亲水性他汀类药物对链脲霉素诱导的糖尿病大鼠体内脂肪连素、瘦素、粘蛋白和血管紧张素水平的影响

IF 3.1 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Hacer Kayhan Kaya, Berjan Demirtas
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引用次数: 0

摘要

他汀类药物可能会通过脂肪因子影响葡萄糖代谢。本研究旨在测定亲水性他汀类药物对糖尿病大鼠体内几种脂肪因子水平的影响。Wistar 白化大鼠分为四组:健康对照组、未治疗糖尿病组、普伐他汀治疗糖尿病组和罗伐他汀治疗糖尿病组。腹腔注射 STZ 诱导糖尿病。之后,给糖尿病大鼠服用普伐他汀或罗苏伐他汀,剂量为 20 毫克/千克/天,持续 8 周。实验结束时,测量了大鼠的体重、空腹血糖水平、血清胰岛素水平、胰岛素抵抗以及血清脂肪连素、瘦素、粘蛋白和血管紧张素水平。未经治疗的糖尿病组空腹血糖和胰岛素抵抗水平明显高于对照组,而胰岛素水平和体重则明显低于对照组。糖尿病导致脂肪连素、瘦素和血管紧张素水平明显下降,但粘脂水平明显上升。普伐他汀治疗可明显增加体重,降低空腹血糖水平,而罗伐他汀可降低体重,但不影响空腹血糖水平。普伐他汀可使脂肪连接蛋白和维aspin水平明显增加。然而,罗伐他汀并不影响脂肪生成素的水平,但会导致血管紧张素水平显著下降。普伐他汀和洛伐他汀都能降低瘦素和粘脂水平。总之,普伐他汀能更有效地改善糖尿病大鼠的空腹血糖水平和体重,这可能是通过增加脂肪连接蛋白和vaspin水平实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of hydrophilic statins on adiponectin, leptin, visfatin, and vaspin levels in streptozocin-induced diabetic rats.

Statins may affect glucose metabolism through adipokines. The aim of this study was to measure the effects of hydrophilic statins on the levels of several adipokines in diabetic rats. Wistar albino rats were divided into four groups: healthy control, untreated diabetic, diabetic treated with pravastatin, and diabetic treated with rosuvastatin. Diabetes was induced by intraperitoneal injection of STZ. Thereafter, 20 mg/kg/day doses of either pravastatin or rosuvastatin were administered to the treated diabetic rats for 8 weeks. At the end of the experiment, the body weights, fasting blood glucose levels, serum insulin levels, and insulin resistance, as well as the serum adiponectin, leptin, visfatin, and vaspin levels, were measured. Fasting blood glucose and insulin resistance levels were significantly higher, whereas insulin levels and body weight were significantly lower in the untreated diabetic group than in the control group. Diabetes caused significant decreases in adiponectin, leptin, and vaspin levels but a significant increase in visfatin levels. Pravastatin treatment significantly increased body weight and decreased fasting blood glucose levels, whereas rosuvastatin decreased body weight but did not affect fasting blood glucose levels. Pravastatin caused significant increases in both adiponectin and vaspin levels. However, rosuvastatin did not affect the adiponectin level but caused a significant decrease in the vaspin levels. Both pravastatin and rosuvastatin treatments decreased the leptin and visfatin levels. In conclusion, pravastatin is more effective at improving fasting blood glucose levels and body weight in diabetic rats, probably by increasing adiponectin and vaspin levels.

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来源期刊
CiteScore
6.20
自引率
5.60%
发文量
142
审稿时长
4-8 weeks
期刊介绍: Naunyn-Schmiedeberg''s Archives of Pharmacology was founded in 1873 by B. Naunyn, O. Schmiedeberg and E. Klebs as Archiv für experimentelle Pathologie und Pharmakologie, is the offical journal of the German Society of Experimental and Clinical Pharmacology and Toxicology (Deutsche Gesellschaft für experimentelle und klinische Pharmakologie und Toxikologie, DGPT) and the Sphingolipid Club. The journal publishes invited reviews, original articles, short communications and meeting reports and appears monthly. Naunyn-Schmiedeberg''s Archives of Pharmacology welcomes manuscripts for consideration of publication that report new and significant information on drug action and toxicity of chemical compounds. Thus, its scope covers all fields of experimental and clinical pharmacology as well as toxicology and includes studies in the fields of neuropharmacology and cardiovascular pharmacology as well as those describing drug actions at the cellular, biochemical and molecular levels. Moreover, submission of clinical trials with healthy volunteers or patients is encouraged. Short communications provide a means for rapid publication of significant findings of current interest that represent a conceptual advance in the field.
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