PMID- 28233263 OWN - NLM STAT- MEDLINE DCOM- 20180215 LR - 20181202 IS - 1708-0428 (Electronic) IS - 0960-8923 (Linking) VI - 27 IP - 8 DP - 2017 Aug TI - Effects of Duodenal-Jejunal Exclusion and New Bilio-Pancreatic Diversion on Blood Glucose in Rats with Type 2 Diabetes Mellitus. PG - 2067-2072 LID - 10.1007/s11695-017-2599-4 [doi] AB - OBJECTIVE: The current study aimed to investigate the effects of duodenal-jejunal bypass (DJB), new bilio-pancreatic diversion (NBPD), and duodenal-jejunal exclusion (DJE) on blood glucose in rats with type 2 diabetes mellitus (T2DM). METHODS: Male Sprague Dawley rats were fed with high glucose, high fat food, and intraperitoneally injected with streptozotocin to establish a T2DM animal model. T2DM rats were randomly assigned into 4 groups: a sham group (n = 8), DJB group (n = 9), NBPD group (n = 10), and DJE group (n = 10). Body weight, 2-h postprandial glucose, oral glucose tolerance, fasting serum bile acid, 2-h postprandial serum bile acid, fasting insulin, 2-h postprandial insulin (INS), fasting glucagon-like peptide-1 (GLP-1), and 2-h postprandial GLP-1 were measured before and after surgery. RESULTS: Six weeks after surgery, the 2-h postprandial glucose in the DJB (16.1 +/- 6.7 mmol/L) and NBPD (19.5 +/- 5.7 mmol/L) groups decreased significantly compared to the sham group (25.8 +/- 4.9 mmol/L) (P < 0.05). There was no significant difference between the DJE (25.0 +/- 5.0 mmol/L) and sham groups (P > 0.05). Four weeks after surgery, fasting serum bile acid in the DJB group (60.6 +/- 11.4 mumol/L) and NBPD group (54.4 +/- 7.64 mumol/L) was significantly higher than that in the sham group (34.3 +/- 6.98 mumol/L; P < 0.05). However, fasting GLP-1, 2-h postprandial GLP-1, and insulin remained unchanged at different time points after surgery (P > 0.05). Body weight remained stable after surgery in all 4 groups (P > 0.05). CONCLUSION: NBPD plays a major role in the therapy of T2DM with DJB. NBPD may significantly increase fasting serum bile acid in T2DM rats, an action that may be one of the mechanisms underlying the therapeutic effects of DJB on T2DM. FAU - Weng, Shan Geng AU - Weng SG AD - Hepatopancreatobiliary Surgery Department, the First Affiliated Hospital of Fujian Medical University, No 20 Chazhong Road, Fuzhou City, Fujian, People's Republic of China. shangeng@sina.com. FAU - Zhang, Bin AU - Zhang B AD - Hepatopancreatobiliary Surgery Department, the First Affiliated Hospital of Fujian Medical University, No 20 Chazhong Road, Fuzhou City, Fujian, People's Republic of China. FAU - Wang, Xiaojian AU - Wang X AD - Hepatopancreatobiliary Surgery Department, the First Affiliated Hospital of Fujian Medical University, No 20 Chazhong Road, Fuzhou City, Fujian, People's Republic of China. FAU - Chen, Hao AU - Chen H AD - Hepatopancreatobiliary Surgery Department, the First Affiliated Hospital of Fujian Medical University, No 20 Chazhong Road, Fuzhou City, Fujian, People's Republic of China. LA - eng PT - Journal Article PL - United States TA - Obes Surg JT - Obesity surgery JID - 9106714 RN - 0 (Blood Glucose) RN - 0 (Insulin) RN - 5W494URQ81 (Streptozocin) RN - 89750-14-1 (Glucagon-Like Peptide 1) SB - IM MH - Animals MH - Biliopancreatic Diversion/*methods MH - Blood Glucose/*metabolism MH - Diabetes Mellitus, Experimental/metabolism/pathology/*surgery MH - Diabetes Mellitus, Type 2/metabolism/pathology/*surgery MH - Duodenum/*surgery MH - Gastric Bypass/methods MH - Glucagon-Like Peptide 1/blood MH - Glucose Tolerance Test MH - Insulin/blood MH - Insulin Resistance MH - Jejunum/*surgery MH - Male MH - Rats MH - Rats, Sprague-Dawley MH - Streptozocin OTO - NOTNLM OT - Bile acid OT - Duodenal-jejunal exclusion OT - Glucagon-like peptide-1 OT - New bilio-pancreatic diversion EDAT- 2017/02/25 06:00 MHDA- 2018/02/16 06:00 CRDT- 2017/02/25 06:00 PHST- 2017/02/25 06:00 [pubmed] PHST- 2018/02/16 06:00 [medline] PHST- 2017/02/25 06:00 [entrez] AID - 10.1007/s11695-017-2599-4 [pii] AID - 10.1007/s11695-017-2599-4 [doi] PST - ppublish SO - Obes Surg. 2017 Aug;27(8):2067-2072. doi: 10.1007/s11695-017-2599-4.