Gene · 2018
Comparative analysis on liver transcriptome profiles of different methods to establish type 2 diabetes mellitus models in Guangxi Bama mini-pig.
Сравнительное исследованиеСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Wu Yanjun, Zhang Li, Liang Jing, Jiang Qinyang, Guo Yafen, Lan Ganqiu
Аннотация
AIMS/INTRODUCTION: Streptozotocin (STZ) is a permanent diabetogenic compound and often used in animal diabetes modeling. The aim of this study is to compare the liver transcriptome of type 2 diabetes models (T2DM) in Guangxi Bama Mini-pig (GBM pig) induced by STZ or Non-STZ.
RESEARCH DESIGN AND METHODS: 22 female GBM pigs were divided into 4 groups. Ctr group (4 pigs): standard diets; DM1_HH group (10 pigs): high fat and high carbohydrate diets; DM2_HS group (4 pigs): high fat and high carbohydrate diets + STZ; DM3_SH group (4 pigs): STZ + high fat and high carbohydrate diets. Fasting blood glucose (FBG), fasting insulin (FINS), triglyceride (TG) and total cholesterol (TC) were measured monthly. Glucose disappearance rate was evaluated by intravenous glucose tolerance test (IVGTT). Three pigs liver samples as biological replicates in each group were used for transcriptome sequencing analysis.
RESULTS: All pigs injected with STZ were identified as diabetic. But only 4 of 10 pigs in DM1_HH group met the diabetes model standard. The most severe insulin resistance was observed in DM2_HS group. The FBG of DM1_HH, DM2_HS, DM3_SH and Ctr group were 7.20 ± 0.17, 14.13 ± 0.45, 7.98 ± 0.99 and 4.43 ± 0.27 mmol/L, respectively; the FINS were 53.67 ± 1.82, 33.38 ± 2.32, 49.91 ± 1.50 and 39.78 ± 1.14 mU/L, respectively. Compared with DM1_HH group, liver transcriptome showed that 7 genes were up-regulated while 10 were down-regulated in DM2_HS, 16 genes were up-regulated while 14 were down-regulated in DM3_SH. There were 4 co-expressive genes in DM2_HSvsDM1_HH and DM3_SHvsDM1_HH, including cystein rich 61 gene (CYR61), ribosomal protein L15 gene (RPL15), regulator of G protein signaling 1 gene (RGS1) and LOC102166695 gene.
CONCLUSION: STZ can rapidly induce T2DM model in GBM pig, but STZ caused abnormal expression of genes in the liver.
RESEARCH DESIGN AND METHODS: 22 female GBM pigs were divided into 4 groups. Ctr group (4 pigs): standard diets; DM1_HH group (10 pigs): high fat and high carbohydrate diets; DM2_HS group (4 pigs): high fat and high carbohydrate diets + STZ; DM3_SH group (4 pigs): STZ + high fat and high carbohydrate diets. Fasting blood glucose (FBG), fasting insulin (FINS), triglyceride (TG) and total cholesterol (TC) were measured monthly. Glucose disappearance rate was evaluated by intravenous glucose tolerance test (IVGTT). Three pigs liver samples as biological replicates in each group were used for transcriptome sequencing analysis.
RESULTS: All pigs injected with STZ were identified as diabetic. But only 4 of 10 pigs in DM1_HH group met the diabetes model standard. The most severe insulin resistance was observed in DM2_HS group. The FBG of DM1_HH, DM2_HS, DM3_SH and Ctr group were 7.20 ± 0.17, 14.13 ± 0.45, 7.98 ± 0.99 and 4.43 ± 0.27 mmol/L, respectively; the FINS were 53.67 ± 1.82, 33.38 ± 2.32, 49.91 ± 1.50 and 39.78 ± 1.14 mU/L, respectively. Compared with DM1_HH group, liver transcriptome showed that 7 genes were up-regulated while 10 were down-regulated in DM2_HS, 16 genes were up-regulated while 14 were down-regulated in DM3_SH. There were 4 co-expressive genes in DM2_HSvsDM1_HH and DM3_SHvsDM1_HH, including cystein rich 61 gene (CYR61), ribosomal protein L15 gene (RPL15), regulator of G protein signaling 1 gene (RGS1) and LOC102166695 gene.
CONCLUSION: STZ can rapidly induce T2DM model in GBM pig, but STZ caused abnormal expression of genes in the liver.