CAJ | 학술논문

目的研究内脂素对糖尿病大鼠骨骼肌葡萄糖转运蛋白-4（ GLUT4）和磷脂酰肌醇-3-激酶（PI3K）表达的影响并探讨其机制。方法健康雄性Wistar大鼠随机分为普通饲料组（N组）、高脂饲料组（H组）、普通饲料糖尿病模型组（N＋S组）及高脂饲料糖尿病模型组（H＋S组）。糖尿病模型组大鼠腹腔注射链脲佐菌素造模。造模成功8周后，两组糖尿病大鼠再分别随机分出一组为V＋N＋S组和V＋H＋S组，腹腔注射内脂素重组蛋白。采用实时定量RT-PCR技术检测骨骼肌GLUT4 mRNA表达， Western blot 技术检测GLUT4和PI3K蛋白表达。结果 N＋S组与N组、H＋S组与H组大鼠骨骼肌GLUT4 mRNA，GLUT4和PI3K蛋白表达水平比较明显减低（ P＜0.05）。 V＋N＋S组与N＋S组、V＋H＋S组与H＋S组比较均有所升高（P＜0.05）。结论内脂素可能通过增加PI3K的蛋白表达影响GLUT4的基因表达，导致其蛋白表达增加，从而降低血糖。
목적연구내지소대당뇨병대서골격기포도당전운단백-4（ GLUT4）화린지선기순-3-격매（PI3K）표체적영향병탐토기궤제。방법건강웅성Wistar대서수궤분위보통사료조（N조）、고지사료조（H조）、보통사료당뇨병모형조（N＋S조）급고지사료당뇨병모형조（H＋S조）。당뇨병모형조대서복강주사련뇨좌균소조모。조모성공8주후，량조당뇨병대서재분별수궤분출일조위V＋N＋S조화V＋H＋S조，복강주사내지소중조단백。채용실시정량RT-PCR기술검측골격기GLUT4 mRNA표체， Western blot 기술검측GLUT4화PI3K단백표체。결과 N＋S조여N조、H＋S조여H조대서골격기GLUT4 mRNA，GLUT4화PI3K단백표체수평비교명현감저（ P＜0.05）。 V＋N＋S조여N＋S조、V＋H＋S조여H＋S조비교균유소승고（P＜0.05）。결론내지소가능통과증가PI3K적단백표체영향GLUT4적기인표체，도치기단백표체증가，종이강저혈당。
Objective To investigate the effect of visfatin on GLUT4 mRNA expression and PI3K protein expression in skeletal muscle of diabetic rats and explore its mechanism .Methods Wistar rats were randomly divided into four groups:normal diet feeding group ( N ) , high-fat diet feeding group ( H ) , normal diet feeding +streptozotocin(STZ)-induced diabetic group(N+S)and high-fat diet feeding+STZ-induced diabetic group(H+S). Diabetic rats were given intraperitoneal injection of small dose STZ to establish models of type 2 diabetes.Visfatin were intraperitoneally injected in partial rats(V+N+S,V+H+S)from group(N+S)and group(H+S)after 8 weeks of establishment of models .Western blotting were used to assess the protein expression of PI 3K and GLUT4. GLUT4 mRNA expression were measured with real time RT-PCR.Results GLUT4 mRNA levels,GLUT4 and PI3K protein expression were decreased(P<0.05)in the Group(N+S)compared with group N,and in the Group(H+S) compared with group H,and increased(P<0.05)in the Group(V+N+S)compared with group(N+S),and in the Group(V+H+S)compared with group(H+S)respectively.Conclusion Our data show that visfatin may increase GLUT4 mRNA levels and protein expression and lower plasma glucose levels by increase PI 3K protein expression in skeletal muscle of diabetic rats .