Department of Pharmacology and Toxicology, Zydus Research Center, Sarkhej-Bavla N.H. No. 8A, Moraiya, Ahmedabad 382213, India.
Int J Endocrinol. 2011;2011:908367. doi: 10.1155/2011/908367. Epub 2011 Nov 24.
T(3) (3,5,3'-triiodothyronine) has drawn relatively little attention in relation to cardiovascular (CVS) diseases. The present study was designed to evaluate the cardioprotective action of T(3) in isoproterenol-(ISO-) induced cardiac toxicity. Female Wistar rats were exposed with ISO (100 mg/kg, body weight, subcutaneously) for 2 days at the interval of 24 h followed by T(3) (3 μg/kg, body weight, orally) treatment for 3 days. Positive control rats received only ISO (100 mg/kg, body weight, subcutaneously) for 2 days at the interval of 24 hrs. Control group animals received normal saline as a vehicle. As expected, ISO-induced significant changes were observed in low-density lipoprotein, total cholesterol, ALT, CK-MB to TCK ratio, and prolongation of QT interval in electrocardiogram, which is toward normalization after T(3) treatment. Lower heart weight, upregulation of cardiac myosin heavy chain alpha (MHC-α), and reduced inflammatory cell infiltration, myonecrosis, vacuolar changes, and a trend toward normal cardiac muscle fiber architecture in microscopic examination of cardiac tissue further support the cardioprotective effect of T(3).
T(3)(三碘甲状腺原氨酸)在心血管(CVS)疾病方面的研究相对较少。本研究旨在评估 T(3) 在异丙肾上腺素(ISO)诱导的心脏毒性中的心脏保护作用。雌性 Wistar 大鼠皮下注射 ISO(100mg/kg,体重),间隔 24 小时,连续 2 天,随后口服 T(3)(3μg/kg,体重)连续 3 天。阳性对照组大鼠仅在 24 小时间隔内皮下注射 ISO(100mg/kg,体重)。对照组动物给予生理盐水作为载体。正如预期的那样,ISO 诱导的低密度脂蛋白、总胆固醇、ALT、CK-MB 与 TCK 比值以及心电图 QT 间期延长等变化在 T(3)治疗后趋于正常。心脏重量降低,心肌肌球蛋白重链 alpha(MHC-α)上调,炎症细胞浸润、肌坏死、空泡变化减少,以及心肌组织显微镜检查中心肌纤维结构趋于正常,进一步支持 T(3)的心脏保护作用。