-rheumatic drugs -Gastroenterology - with particular emphasis on animal and human models, mechanisms of mucosal inflammation and ulceration and effects of novel and established anti-ulcer, anti-inflammatory agents, or antiparasitic agents -Neuro-Inflammation and Pain - model systems, pharmacology of new analgesic agents and mechanisms of neuro-inflammation and pain -Novel drugs, natural products and nutraceuticals - and their effects on inflammatory processes, especially where there are indications of novel modes action compared with conventional drugs e.g. NSAIDs -Muscle-immune interactions during inflammation [...]
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