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在血糖正常和高血糖的小鼠中,坎格列净和达格列净对止血的性别依赖性影响。

Sex-dependent effects of canagliflozin and dapagliflozin on hemostasis in normoglycemic and hyperglycemic mice.

机构信息

Department of Biopharmacy and Radiopharmacy, Medical University of Bialystok, 15-222, Bialystok, Poland.

Department of Physical Chemistry, Medical University of Bialystok, 15-089, Bialystok, Poland.

出版信息

Sci Rep. 2023 Jan 17;13(1):932. doi: 10.1038/s41598-023-28225-8.

Abstract

Sodium-glucose cotransporter 2 inhibitors (SGLT2i) are antihyperglycemic drugs that decrease mortality from cardiovascular diseases. However, their effects on hemostasis in the cardioprotective effects have not been evaluated. Therefore, the effects of canagliflozin (CANA, 100 mg/kg, p.o.) and dapagliflozin (DAPA, 10 mg/kg, p.o.) on the parameters of hemostasis were investigated in female and male normoglycemic and streptozotocin (180 mg/kg, i.p.)-induced diabetic mice. CANA and DAPA reduced platelet activity in thrombus in male and female mice both normoglycemic and diabetic. CANA decreased thrombus formation in diabetic male mice, and platelet activation to ADP in diabetic female and male mice. Activation of fibrinolysis was observed in female mice, both normoglycemic and diabetic. DAPA reduced thrombus formation in diabetic male and female mice, and decreased platelet activation to ADP and fibrin formation in diabetic male mice. DAPA increased fibrin formation in normoglycemic female mice and activated fibrinolysis in diabetic female mice. CANA and DAPA exerted sex-specific effects, which were more pronounced in hyperglycemia. The antithrombotic effect of CANA and DAPA was more noticeable in male mice and could be due to platelet inhibition. The effect on coagulation and fibrinolysis was not clear since an increased coagulation and fibrinolysis were observed only in female mice.

摘要

钠-葡萄糖共转运蛋白 2 抑制剂(SGLT2i)是一种降血糖药物,可降低心血管疾病的死亡率。然而,它们在心脏保护作用中的止血作用尚未得到评估。因此,本研究旨在评估卡格列净(CANA,100mg/kg,po)和达格列净(DAPA,10mg/kg,po)对正常血糖和链脲佐菌素(180mg/kg,ip)诱导的糖尿病小鼠止血参数的影响。CANA 和 DAPA 降低了正常血糖和糖尿病雄性和雌性小鼠血栓中的血小板活性。CANA 降低了糖尿病雄性小鼠的血栓形成,以及糖尿病雌性和雄性小鼠中血小板对 ADP 的激活。在正常血糖和糖尿病雌性小鼠中观察到纤维蛋白溶解的激活。DAPA 降低了糖尿病雄性和雌性小鼠的血栓形成,降低了糖尿病雄性小鼠中血小板对 ADP 的激活和纤维蛋白形成。DAPA 增加了正常血糖雌性小鼠的纤维蛋白形成,并激活了糖尿病雌性小鼠的纤维蛋白溶解。CANA 和 DAPA 发挥了性别特异性作用,在高血糖时更为明显。CANA 和 DAPA 的抗血栓作用在雄性小鼠中更为明显,这可能与血小板抑制有关。由于仅在雌性小鼠中观察到凝血和纤维蛋白溶解增加,因此对凝血和纤维蛋白溶解的影响尚不清楚。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a777/9845220/b5c43839190f/41598_2023_28225_Fig1_HTML.jpg

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