MitoTEMPO 对链脲佐菌素诱导的实验性糖尿病模型中大鼠膈肌收缩参数的影响

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL European Journal of Therapeutics Pub Date : 2023-12-10 DOI:10.58600/eurjther1912
Ahmet Akkoca, S. Tuncer, M. Çelen, N. Dalkılıç
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摘要

目的:糖尿病(DM)不仅会引起高血糖,还会导致呼吸功能障碍等临床难题。膈肌的收缩可降低胸膜压力,从而对呼吸过程做出重要贡献。本研究探讨了与 DM 相关的活性氧(ROS)增加导致的膈肌等长收缩参数的功能损伤,以及线粒体特异性抗氧化剂 MitoTEMPO 对这些损伤的影响:将 12-14 周龄的 Wistar Albino 雄性大鼠随机分为三组:对照组(CON,n=6)、糖尿病组(DM,n=6)和糖尿病 + MitoTEMPO 组(MT,n=6)。给 DM 组和 MT 组大鼠注射单剂量 50 毫克/千克链脲佐菌素(STZ)。当MT组大鼠的血糖水平达到300 mg/dl时,给它们服用MitoTEMPO,剂量为0.7 mg/kg/天,持续28天。28 天结束时,从实验动物身上分离出的膈肌制备物进行等长收缩记录:虽然线粒体特异性抗氧化剂在降低 DM 中血糖水平的有效性在文献中存在争议,但 MT 组的结果有趣地表明,服用 MitoTEMPO 后,血糖水平在第四周结束时出现了统计学意义上的显著下降。此外,MitoTEMPO 对因 DM 而受损的膈肌收缩参数也有治疗作用:研究结果表明,MitoTEMPO 可用于 DM 患者的血糖控制,也可有效治疗 DM 引起的膈肌机械功能障碍。
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The Effect of MitoTEMPO on Rat Diaphragm Muscle Contraction Parameters in an Experimental Diabetes Model Induced with Streptozotocin
Objective: Diabetes Mellitus (DM) not only causes hyperglycemia but also leads to clinical challenges involving respiratory functional impairments. The contraction of the diaphragm reduces pleural pressure, thereby contributing significantly to the process of breathing. This study examines the functional impairments in diaphragm muscle isometric contraction parameters due to increased reactive oxygen species (ROS) associated with DM, as well as the effects of MitoTEMPO, a mitochondria-specific antioxidant, on these impairments. Methods: Wistar Albino male rats at 12-14 weeks of age were randomly divided into three groups: the control group (CON, n=6), the diabetes group (DM, n=6), and the diabetes + MitoTEMPO (MT, n=6) group. A single dose of 50 mg/kg streptozotocin (STZ) was administered to the rats in the DM and MT groups. When the rats in the MT group reached a blood glucose level of 300 mg/dl, they were administered MitoTEMPO at a dose of 0.7 mg/kg/day for 28 days. Isometric contraction recordings were obtained from diaphragm muscle preparations isolated from the experimental animals at the end of the 28-day period. Results: Although the effectiveness of mitochondria-specific antioxidants in reducing blood glucose levels in DM is debated in the literature, results for the MT group were interestingly indicative of a statistically significant decrease in blood glucose levels following MitoTEMPO administration at the end of the fourth week. Furthermore, MitoTEMPO exhibited therapeutic effects on diaphragm muscle contraction parameters impaired by DM. Conclusion: The findings suggest that in DM patients, MitoTEMPO could be utilized for blood glucose control and might also be effective in the treatment of DM-induced diaphragm muscle mechanical dysfunction.
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European Journal of Therapeutics
European Journal of Therapeutics MEDICINE, GENERAL & INTERNAL-
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