Chlorogenic acid ameliorates muscle wasting by upregulating mRNA expressions of calcineurin and PGC-1α in diabetic rat model.

Q3 Medicine Medical Journal of Malaysia Pub Date : 2024-08-01
K Siwi, A Tejosukmono, N Anggorowati, N Arfian, J Yunus
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引用次数: 0

Abstract

Introduction: Muscle health in diabetes mellitus (DM) is often neglected, which leads to muscle wasting. Increased reactive oxygen species in DM could decrease antioxidant enzymes such as superoxide dismutase-1 (SOD-1) and -2 (SOD-2) and inhibit calcineurin (CN) and PGC-1α signalling pathways. Chlorogenic acid (CGA) is known as a potent antioxidant and activators of CN and PGC-1α. This study aimed to determine the effect of CGA on mRNA expressions of SOD-1, SOD-2, CN and PGC-1α in inhibiting the progression of DM to muscle wasting.

Materials and methods: This study was conducted at Department of Anatomy, Faculty of Medicine, Public Health, and Nursing, Universitas Gadjah Mada starting on July 20th, 2020. A total of 24 male Wistar rats were randomly divided into six groups (four rats per group), i.e., control, DM 1.5 months (DM1.5), and DM 2 months (DM2); and DM groups treated with CGA in three different doses, namely CGA1 (12.5 mg/kg BW), CGA2 (25 mg/kg BW), and CGA3 (50 mg/kg BW). Control group was only injected with normal saline, while diabetic model was induced by intraperitoneal injection of streptozotocin. Blood glucose levels were measured twice (one week after diabetic induction and before termination). The soleus muscle tissue was harvested to analyse the mRNA expressions of SOD-1, SOD- 2, CN and PGC-1α using RT-PCR. In addition, the tissue samples were stained with immunohistochemistry for CN and haematoxylin-eosin (HE) for morphologic analysis under light microscopy.

Results: The mRNA expressions of SOD-1 and SOD-2 in the CGA1 group were relatively higher compared to the DM2 groups. The mRNA expression of CN in the CGA1 group was significantly higher compared to the DM2 group (p = 0.008). The mRNA expression of PGC-1α in the CGA1 group was significantly higher compared to the DM2 group (p = 0.025). Immunohistochemical staining showed that CNimmunopositive expression in the CGA1 group was more evident compared to the other groups. Haematoxylin-eosin staining showed that muscle tissue morphology in the CGA1 group was similar to that in the control group.

Conclusion: Chlorogenic acid at a dose of 12.5 mg/kg BW shows lower blood glucose level, good skeletal muscle tissue morphology and higher mRNA expressions of SOD-1, SOD-2, CN and PGC-1α compared to the DM groups.

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绿原酸通过上调糖尿病大鼠模型中钙调素和 PGC-1α 的 mRNA 表达,改善肌肉萎缩。
导言:糖尿病(DM)患者的肌肉健康往往被忽视,从而导致肌肉萎缩。糖尿病患者体内活性氧的增加会降低超氧化物歧化酶-1(SOD-1)和-2(SOD-2)等抗氧化酶的活性,并抑制钙神经蛋白(CN)和PGC-1α信号通路。绿原酸(CGA)是一种有效的抗氧化剂,也是 CN 和 PGC-1α 的激活剂。本研究旨在确定 CGA 对 SOD-1、SOD-2、CN 和 PGC-1α mRNA 表达的影响,以抑制 DM 向肌肉萎缩的进展:本研究于 2020 年 7 月 20 日在加札马达大学医学、公共卫生和护理学院解剖学系进行。总共 24 只雄性 Wistar 大鼠被随机分为 6 组(每组 4 只),即对照组、DM 1.5 个月组(DM1.5)和 DM 2 个月组(DM2);以及使用三种不同剂量 CGA 的 DM 组,即 CGA1(12.5 毫克/千克体重)、CGA2(25 毫克/千克体重)和 CGA3(50 毫克/千克体重)。对照组只注射生理盐水,而糖尿病模型则通过腹腔注射链脲佐菌素诱导。两次测量血糖水平(糖尿病诱导后一周和终止前)。采集比目鱼肌组织,使用 RT-PCR 分析 SOD-1、SOD-2、CN 和 PGC-1α 的 mRNA 表达。此外,还对组织样本进行了免疫组化染色(CN)和血涂片(HE),以便在光学显微镜下进行形态分析:结果:与 DM2 组相比,CGA1 组 SOD-1 和 SOD-2 的 mRNA 表达量相对较高。CGA1 组 CN 的 mRNA 表达量明显高于 DM2 组(p = 0.008)。CGA1组中PGC-1α的mRNA表达量明显高于DM2组(p = 0.025)。免疫组化染色显示,CGA1 组的 CN 免疫阳性表达比其他组更明显。血栓素-伊红染色显示,CGA1 组的肌肉组织形态与对照组相似:结论:与 DM 组相比,剂量为 12.5 mg/kg BW 的绿原酸可降低血糖水平,改善骨骼肌组织形态,提高 SOD-1、SOD-2、CN 和 PGC-1α 的 mRNA 表达量。
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
Medical Journal of Malaysia
Medical Journal of Malaysia Medicine-Medicine (all)
CiteScore
1.20
自引率
0.00%
发文量
165
期刊介绍: Published since 1890 this journal originated as the Journal of the Straits Medical Association. With the formation of the Malaysian Medical Association (MMA), the Journal became the official organ, supervised by an editorial board. Some of the early Hon. Editors were Mr. H.M. McGladdery (1960 - 1964), Dr. A.A. Sandosham (1965 - 1977), Prof. Paul C.Y. Chen (1977 - 1987). It is a scientific journal, published quarterly and can be found in medical libraries in many parts of the world. The Journal also enjoys the status of being listed in the Index Medicus, the internationally accepted reference index of medical journals. The editorial columns often reflect the Association''s views and attitudes towards medical problems in the country. The MJM aims to be a peer reviewed scientific journal of the highest quality. We want to ensure that whatever data is published is true and any opinion expressed important to medical science. We believe being Malaysian is our unique niche; our priority will be for scientific knowledge about diseases found in Malaysia and for the practice of medicine in Malaysia. The MJM will archive knowledge about the changing pattern of human diseases and our endeavours to overcome them. It will also document how medicine develops as a profession in the nation. We will communicate and co-operate with other scientific journals in Malaysia. We seek articles that are of educational value to doctors. We will consider all unsolicited articles submitted to the journal and will commission distinguished Malaysians to write relevant review articles. We want to help doctors make better decisions and be good at judging the value of scientific data. We want to help doctors write better, to be articulate and precise.
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