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作 者:段薇[1] 项芬芬 高英慧[1] 冯一丹[1] 张学梅[2]
机构地区:[1]大连大学附属中山医院内分泌科,116001 [2]大连大学医学院
出 处:《中国糖尿病杂志》2016年第12期1100-1104,共5页Chinese Journal of Diabetes
基 金:"十二五"国家科技支撑计划项目(2012BAK25B00)
摘 要:目的观察重组人p53腺病毒(rAd-p53)对两种T2DM模型鼠血糖的影响,探讨rAd-p53对糖代谢的影响及机制。方法制备HFD/STZ鼠,将HFD/STZ鼠和db/db鼠各随机分为阴性对照(rAd)组、阳性对照(胰岛素)组和rAd-p53给药组,每组8只。分别依次予rAd(4×10^(10)/ml)、中效胰岛素(1 U/kg)、rAd-p53(4×10^(10)/ml)。每72 h给药1次,连续给药3次,6周后检测各组FPG、腹腔糖耐量(IPGTT)和C-P水平。结果 rAd-p53改善HFD/STZ鼠的FPG、IPGTT,并增加C-P水平(P<0.05);但以同等剂量rAd-p53和胰岛素处置db/db鼠时,对其血糖和C-P改善不明显(P>0.05),使用3倍剂量胰岛素才能改善其血糖水平(P<0.05)。结论 rAd-p53可改善HFD/STZ鼠FPG、IPGTT和C-P水平,可能与其改善胰岛β细胞分泌缺陷、增加胰岛素释放有关。Objective To explore the possible mechanism of rAd-p53 involved in glucose metabolism by observing the different effects of rAd-p53 on high-fat diet (HFD) fed with low-dose streptozotocin (STZ) treated (HFD/STZ) mice (fl-cell dysfunction model) and db/db mice (genetic insulin resistance model). Methods The established HFD/STZ and db/db diabetic mice were respectively and randomly divided into three groups (n=8 each) : rAd (4x10^10/ml) treated group (negative control), intermediate- acting insulin(1 U/kg) injected group (positive control) and rAd-p53 (4x10^10/ml) treated group. After one week from the last STZ injection, intraperitoneal administration of rAd-p53 was begun once every 72 hours for three injections. 6 weeks later, fasting plasma glucose (FPG), IPGTT and C-peptide levels were detected. Results Compared with negative control group, rAd-p53 could significantly improve FPG, IPGTT and C-peptide in HFD/STZ mice(P〈0. 05). Insulin and rAd-p53 had 'no significant effect on the levels of FPG, IPGTT and C-peptide in db/db mice(P〈0.05). Only 3-fold and more insulin codld improve FPG and IPGTT in db/db mice (P〈0.05). Conclusion The rAd-p53 can improve FPG,IPGTT and C- peptide in HFD/STZ mice which may be associated with ameliorative β-cell function.
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