栎瘿提取物对糖尿病大鼠甲状腺和睾丸功能的影响

Salam H. Ibrahim
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引用次数: 1

摘要

据报道,糖尿病伴有甲状腺和睾丸功能障碍。本研究的目的是研究感染栎提取物对糖尿病大鼠甲状腺和睾丸功能的影响。将16只大鼠随机分为四组,分别为正常对照组、糖尿病未治疗对照组、口服500 mg/kg BW和1000 mg/kg BW的糖尿病治疗组,为期15天。评估血清血糖、促甲状腺激素(TSH)、三碘甲状腺原氨酸(T3)、甲状腺素(T4)、睾酮(T)和黄体生成素(LH)。在实验期结束时,对大鼠实施安乐死,以进行甲状腺和睾丸的组织病理学分析。此外,用免疫组织化学方法评估甲状腺转录因子-1(TTF-1)在大鼠甲状腺中的表达。糖尿病大鼠(DC)血清血糖水平的显著升高通过用QIg提取物(500mg和100mg/kg BW)处理而显著降低,几乎降至正常水平。用QIg提取物(500mg和100mg/kg体重)治疗15天后,降低的甲状腺激素T3和T4均显著恢复。而QIg提取物(500mg和100mg/kg BW)治疗的糖尿病大鼠血清睾酮浓度显著降低。糖尿病大鼠的组织病理学分析显示,甲状腺和睾丸结构发生了广泛的形态学变化,通过用QIg提取物治疗大鼠,这些结构几乎完全恢复正常。此外,结果显示TTF-1在糖尿病大鼠的甲状腺中过表达,在用QIg提取物治疗15天后,其恢复到正常表达。这些发现可能为QIg提取物作为一种有前途的治疗甲状腺和睾丸功能糖尿病并发症的药物的潜在作用提供新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Quercus infectoria Galls Extract on Thyroid Gland and Testicular Functions in Diabetic Rats
Diabetes mellitus has been reported to be accompanied by thyroid and testicular dysfunctions. The objective of this study was to investigate the effect of Quercus infectoria galls (QIg) extract on the thyroid gland and testicular functions in diabetic rats. Sixteen rats were randomly divided into four equal groups, consisting of normal control, diabetic untreated control, diabetic treated with oral administration of 500 mg/kg BW and 1000 mg/kg BW, respectively for 15 days. Serum blood glucose, thyroid stimulating hormone (TSH), triiodothyronine (T3), thyroxine (T4), testosterone (T), and luteinizing hormone (LH) were assessed. At the end of the experimental period, the rats were euthanized for histopathological analysis of thyroid gland and testis. Furthermore, immunohistochemistry was used to assess the expression of thyroid transcription factor-1 (TTF-1) in the thyroid gland of rats. The significant increase in serum blood glucose level in diabetic rats (DC) was markedly decreased by treatment with QIg extract (500 mg and 100 mg/kg BW) almost to the normal level. The reduced thyroid hormones, both the T3 and T4 were significantly recovered after 15 days of treatment with QIg extract (500 mg and 100 mg/kg BW). Whereas serum concentration of testosterone was significantly reduced in diabetic rats with QIg extract (500 mg and 100 mg/kg BW) treatment. Histopathological analysis of diabetic rats showed a wide range of morphological alterations in thyroid gland and testicular structures, which were almost completely, restored back to normal by treatment of rats with QIg extract. Furthermore, results showed overexpression of TTF-1 in the thyroid gland of diabetic rats, which was recovered back to normal expression after 15 days of treatment with QIg extract. These findings may provide new insights into the potential role of QIg extract as a promising therapeutic agent against diabetic complications in thyroid gland and testicular functions.
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