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Liraglutide,GLP-1受體激動劑

2022-09-27 11:11 作者:BIOFOUNT范德生物  | 我要投稿

Liraglutide(204656-20-2)是人胰高血糖素樣肽 (GLP-1) 的長效類似物。它作為GLP-1受體激動劑。利拉魯肽在體外減弱人血管內(nèi)皮細胞中纖溶酶原激活物抑制劑1型和血管粘附分子表達的誘導,并可能防止內(nèi)皮細胞功能障礙。Liraglutide通過血管內(nèi)皮細胞系抑制 TNFα 誘導的 ICAM-1 和 VCAM-1 mRNA 和蛋白質表達。

溶解度:生物體外In Vitro:H2O5 mg/mL(1.33 mM;ultrasonic and adjust pH to 8 with NaOH)

性狀:Solid power

儲藏條件:Storage conditionsprotect from light避光 粉末Powder: -80°C 2years年 -20°C 1 year / In solvent溶液中: -80°C 6 months月 -20°C 1 month月

案例:

Figure 1?Effects of liraglutide and telmisartan on body weight, blood sugar, MDA, SOD, NT-pro-BNP, and cardiac hypertrophy after abdominal aortic constriction (AAC). (A) body weight and blood glucose were measured among different groups. (B?and?C) Levels of MDA, SOD, and NT-pro-BNP activity in myocardial tissue were determined using Elisa kits. (D) MSA in series was measured morphometrically at a HPF (original magnification: 200; scale bars: 100 μm). (E) Heart/body weight ratio (HW/BW, mg/g) was calculated by weight. Values are mean±SEM (n=6/group). *p<0.05 AAC vs Sham;?#p<0.05 liraglutide (Lira) or telmisartan (Telmi) vs AAC.?Abbreviations:?MDA, malonaldehyde; SOD, superoxide dismutase; NT-pro-BNP, N-terminal pro-B-type natriuretic peptide; MSA, myocyte sectional area.


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