[1]李娜娜 任寿安.慢性间歇低氧对大鼠肝细胞IRS-2、FoxO1表达的影响[J].国际内分泌代谢杂志,2015,(01):1-5.[doi:10.3760/cma.j.issn.1673-4157.2015.01.001]
 Li Nana,Ren Shouan.Effects of chronic intermittent hypoxia on IRS-2 and FoxO1 expression in rat heptocytes[J].International Journal of Endocrinology and Metabolism,2015,(01):1-5.[doi:10.3760/cma.j.issn.1673-4157.2015.01.001]
点击复制

慢性间歇低氧对大鼠肝细胞IRS-2、FoxO1表达的影响()
分享到:

《国际内分泌代谢杂志》[ISSN:1673-4157/CN:12-1383/R]

卷:
期数:
2015年01
页码:
1-5
栏目:
论著
出版日期:
2015-01-20

文章信息/Info

Title:
Effects of chronic intermittent hypoxia on IRS-2 and FoxO1 expression in rat heptocytes
作者:
李娜娜 任寿安
030001太原,山西医科大学(李娜娜);030001太原,山西医科大学第一医院呼吸科(任寿安)
Author(s):
Li Nana Ren Shouan
(Shanxi Medical University, Taiyuan 030001, China)
关键词:
慢性间歇低氧IRS-2FoxO1胰岛素抵抗
Keywords:
Chronic intermittent hypoxiaIRS-2FoxO1Insulin resistance
DOI:
10.3760/cma.j.issn.1673-4157.2015.01.001
摘要:
目的 观察慢性间歇低氧条件下,大鼠肝细胞形态学变化及胰岛素受体底物-2(IRS-2)、叉头框蛋白O1(FoxO1)的蛋白表达,并探讨IRS-2、FoxO1与胰岛素抵抗的相关性。方法 取24只6周龄健康雄性Sprauge-Dawley大鼠,采用随机数字表法分为正常对照组(NC组)、慢性间歇低氧4周组(CIH4组)、慢性间歇低氧8周组(CIH8组),每组8只。CIH4组和CIH8组暴露于间歇低氧舱内:最低氧浓度6%~8%,持续时间8h/d。NC组无间歇低氧暴露正常饲养,CIH4组、CIH8组和NC组分别于第4周、第8周及第8周禁食12h后测定空腹血糖、空腹胰岛素水平,并采用稳态模型评估胰岛素抵抗指数(HOMA-IR)和胰岛素敏感性指数(ISI)评价胰岛素抵抗,对肝组织行HE染色观察形态学变化,采用免疫组织化学方法测定肝细胞IRS-2、FoxO1蛋白表达,以平均灰度值表示其蛋白表达量,二者成反比关系。结果与NC组相比,CIH4组、CIH8组空腹血糖、胰岛素、HOMA-IR升高,ISI降低,且CIH8组更为显著,差异有统计学意义(F=50.23~90.26,P均<0.05)。与NC组相比,CIH4组与CIH8组IRS-2蛋白表达降低,FoxO1蛋白表达增高且在核内重新分布,CIH8组更为显著,差异有统计学意义(F=69.46,618.94,P均<0.05)。Pearson相关分析显示:HMOA-IR与IRS-2平均灰度值呈正相关(r=0.857,P<0.05),与FoxO1平均灰度值呈负相关(r=-0.926, P<0.05),ISI与IRS-2平均灰度值呈负相关(r=-0.823,P<0.05),与FoxO1平均灰度值呈正相关(r=0.848,P<0.05)。结论慢性间歇低氧条件下,大鼠肝细胞受损并发生胰岛素抵抗,同时IRS-2和FoxO1蛋白表达异常,且随暴露时间延长肝细胞损伤程度及胰岛素抵抗程度均逐渐加重。
Abstract:
Objective To observe the histomorphologic alteration and expression of insulin receptor substrate (IRS)-2 and FoxO1 in rat heptocytes, and investigate the association of IRS-2 and FoxO1 with insulin resistance induced by chronic intermitted hypoxia. Methods Twentyfour healthy male Sprauge Dawley rats at 6 week age were divided into normal control group (NC group), chronic intermittent hypoxia for 4 weeks group (CIH4 group) and chronic intermittent hypoxia for 8 weeks group (CIH8 group) according to random number table, with 8 rats in each group. CIH4 group and CIH8 group were placed in intermittent low oxygen cabin for 8 hours per day, the minimum oxygen concentration was 6%-8%. NC group was placed in normal air cabin. Fasting blood glucose and fasting insulin level were measured on 4th week, 8th week and after an overnight fast of 12 hours on 8th week in CIH4, CIH8 and NC group, respectively. Homeostatic model assessment of insulin resistance index (HOMA-IR) and insulin sensitive index (ISI) were used to evaluate insulin resistance. HE staining was used for morphologic study of liver. IRS-2 and FoxO1 expression in heptocytes were analyzed by immunohistochemistry. Average gray value was used to represent the protein expression, and which was inversely proportional to average gray value. Results Compared with NC group, CIH4 and CIH8 group had elevated fasting blood glucose, fasting insulin, HOMA-IR, and reduced ISI, especially in CIH8 group (F=50.23-90.26, all P<0.05). Compared with NC group, the expression of IRS-2 decreased in CIH4 and CIH8 group;the expression of FoxO1 increased in CIH4 and CIH8 group with the redistribution in the nucleus, especially in CIH8 group(F=69.46,618.94, all P<0.05). Pearson correlation analysis showed that HOMA-IR was positively correlated with the average gray value of IRS-2 (r=0.857,P<0.05), but was negatively correlated with the average gray value of FoxO1 (r=-0.926,P<0.05). ISI was negatively correlated with the average gray value of IRS-2(r=-0.823, P<0.05) and was positively correlated with the average gray value of FoxO1 (r=0.848,P<0.05). Conclusions In intermittent hypoxia, the liver is damaged along with the occurrence of insulin resistance and the abnormal expression of IRS-2 and FoxO1, which are aggravated with the exposure time of hypoxia.

参考文献/References:

[1]张秀娟,李庆云,徐华俊. 睡眠呼吸暂停模式间歇低氧动物模型的建立及应用[J].中华结核和呼吸杂志, 2011,34(10):777-779.
[2]Jain SK,Kahlon G,Morehead L,et al.The effect of sleep apnea and insomnia on blood levels of leptin, insulin resistance, IP-10, and hydrogen sulfidein type 2 diabetic patients[J].Metab Syndr Relat Disord,2012,10(5):331-336.
[3]Resnick HE, Redline S, Shahar E, et al. Diabetes and sleep disturbances: findings from the Sleep Heart Health Study[J].Diabetes Care,2003,26(3): 702-709.
[4]Kim SP, Ellmerer M, Van Citters GW, et al. Primacy of hepatic insulin resistance in the development of themetabolic syndrome induced by and isocaoric moderatefat diet in the dog[J].Diabetes,2003, 52 (10): 2453-2460.
[5]Xu W,Chi L,Row BW, et al. Increased oxidative stress is associated with chronic intermittent hypoxiamediated brain conical neuronal cell apoptosis a mouse model of sleep apnea[J]. Neurescience, 2004, 126(2):313-323.
[6]Edmison J, McCullough AJ. Pathogenesis of nonalcoholicsteatohepatitis: human data[J].Clin Liver Dis,2007,2(1):75-104.
[7]Polyzos SA, Kountouras J, Zavos C. Nonalcoholic fatty liver disease: the pathogenetic roles of insulin resistance and adipocytokines[J]. Curr Mol Med, 2009, 9(3): 299-314.
[8]Orlik B, Handzlik G, Olszanecka Glinianowicz M. The role of adipokines and insulin resistance in the pathogenesis of nonalcoholic fatty liver disease[J].Postepy Hig Med Dosw (online), 2010,64:212-219.
[9]Gconzález Navarro H,Vinué A, Vila Caballer M,et al.Molecular mechanism of atherosclerosis in metabolic syndrom: role of reduced IRS2dependent signaling[J]. Arterioseler Thromb Vasc Biol, 2008, 28(12):2187-2194.
[10]Valverde AM, Burks DJ, Fabregat I, et al. Molecular mechanisms of insulin resistance in IRS-2deficient hepatocytes[J]. Diabetes,2003,52 (9):2239-2248.
[11]Escribano O, Arribas M, Valverde AM, et al. IRS-3 mediates insulin induced glucose uptake in differentiated IRS-2(-/-) brown adipocytes[J]. Mol Cell Endocrinol, 2007, 268(1-2): 1-9.
[12]Zhang W, Patil S, Chauhan B, et al. FoxO1regulates multiple metabolie pathways in the liver: effects on gluconeogenic, glyeolytie, and lipogenic gene expression[J].Biol Chem,2006, 281(15):10105-10117.
[13]Buteau J, Spatz ML, Accili D. Transcription factor FoxO1 mediates glucagon like peptide-1 effects on pancreatic beta cell mass[J].Diabetes, 2006, 55 (5): 1190-1196.
[14]邱秀英,韩继武,李姣姣.PI3K/Akt及其靶蛋白FoxO1与非酒精性脂肪性肝病[J].现代生物医学进展, 2012, 21(23):4584-4587.

备注/Memo

备注/Memo:
基金项目:山西省自然科学基金资助项目(2013011048-4)
更新日期/Last Update: 2015-03-20