Wang Piao, Liu Yi, Zhang Tong, Yin Cheng, Kang Seok Yong, Kim Su Jin, Park Yong-Ki, Jung Hyo Won
Department of Herbology, College of Korean Medicine, Dongguk University, 38066 Gyeongju, Korea.
Korean Medicine R&D Center, Dongguk University, 38066 Gyeongju, Korea.
ACS Omega. 2021 Oct 11;6(41):26959-26968. doi: 10.1021/acsomega.1c03372. eCollection 2021 Oct 19.
Type 2 diabetes is the most common type of diabetes and causes a decline in muscle quality. In this study, we investigated the effects of the root extract of (MORE) on skeletal muscle damage in mice with high-fat-diet (HFD)/streptozotocin (STZ)-induced diabetes and the expression of myogenic and biogenesis regulatory proteins in C2C12 myoblast differentiation. An in vivo model comprised C57BL/6N mice fed HFD for 8 weeks, followed by a single injection of STZ at 120 mg/kg. MORE was administered at 100 and 200 mg/kg once daily (p.o.) for 4 weeks. The changes in body weight, calorie intake, and serum levels of glucose, insulin, total cholesterol (TCHO), HDL-cholesterol (HDL-C), LDL-cholesterol (LDL-C), aspartate transaminase (AST), and alanine aminotransferase (ALT) were investigated in diabetic mice. The histological changes in the gastrocnemius muscle were observed by H&E staining, and then the myofiber size was measured. The expression of the myogenic (MHC, myogenin, and MyoD) and biogenesis (PGC-1α, SIRT1, NRF1, and TFAM) regulatory proteins was examined in the muscle tissues and differentiated C2C12 myoblasts by Western blot, respectively. The administration of MORE at 200 mg/kg in mice with HFD/STZ-induced diabetes significantly reduced weight gains, calorie intake, insulin resistance, and serum levels of glucose, TCHO, LDL-C, AST, and ALT. MORE administration at 100 and 200 mg/kg significantly increased serum insulin and HDL-C levels in diabetic mice. In addition, MORE significantly increased the expression of MHC, myogenin, MyoD, PGC-1α, SIRT1, NRF1, and TFAM in muscle tissues as well as increased the myofiber size in diabetic mice. In C2C12 myoblast differentiation, MORE treatment at 0.5, 1, and 2 mg/mL significantly increased the expression of myogenic and biogenesis regulatory proteins in a dose-dependent manner. MORE improves diabetes symptoms in mice with HFD/STZ-induced diabetes by improving muscle function. This suggests that MORE could be used to prevent or treat diabetes along with muscle disorders.
2型糖尿病是最常见的糖尿病类型,会导致肌肉质量下降。在本研究中,我们研究了(MORE)根提取物对高脂饮食(HFD)/链脲佐菌素(STZ)诱导的糖尿病小鼠骨骼肌损伤以及C2C12成肌细胞分化过程中肌生成和生物合成调节蛋白表达的影响。体内模型包括给C57BL/6N小鼠喂食高脂饮食8周,然后单次注射120 mg/kg的链脲佐菌素。MORE以100和200 mg/kg的剂量每日一次(口服)给药4周。研究了糖尿病小鼠体重、卡路里摄入量以及血糖、胰岛素、总胆固醇(TCHO)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)血清水平的变化。通过苏木精-伊红染色观察腓肠肌的组织学变化,然后测量肌纤维大小。分别通过蛋白质印迹法检测肌肉组织和分化的C2C12成肌细胞中肌生成(MHC、肌细胞生成素和MyoD)和生物合成(PGC-1α、SIRT1、NRF1和TFAM)调节蛋白的表达。在HFD/STZ诱导的糖尿病小鼠中,以200 mg/kg的剂量给予MORE可显著降低体重增加、卡路里摄入量、胰岛素抵抗以及血糖、TCHO、LDL-C、AST和ALT的血清水平。在糖尿病小鼠中,以100和200 mg/kg的剂量给予MORE可显著提高血清胰岛素和HDL-C水平。此外,MORE可显著增加糖尿病小鼠肌肉组织中MHC、肌细胞生成素、MyoD、PGC-1α、SIRT1、NRF1和TFAM的表达,并增加肌纤维大小。在C2C12成肌细胞分化过程中,0.5、1和2 mg/mL的MORE处理以剂量依赖的方式显著增加了肌生成和生物合成调节蛋白的表达。MORE通过改善肌肉功能改善HFD/STZ诱导的糖尿病小鼠的糖尿病症状。这表明MORE可用于预防或治疗糖尿病以及肌肉疾病。