Literature DB >> 22490596

A high-fat diet reverses improvement in glucose tolerance induced by duodenal-jejunal bypass in type 2 diabetic rats.

Shao-zhuang Liu1, Dong Sun, Guang-yong Zhang, Lei Wang, Teng Liu, Yu Sun, Ming-xia Li, San-yuan Hu.   

Abstract

BACKGROUND: Bariatric surgery offers successful resolution of type 2 diabetes mellitus (T2DM). However, recurrence of T2DM has been observed in a number of patients with initial resolution after bariatric surgery. This study aimed to induce reversal of the improvement of diabetes in T2DM rats after duodenal-jejunal bypass (DJB), and identify the effects of weight changes and gut hormones that might be involved.
METHODS: DJB surgery was performed in two T2DM rat models (n=20 for each group): non-obese Goto-Kakizaki (GK) rats, and moderately-obese T2DM rats induced by a combination of a high-fat diet (HFD) and low-dose streptozotocin (HS rats). The controls were sham-operated and non-treated rats. All rats were then randomly divided into HFD- and low-fat diet (LFD)-fed groups. Glucose tolerance, insulin tolerance, glucose-stimulated insulin, glucagon-like peptide-1 (GLP-1) and peptide YY (PYY) secretion, food intake and body weight were measured and compared with controls.
RESULTS: DJB surgery resulted in a significant improvement in glucose tolerance in both GK and HS rats fed with either HFD or LFD. In contrast to LFD-fed rats, improved glucose tolerance was impaired in GK and HS rats fed with an HFD, accompanied by re-impairment of insulin tolerance and failure in enhancement of insulin secretion. There was no significant difference in food intake and body weight between DJB-operated and control rats, and between HFD- and LFD-fed rats. Glucose-stimulated GLP-1 and PYY levels were significantly increased after DJB surgery; however, they were not significantly different between HFD- and LFD-fed rats.
CONCLUSION: An HFD reverses the improvement in glucose tolerance induced by DJB surgery in T2DM rats, primarily ascribing to the re-impairment of insulin sensitivity, but does not change body weight, GLP-1 and PYY levels.

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Year:  2012        PMID: 22490596

Source DB:  PubMed          Journal:  Chin Med J (Engl)        ISSN: 0366-6999            Impact factor:   2.628


  12 in total

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3.  Effects of sleeve gastrectomy with jejuno-jejunal or jejuno-ileal loop on glycolipid metabolism in diabetic rats.

Authors:  Ming-Wei Zhong; Shao-Zhuang Liu; Guang-Yong Zhang; Xiang Zhang; San-Yuan Hu
Journal:  World J Gastroenterol       Date:  2016-08-28       Impact factor: 5.742

4.  Duodenal-Jejunal bypass improves glucose homeostasis in association with decreased proinflammatory response and activation of JNK in the liver and adipose tissue in a T2DM rat model.

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5.  Alterations in gut microbiota during remission and recurrence of diabetes after duodenal-jejunal bypass in rats.

Authors:  Ming-Wei Zhong; Shao-Zhuang Liu; Guang-Yong Zhang; Xiang Zhang; Teng Liu; San-Yuan Hu
Journal:  World J Gastroenterol       Date:  2016-08-07       Impact factor: 5.742

6.  Duodenal-jejunal bypass surgery suppresses hepatic de novo lipogenesis and alleviates liver fat accumulation in a diabetic rat model.

Authors:  Haifeng Han; Chunxiao Hu; Lei Wang; Guangyong Zhang; Shaozhuang Liu; Feng Li; Dong Sun; Sanyuan Hu
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7.  Sleeve Gastrectomy with Bypass of Proximal Small Intestine Provides Better Diabetes Control than Sleeve Gastrectomy Alone Under Postoperative High-Fat Diet.

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8.  Duodenal-jejunal bypass improves glucose metabolism and adipokine expression independently of weight loss in a diabetic rat model.

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9.  Ileal Interposition in Rats with Experimental Type 2 Like Diabetes Improves Glycemic Control Independently of Glucose Absorption.

Authors:  Christian Ferdinand Jurowich; Christoph Otto; Prashanth Reddy Rikkala; Nicole Wagner; Ivana Vrhovac; Ivan Sabolić; Christoph-Thomas Germer; Hermann Koepsell
Journal:  J Diabetes Res       Date:  2015-06-22       Impact factor: 4.011

10.  Duodenal-Jejunal Bypass Surgery Reverses Diabetic Phenotype and Reduces Obesity in db/db Mice.

Authors:  Yongjun Liang; Yueqian Wang; Zhengdong Qiao; Ting Cao; Ying Feng; Lin Zhang; Peng Zhang
Journal:  Curr Chem Genom Transl Med       Date:  2017-10-31
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