Department of Physical and Environmental Sciences, Texas A&M University, Corpus Christi, TX 78412, USA.
Department of Health Sciences, Texas A&M University, Corpus Christi, TX 78412, USA.
Int J Mol Sci. 2023 Mar 25;24(7):6211. doi: 10.3390/ijms24076211.
With healthcare costs rising, many affected by ailments are turning to alternative medicine for treatment. More people are choosing to complement their pharmacological regimen with dietary supplements from natural products. In this study, the compound composition of ( and the effects of combined preparations of and metformin on antioxidant activity in human skeletal muscle myoblasts (HSMMs) and human diabetic skeletal muscle myoblasts (DHSMMs) were investigated. Ultraperformance liquid chromatography fusion orbitrap mass spectrometry (UPLC-OT-FTMS) identified biologically active flavanols in . The main compounds identified in locally grown were quercetin, kaempferol, apigenin, epigallocatechin gallate (EGCG), and avicularin. Antioxidant results indicated that a combinatorial preparation of with metformin may modulate antioxidant responses by increasing the enzymatic activity of superoxide dismutase and increasing levels of reduced glutathione. A combination of 50 μM and 150 μg/mL of metformin and , respectively, resulted in a significant increase in reduced glutathione levels in non-diabetic and diabetic human skeletal muscle myoblasts and HOstress-induced human skeletal muscle myoblasts. Additionally, a treatment (400 µg/mL) alone significantly increased catalase (CAT) activity for non-diabetic and diabetic human skeletal muscle myoblasts and a HOstress-induced human skeletal muscle myoblast cell line, while significantly lowering malondialdehyde (MDA) levels. However, the treatment options were more effective at promoting cell viability after 24 h versus 72 h and did not promote cell viability after 72 h in HO-stress-induced HSMM cells. These treatment options show promise for treating oxidative-stress-mediated pathophysiological complications associated with type II diabetes.
随着医疗保健成本的上升,许多受疾病影响的人开始转向替代医学治疗。越来越多的人选择用天然产物的膳食补充剂来补充他们的药物治疗方案。在这项研究中,研究了 ( 和二甲双胍联合制剂对人骨骼肌成肌细胞(HSMM)和人糖尿病骨骼肌成肌细胞(DHSMM)抗氧化活性的化合物组成。超高效液相色谱融合轨道阱质谱(UPLC-OT-FTMS)鉴定了 中的生物活性黄烷醇。在当地种植的 中鉴定出的主要化合物为槲皮素、山奈酚、芹菜素、表没食子儿茶素没食子酸酯(EGCG)和圣草酚。抗氧化结果表明,与二甲双胍联合的制剂可能通过增加超氧化物歧化酶的酶活性和增加还原型谷胱甘肽水平来调节抗氧化反应。分别用 50 μM 和 150 μg/mL 的二甲双胍和 组合,可使非糖尿病和糖尿病人类骨骼肌成肌细胞以及 HO 应激诱导的人类骨骼肌成肌细胞中的还原型谷胱甘肽水平显著增加。此外,单独使用 (400 µg/mL)处理可显著增加非糖尿病和糖尿病人类骨骼肌成肌细胞以及 HO 应激诱导的人类骨骼肌成肌细胞中的过氧化氢酶(CAT)活性,同时显著降低丙二醛(MDA)水平。然而,与 72 h 相比,这些治疗方案在 24 h 时更能有效促进细胞活力,并且在 HO 应激诱导的 HSMM 细胞中 72 h 时不会促进细胞活力。这些治疗方案有望治疗与 2 型糖尿病相关的氧化应激介导的病理生理并发症。