Duodenal-Jejunal Exclusion Surgery Improves Type 2 Diabetes in a Rat Model Through Regulation of Early Glucose Metabolism

Can J Diabetes. 2020 Jul;44(5):401-406.e1. doi: 10.1016/j.jcjd.2020.02.002. Epub 2020 Apr 9.

Abstract

Objectives: Metabolic surgery has been proven to be widely effective for the control of glucose and weight in patients with type 2 diabetes and obesity. However, the effects of bariatric surgery on nonobesity type 2 diabetes and its metabolism are still unclear. This study aimed to measure the effects of duodenal-jejunal exclusion on glycometabolism in nonobese rats with type 2 diabetes and to investigate its mechanisms.

Methods: Goto-Kakizaki rats and Sprague-Dawley rats were divided into duodenal-jejunal exclusion operation groups and sham operation groups, respectively. The glucose-relative parameters were measured before and after operation. Eight weeks postoperation, the levels of the key regulators of intestinal gluconeogenesis and the crucial proteins of hepatic insulin signalling were evaluated.

Results: Postoperatively, the concentrations of blood glucose declined, and the insulin sensitivity increased significantly in rats with diabetes. However, there was no obvious reduction in weight. Eight weeks postoperatively, the mRNA levels of glucose-6-phosphatase and phosphoenolpyruvate pyruvate kinase in the jejunum and the levels of insulin receptor substrate-2 and glucose transporter-2 in the liver were significantly increased compared with the rats that had undergone the sham operation.

Conclusions: Duodenal-jejunal exclusion surgery is an effective procedure for improving glucose metabolism independent of weight loss in nonobese rats with diabetes. The molecular mechanisms might be associated with a series of processes, including intestinal gluconeogenesis and the hepatic insulin signaling pathway.

Keywords: diabète de type 2; duodenal-jejunal exclusion surgery; exclusion duodéno-jéjunale; insulin sensitivity; intestinal gluconeogenesis; néoglucogenèse intestinale; sensibilité à l'insuline; type 2 diabetes.

MeSH terms

  • Anastomosis, Surgical
  • Animals
  • Bariatric Surgery*
  • Blood Glucose / metabolism*
  • Body Weight
  • Diabetes Mellitus, Type 2 / metabolism
  • Diabetes Mellitus, Type 2 / surgery*
  • Duodenum / surgery*
  • Gluconeogenesis / genetics*
  • Glucose Tolerance Test
  • Glucose Transporter Type 2 / genetics
  • Glucose Transporter Type 2 / metabolism
  • Glucose-6-Phosphatase / genetics
  • Glucose-6-Phosphatase / metabolism
  • Insulin / metabolism
  • Insulin Receptor Substrate Proteins / genetics
  • Insulin Receptor Substrate Proteins / metabolism
  • Insulin Resistance
  • Intracellular Signaling Peptides and Proteins / genetics
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Jejunum / metabolism
  • Jejunum / surgery*
  • Liver / metabolism*
  • Phosphoenolpyruvate Carboxykinase (GTP) / genetics
  • Phosphoenolpyruvate Carboxykinase (GTP) / metabolism
  • RNA, Messenger / metabolism
  • Rats
  • Stomach / surgery*

Substances

  • Blood Glucose
  • Glucose Transporter Type 2
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Intracellular Signaling Peptides and Proteins
  • Irs2 protein, rat
  • RNA, Messenger
  • Slc2a2 protein, rat
  • Glucose-6-Phosphatase
  • Pck1 protein, rat
  • Phosphoenolpyruvate Carboxykinase (GTP)