GLUT4, glucose transporter type 4

  • 文章类型: Journal Article
    本研究旨在探讨不同分子量铁皮石斛叶多糖缓解糖脂代谢异常的可能机制,T2D小鼠的器官功能障碍和肠道菌群失调。用超滤膜从铁皮石斛叶多糖LDOP-A和LDOP-B中分离出两个部分。这里,我们提供的数据支持口服LDOP-A和LDOP-B改善高血糖症,抑制胰岛素抵抗,降低脂质浓度,改善β细胞功能。较低分子量的LDOP-A对糖尿病的疗效优于LDOP-B,同时结肠短链脂肪酸(SCFA)水平增加,即丁酸盐,Firmicutes与拟杆菌门的比例降低,增加了肠道有益细菌的丰度,乳酸菌,双歧杆菌和Akkermansia。这些结果表明,LDOP-A比LDOP-B在改善T2D方面具有更强的作用,这可能与肠道菌群微观结构变化产生的SCFA水平明显改善有关。
    The present study aimed to explore the possible mechanisms underlying Dendrobium officinale leaf polysaccharides of different molecular weight to alleviate glycolipid metabolic abnormalities, organ dysfunction and gut microbiota dysbiosis of T2D mice. An ultrafiltration membrane was employed to separate two fractions from Dendrobium officinale leaf polysaccharide named LDOP-A and LDOP-B. Here, we present data supporting that oral administration of LDOP-A and LDOP-B ameliorated hyperglycemia, inhibited insulin resistance, reduced lipid concentration, improved β-cell function. LDOP-A with lower molecular weight exhibited improved effect on diabetes than LDOP-B, concurrent with increased levels of colonic short-chain fatty acids (SCFAs) i.e., butyrate, decreased ratio of Firmicutes to Bacteroidetes phyla, and increased abundance of the gut beneficial bacteria i.e., Lactobacillus, Bifidobacterium and Akkermansia. These results suggest that LDOP-A possesses a stronger effect in ameliorating T2D than LDOP-B which may be related to the distinct improved SCFAs levels produced by the change of intestinal flora microstructure.
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  • 文章类型: Journal Article
    糖尿病肾病(DN)是糖尿病的严重并发症,是终末期肾病的主要病因,这给全世界的人类社会造成了严重的健康问题和巨大的经济负担。常规战略,如肾素-血管紧张素-醛固酮系统阻断,血糖水平控制,和减轻体重,在许多DN管理的临床实践中,可能无法获得令人满意的结果。值得注意的是,由于多目标函数,中药作为DN治疗的主要或替代疗法具有很好的临床益处。越来越多的研究强调确定中药的生物活性化合物和肾脏保护作用的分子机制。参与糖/脂代谢调节的信号通路,抗氧化,抗炎,抗纤维化,足细胞保护已被确定为重要的作用机制。在这里,在回顾临床试验结果后,我们总结了中药及其生物活性成分在治疗和管理DN中的临床疗效,系统评价,和荟萃分析,对动物和细胞实验中报道的相关潜在机制和分子靶标进行了彻底讨论。我们旨在全面了解中药对DN的保护作用。
    Diabetic nephropathy (DN) has been recognized as a severe complication of diabetes mellitus and a dominant pathogeny of end-stage kidney disease, which causes serious health problems and great financial burden to human society worldwide. Conventional strategies, such as renin-angiotensin-aldosterone system blockade, blood glucose level control, and bodyweight reduction, may not achieve satisfactory outcomes in many clinical practices for DN management. Notably, due to the multi-target function, Chinese medicine possesses promising clinical benefits as primary or alternative therapies for DN treatment. Increasing studies have emphasized identifying bioactive compounds and molecular mechanisms of reno-protective effects of Chinese medicines. Signaling pathways involved in glucose/lipid metabolism regulation, antioxidation, anti-inflammation, anti-fibrosis, and podocyte protection have been identified as crucial mechanisms of action. Herein, we summarize the clinical efficacies of Chinese medicines and their bioactive components in treating and managing DN after reviewing the results demonstrated in clinical trials, systematic reviews, and meta-analyses, with a thorough discussion on the relative underlying mechanisms and molecular targets reported in animal and cellular experiments. We aim to provide comprehensive insights into the protective effects of Chinese medicines against DN.
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  • 文章类型: Journal Article
    糖尿病或糖尿病是一种复杂或多基因的疾病,其特征在于肝脏和外周组织中的葡萄糖水平升高(高血糖症)和胰岛素分泌不足或胰岛素抵抗。噻唑烷-2,4-二酮(TZD)是一种特殊的支架和在药物发现领域的杰出杂环部分,这为探索该部分作为抗糖尿病药物提供了各种机会。在过去的几年里,已经采取了各种新颖的合成方法来合成不同的衍生物,以探索它们作为没有副作用的更有效的抗糖尿病药(即,水肿,体重增加,和膀胱癌)临床使用的TZD(吡格列酮和罗格列酮)。在这次审查中,已经努力总结TZD衍生物的各种合成策略的最新研究工作以及TZD与其他类别的抗糖尿病药物组合的生物学意义和临床研究。这篇综述还强调了结构-活性关系和分子对接研究,以传达各种合成的新型衍生物与其受体位点的相互作用。
    Diabetes or diabetes mellitus is a complex or polygenic disorder, which is characterized by increased levels of glucose (hyperglycemia) and deficiency in insulin secretion or resistance to insulin over an elongated period in the liver and peripheral tissues. Thiazolidine-2,4-dione (TZD) is a privileged scaffold and an outstanding heterocyclic moiety in the field of drug discovery, which provides various opportunities in exploring this moiety as an antidiabetic agent. In the past few years, various novel synthetic approaches had been undertaken to synthesize different derivatives to explore them as more potent antidiabetic agents with devoid of side effects (i.e., edema, weight gain, and bladder cancer) of clinically used TZD (pioglitazone and rosiglitazone). In this review, an effort has been made to summarize the up to date research work of various synthetic strategies for TZD derivatives as well as their biological significance and clinical studies of TZDs in combination with other category as antidiabetic agents. This review also highlights the structure-activity relationships and the molecular docking studies to convey the interaction of various synthesized novel derivatives with its receptor site.
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