The Effects of Sleeve Gastrectomy on Glucose Metabolism and Glucagon-Like Peptide 1 in Goto-Kakizaki Rats

Li, Laiyuan; Wang, Xiaolin; Bai, Liangliang; Yu, Huichuan; Huang, Zenghong; Huang, Anpei; Luo, Yanxin; Wang, Jianping

doi:https://doi.org/10.1155/2018/1082561

Journal of Diabetes Research

On this page

Abstract Introduction Methods Results Discussion Additional Points Conflicts of Interest Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2018 | Article ID 1082561 | https://doi.org/10.1155/2018/1082561

The Effects of Sleeve Gastrectomy on Glucose Metabolism and Glucagon-Like Peptide 1 in Goto-Kakizaki Rats

Laiyuan Li,^1,2Xiaolin Wang,²Liangliang Bai,²Huichuan Yu,^1,2Zenghong Huang,^1,3Anpei Huang,⁴Yanxin Luo,^1,2and Jianping Wang^1,2

Academic Editor: Eusebio Chiefari

Received27 Aug 2017

Revised13 Oct 2017

Accepted25 Oct 2017

Published18 Feb 2018

Abstract

Purpose. To investigate the effects of sleeve gastrectomy (SG) on glucose metabolism and changes in glucagon-like peptide 1 (GLP-1) in Goto-Kakizaki (GK) rats. Methods. GK rats were randomly assigned to one of three groups: SG, SG pair-fed plus sham surgery (PF-sham), and ad libitum-fed no surgery (control). Food intake, body weight, blood glucose, GLP-1 and insulin levels, and GLP-1 expression in the jejunum and ileum were compared. Results. The SG rats exhibited lower postoperative food intake, body weight, and fasting glucose than did the control rats (). SG significantly improved glucose and insulin tolerance (). Plasma GLP-1 levels were higher in SG rats than in control or PF-sham rats in the oral glucose tolerance test (OGTT) (). Blood glucose levels expressed as a percentage of baseline were higher in SG rats than in control rats after exendin (9-39) administration (). The levels of GLP-1 expression in the jejunum and ileum were higher in SG rats than in PF-sham and control rats (). Conclusions. Improvement of glucose metabolism by SG was associated with increased GLP-1 secretion. SG contributes to an increase in plasma GLP-1 levels via increased GLP-1 expression in the mucosa of the jejunum and/or ileum.

1. Introduction

There were 422 million diabetic patients in 2014, and 60% of these patients were obese [1, 2]. Bariatric surgery provides sustained weight loss and glycemic control in obese patients with type 2 diabetes (T2DM), and these effects have been found to be superior to those of conventional therapy in randomized controlled trials [2, 3]. Sleeve gastrectomy (SG) has received increasing attention because of the relatively low rate of complications and the degrees of weight loss and glucose reduction, which are similar to those associated with the common Roux-en-Y gastric bypass (RYGB) [4–6]. SG involves the removal of the greater curvature of the stomach from the angle of His to the distal antrum [7]. Some of the beneficial effects of SG on glycemic homeostasis are secondary to weight loss, but the improvement in glucose control often occurs before substantial weight loss [8, 9]. Furthermore, these changes are not observed after an equivalent amount of diet-induced weight loss [10]. The hindgut hypothesis proposes that the stimulation of the distal ileum with the early arrival of partially digested nutrients is responsible for the improved glucose tolerance after bariatric surgery [11]. The remarkable changes in intestinal hormones, such as glucagon-like peptide 1 (GLP-1), are the basis of this hypothesis [12]. GLP-1 is a 30-amino acid product of the preproglucagon gene, and GLP-1 is converted by proprotein convertase 1 (PC1/3), which is encoded by the proprotein convertase subtilisin/kexin type 1 (PCSK1) gene [13–15]. GLP-1 reduces glucose excursion by inhibiting β-cell apoptosis and promoting the proliferation and stimulation of β-cell insulin secretion [16, 17]. SG produces a significantly higher resolution rate of T2DM with obesity [18]. Whether the beneficial effect of SG on glucose homeostasis is triggered by undigested nutrients in the ileum or the jejunum remains to be elucidated. This study used nonobese diabetic Goto-Kakizaki (GK) rats to investigate the effects of SG on glucose metabolism and GLP-1 levels in these GK rats.

2. Methods

2.1. Experimental Animals

Thirty nonobese, diabetic male GK rats (Chang Zhou Cavens Laboratory Animal Ltd., Changzhou, China), 12 weeks old, were individually housed and maintained with a 12 h light/dark cycle (lights off at 20:00 h) at 22–26°C and 40–60% humidity. The rats were acclimatized for two weeks and randomized to the SG, SG pair-fed plus sham surgery (PF-sham), or ad libitum-fed no surgery (control) groups. All applicable institutional and/or national guidelines for the care and use of animals were followed. The Sun Yat-sen University Animal Care and Research Committee approved all the experimental procedures.

2.2. Surgical Procedures

Anesthesia was standard among all rats that had either an SG or sham operation. SG was performed as previously described [19]. Briefly, gastric connections to the spleen and liver were released, and vascular clamps were placed along the greater curvature from the antrum to the fundus. With the use of a scalpel, approximately 80% of the total stomach was removed along the vascular clamps. The remnant stomach was sterilized with iodine, and the incision was closed with interrupted Prolene 6-0 sutures (Ningbo Medical Needle Co., Ltd., Ningbo, China). The sham surgery technique (PF-sham rats) involved the same procedure described above, except for the stomach resection. The operative time for the PF-sham rats was prolonged to ensure a degree of anesthesia-related stress equivalent to that in the rats undergoing SG.

2.3. Postoperative Care

After surgery, the GK rats were placed on a heated mat until they had fully recovered from anesthesia. All the rats received subcutaneous injections of ceftriaxone (5 mg/100 g, once daily for 3 days) and warm saline (20 ml per day for 3 days) postoperatively. The rats were provided free access to water after 24 h after surgery. Regular chow was resumed three days or even later after surgery. All the PF-sham rats were pair-fed according to the average daily food intake of the SG rats from the previous experiment. The control group rats received food ad libitum.

2.4. Body Weight and Food Intake

Body weight and food intake were measured prior to surgery and afterward for five consecutive days and then weekly between 09:00 and 11:00 h during the study period.

2.5. Glucose Tolerance Tests

The oral glucose tolerance test (OGTT) and IP injection glucose tolerance test (IPIGTT) were performed at two and seven weeks after surgery, respectively. The rats were fasted for 6 h (from 08:00 to 14:00 h) and then given an oral gavage of 25% glucose (2 g/kg) or an IP injection of 25% glucose (1.5 g/kg). Blood glucose, insulin, and GLP-1 were measured. The area under the curve (AUC) for OGTT (AUC_OGTT) was calculated starting at 0 min and ending at 120 min for each group.

2.6. Insulin Tolerance Tests

Insulin tolerance tests (ITTs) were performed at 3 and 12 weeks after surgery. The rats were fasted for 6 h and were given an IP injection of insulin (0.6 IU/kg). Glucose levels were measured at 0, 30, 60, 90, and 120 min. The ITT result was calculated as the AUC_ITT.

2.7. Intraperitoneal Injection of Exendin (9-39)

The GLP-1 receptor antagonist exendin (9-39) (American Peptide Company, CA; 50 μg/kg) was injected intraperitoneally to evaluate the effect of GLP-1 on glucose and insulin metabolism in the GK rats at six weeks postoperatively. Blood glucose and insulin concentrations were also expressed as a percentage of the baseline glucose values. Nine weeks later, an OGTT was performed after an IP injection of exendin (9-39).

2.8. GLP-1 and Insulin Measurements

Blood was collected in tubes containing an antiproteolytic cocktail every 15 min for 1 h. The plasma was separated and stored at −80°C until assayed. The plasma insulin and GLP-1 levels were measured using commercial enzyme-linked immunosorbent assay kits (Millipore, St. Charles, MO) according to the manufacturer’s instructions.

2.9. Tissue Harvesting

The beginning of the jejunum and the terminal ileum (3 cm) were removed and fully washed with sterile saline solution at 18 weeks postsurgery. Half of the tissue samples of the jejunum and ileum of each rat were fixed in 4% formalin and embedded in paraffin for immunohistochemical processing. The other half of the tissue samples was harvested and immediately frozen in liquid nitrogen and stored at −80°C for RNA extraction.

2.10. Histomorphometry and Immunohistochemistry

Tissue sections were stained with hematoxylin and eosin using standard procedures and examined by light microscopy. The villus height and width were recorded from 30 well-oriented villi on each sample slide. Formalin-fixed, paraffin-embedded sections of jejunal and ileal tissues were immunostained using an anti-GLP-1 antibody. Samples with brown-yellow granules under a light microscope were considered positive for GLP-1 expression.

2.11. RNA Isolation and Quantitative Real-Time PCR (qRT-PCR)

qRT-PCR was used to examine the relative mRNA levels of preproglucagon and PCSK1 in the jejunal and ileal segments. Total RNA was isolated from the intestinal mucosa using TRIzol (Ambion, Thermo Fisher) and purified with an RNeasy Mini kit (Qiagen, Suzhou Industrial Park, China) according to the manufacturers’ protocols. Each RNA sample was converted into cDNA using the ReverTra Ace® qPCR RT Master Mix with gDNA Remover (Toyobo, Osaka, Japan). The quantification of cDNA was performed via qRT-PCR in a LightCycler® 96 System (Roche Applied Science, Indianapolis, IN, USA) with a FastStart Essential DNA Green Master kit (Roche) under the following conditions: 20 μl per reaction, 95°C for 600 s, 45 cycles of 95°C for 10 s, 60°C for 10 s, and 72°C for 10 s.

2.12. Statistical Analyses

The results were expressed as the means ± standard deviation (SD). The AUCs for the OGTT and ITTs were calculated through trapezoidal integration. Differences between the groups were analyzed using Student’s t-test or a one-way analysis of variance (ANOVA) with the Bonferroni post hoc test, when appropriate. All statistical analyses were performed using SPSS version 21.0, and differences with were considered statistically significant.

3. Results

3.1. SG Reduces Food Intake, Body Weight, and Fasting Glucose Levels

The mean preoperative food intake, body weight, and fasting glucose level did not differ among the three groups () (Figure 1). The body weights of the SG rats after surgery were lower than those of the control rats () (Figures 1(a) and 1(b)). A significant decrease in food intake was observed in the SG rats compared with the control rats in the first week after surgery. This decrease began to reverse during the second week, but the food intake level of the SG rats was lower than that of the control rats () (Figure 1(c)). Fasting blood glucose was reduced in the SG rats after surgery compared with that in the PF-sham and control rats () (Figure 1(d)). These data suggest that SG reduced food intake, body weight, and fasting glucose levels.

(a)

(b)

(c)

(d)

3.2. SG Improves Glucose Homeostasis

Blood glucose was lower in the SG rats than in the control rats in the OGTT at 0, 15, 30, 45, 60, 90, and 120 min () (Figure 2(a)). The AUC_OGTT of the SG rats was smaller than that of the PF-sham and control rats () (Figure 2(b)). Insulin levels peaked at 15 min in all the groups, but the insulin levels were significantly lower in the SG rats than in the control rats during the OGTT at 0, 45, and 60 min () (Figure 2(c)). GLP-1 levels peaked at 15 min in all the groups, but the peak was not obvious in the PF-sham and control rats. The GLP-1 level in the SG rats was higher than that in the PF-sham or control rats at 15, 30, and 60 min () (Figure 2(d)). In the IPIGTT, the blood glucose levels increased in the three groups, but GLP-1 levels did not increase significantly, and the blood glucose and GLP-1 levels were not different among the three groups at 30, 45, and 60 min () (Figures 2(e) and 2(f)). Together, these data suggest that SG profoundly improved postprandial glucose metabolism in the GK rats, and higher insulin release was observed following increased GLP-1 after the OGTT, but not the IPIGTT, in the GK rats.

(a)

(b)

(c)

(d)

(e)

(f)

3.3. SG Improves Insulin Tolerance

An ITT analysis was performed three weeks after surgery. The blood glucose level was reduced in the SG group compared with the control and/or PF-sham groups at baseline (0) and at 30, 60, 90, and 120 min (Figure 3(a)), and the AUC_ITT of the SG rats was smaller than that of the PF-sham and control rats () (Figure 3(b)). An ITT was also performed at 12 weeks. Blood glucose in response to insulin fell to significantly lower levels in the SG rats than in the PF-sham and control rats at 0, 30, 60, 90, and 120 min () (Figure 3(c)). The blood glucose AUC_ITT was significantly lower in SG rats compared with PF-sham and control rats () (Figure 3(d)). Together, these data suggest that SG can improve insulin resistance in GK rats.

(a)

(b)

(c)

(d)

3.4. GLP-1 Stimulates Insulin Secretion

Glucose levels increased from 0 to 60 min in all groups after an IP injection of the GLP-1 (7-36) receptor antagonist exendin (9-39). However, the blood glucose level was lower in the SG group than in the control and/or PF-sham groups when expressed as an absolute value (Figure 4(a)) and as a percentage of the baseline values at 30, 45, and 60 min () (Figure 4(b)). A decrease in insulin levels was observed 15 min after exendin (9-39) administration in all the groups. The plasma insulin levels were significantly lower at baseline in the SG rats than in the control rats () (Figure 4(c)), but these levels were not significantly different from those observed in the PF-sham or control rats when expressed as a percentage of baseline at any point () (Figure 4(d)). Blood glucose levels were not significantly different between the SG and control rats after an oral gavage of glucose in the rats pretreated with the exendin (9-39) (Figure 4(e)), but these levels were significantly different when expressed as a percentage of baseline () (Figure 4(f)). These data indicate that GLP-1 reduced blood glucose by promoting insulin release.

(a)

(b)

(c)

(d)

(e)

(f)

3.5. SG Stimulates Jejunal and Ileal Villi Growth

Matching sections of jejunum and ileum were collected from the SG, PF-sham, and control rats at the end of the study to assess the effect of SG on intestinal morphology (Figure 5(a)). Increases in villus width in the jejunum and ileum were observed in the SG rats () (Figures 5(c) and 5(e)). There was a significant difference in the length of the jejunal villi between the control and SG rats () (Figure 5(b)), but the ileal villi length was not altered significantly () (Figure 5(d)). These data indicate that SG leads to a profound morphological adaptation in the jejunum and ileum.

(a)

(b)

(c)

(d)

(e)

3.6. SG Increases GLP-1 Expression Levels in the Jejunum and Ileum

We investigated GLP-1 protein expression, and preproglucagon and PCSK1 mRNA levels in the jejunum and ileum using immunohistochemistry and qRT-PCR, respectively, to determine the actions of SG in the jejunum and ileum in the GK rats. GLP-1 protein expression was significantly higher in the SG rats than in the PF-sham and control rats () (Figures 6(a), 6(b), and 6(e)). Preproglucagon and PCSK1 mRNA levels in the jejunum were not altered significantly in the SG rats compared with the control rats () (Figures 6(c) and 6(d)), but upregulated PCSK1 mRNA was observed in the ileum () (Figures 6(f) and 6(g)). Together, these data indicate that SG leads to increased GLP-1 expression in the mucosa of the jejunum and ileum.

(a)

(b)

(c)

(d)

(e)

(f)

(g)

4. Discussion

Recent studies have shown that medical therapy for obesity and comorbid T2DM is not as successful as bariatric surgery [20]. SG is gaining in popularity as an independent procedure because this approach is simple and effective in weight loss and resolves diabetes [21]. However, the underlying mechanisms of the metabolic benefits produced by SG remain largely unknown. This study investigated the effects of SG surgery on T2DM in GK rats. We found that SG increased postprandial GLP-1 levels, and insulin sensitivity, and the effect of improved glucose tolerance after SG was reversed by GLP-1 receptor antagonism. Notably, improvements in glucose metabolism were further supported by the increased expression of GLP-1 in the mucosa of jejunal and ileal tissues, which is consistent with the increased plasma GLP-1 level.

In the present work, we evaluated the effects of SG on body weight and food intake in GK diabetic rats. Our results showed that SG was effective in restraining body weight gain and reducing food intake of GK rats for the 18-week study duration. Basso et al. [22] reported that glandular gastrectomy, leaving the forestomach almost intact, did not induce significant body weight loss or reduced food intake from third week after surgery. The reason is that the aglandular stomach remains intact (the gastric section responsible for food storage and digestion in rat); this may permit normal food intake comparable to that of sham operation rats. Rodriguez et al. [23] have reported that a pair-fed group of rats had higher body weights and more adiposity than did a group of SG rats. However, no differences in body weight were observed between the PF-sham and SG-operated rats in our study. The food intake and body weight of the SG rats in our study were similar to those of the pair-fed rats in both the current study and a previous study [24], but we still detected a markedly reduced fasting glucose level in the SG rats. Although previous studies have demonstrated that glucose metabolism improves in association with weight loss after SG surgery [5, 25], other evidence support the ability of SG to elicit weight-independent changes to glucose homeostasis [22]. These results suggest that SG improves glucose metabolism, probably through weight-independent effects, in the GK rat model.

Our results demonstrated that the SG-treated rats exhibited better glucose and insulin tolerance than did the PF-sham rats with similar food intakes and body weights. This result is consistent with previous findings that SG ameliorates T2DM in GK rats more rapidly and effectively than does a greater restriction of food intake in matched nonoperated rats [26]. Clinical observations have demonstrated that low-calorie diets do not improve diabetes in obese patients who subsequently experience diabetes resolution from RYGB surgery [27]. Patients undergoing biliopancreatic diversion exhibit a temporary food intake reduction, but their eating capacity is restored or increases over time while their blood glucose levels remain under control [28]. SG may not just be a useful bariatric surgery; actually, there are differences in digestive and hormonal changes between SG and the traditional restrictive procedures, vertical banded gastroplasty and adjustable gastric banding (AGB). The hindgut hypothesis suggests that the early presentation of incompletely digested nutrients to the distal intestine after surgery leads to greater GLP-1 secretion from L-cells, subsequently improving insulin action [11]. In the SG rats, we observed a higher level of insulin excursion in the OGTT with the increase in GLP-1 level, but this effect was not observed in the IPIGTT. These results suggest that enhanced insulin release is driven by an enhanced incretin effect, such as that of GLP-1, rather than by the direct actions of circulating glucose on β-cells, which is consistent with the hindgut hypothesis. Clinical observations have demonstrated that post-SG hormonal changes occur even on the third postop day and before any food intake [29]. Peterli et al. [30] have found that postprandial plasma insulin is higher in RYGB patients than in SG patients one week postoperatively, but both surgery groups exhibit similar insulin levels at three months. Although there was a correlation between insulin sensitivity and body weight, the major driver of the improvement in insulin sensitivity after SG was GLP-1 secretion [31]. Changes in GLP-1 are often considered a mechanism for the weight-independent effects of bariatric surgery on glucose homeostasis, which may explain why purely restrictive procedures or nonsurgical weight loss have little effect on glucose control [32]. Gastaldelli et al. [33] studied obese patients without diabetes and demonstrated a difference in insulin sensitivity between the AGB and RYGB; specifically, they note an improvement in insulin sensitivity of adipose and muscle tissue in the RYGB. To assess the degree to which increased GLP-1 release in SG rats improved oral glucose tolerance, we also administered exendin (9-39) to block the GLP-1 receptor in the GK rats. We found that the majority of the incretin effect after SG was prevented by blocking GLP-1 receptors. Other studies have also demonstrated worse glucose control with GLP-1R blockade in rats after duodenojejunal exclusion, ileal translocation, and gastric bypass surgeries [5, 34, 35]. The clinical data also support the hypothesis that changes in the pattern of GLP-1 secretion mediate the effect of SG on diabetes [36]. Together, our results provide evidence that the improvement of glucose tolerance following SG surgery is mediated by enhanced GLP-1 action.

It is commonly believed that increased postprandial GLP-1 levels after RYGB are a result of gastrointestinal rearrangement, which produces a shortcut for undigested nutrients to enter the distal gut, thereby stimulating GLP-1-producing L-cells [5, 37]. However, the number of L-cells increases only in limbs that are exposed to undigested nutrients, the common and Roux limbs, but not the biliopancreatic limb, suggesting that the stimulation is a direct consequence of abnormal perfusion with undigested nutrients. SG does not involve a shortcut for nutrients, but similar increases in plasma GLP-1 levels have been observed [5]. The increases in intestinal villus length and width confirm the induction of adaptations, suggesting that there are significant effects of local nutrient contact in the stimulation of adaptations after SG in our study. Therefore, we further detected the protein expression levels of GLP-1 in the jejunal and ileal segments and found that the level of GLP-1 protein expression in the intestinal specimens was increased, which is consistent with the increased plasma GLP-1 level in the GK rats after SG. Wang et al. [38] have presented similar conclusions in the jejuno-ileal circuit procedure. We further investigated GLP-1-related gene and find that the preproglucagon and PCSK1 mRNA levels were increased in the ileal mucosa of the SG rats. Patriti et al. [12] indicated that good glycemic control, higher proglucagon mRNA expression has been shown to be present in the transposed ileal segment. We only examined PCSK1; therefore, we cannot rule out that other rate-limiting enzymes of GLP-1 were altered. Taken together, our results demonstrated that the level of GLP-1 expression not only in the ileal mucosa but potentially also in the jejunal mucosa was increased. These analyses suggest that SG resulted in stimulated intestinal villus growth and improved jejunal and/or ileal tissue expression of GLP-1, which is consistent with the increased plasma concentrations of GLP-1. The present study is, to our knowledge, the first report on the protein and mRNA expression levels of GLP-1 of the jejunal mucosa in SG procedure using the GK rat model. Gastric emptying after SG is accelerated for liquids or solids in the majority of obese patients [39]. Unfortunately, a cause-effect relationship between SG and gastric emptying was not confirmed in our study. However, other studies found that SG does not alter gastric emptying in obese patients [40, 41]. This result may have been due to differences in the size of the small pouch that impairs gastric emptying, differences in surgical technique, or a failure to distinguish between nondiabetics and diabetics in obese patients, given that diabetes may also affect gastrointestinal motility [42]. Understanding the role of SG in the GK rat model may provide further insight into surgically induced improvements in metabolism and may lead to the development of less invasive surgeries for obesity-related diabetes.

In conclusion, SG improved glucose metabolism, and insulin release was associated with increased GLP-1 secretion. SG contributes to an increase in plasma GLP-1 levels via increased GLP-1 expression in the mucosa of the jejunum and/or ileum. The effect of improved glucose tolerance after SG was reversed by GLP-1 receptor antagonism. This study provides evidence that the improvement of glucose metabolism following SG surgery is mediated by enhanced GLP-1 action.

Certain limitations must be considered in the interpretation of our results. First, a cause-effect relationship between SG and gastric emptying was not confirmed in our study. Second, our experiments used a nonobese GK rat model; future studies should utilize an obese model to obtain results more pertinent to human patient populations.

Additional Points

Animal Rights. All applicable institutional and/or national guidelines for the care and use of animals were followed.

Conflicts of Interest

All the authors declare that there are no conflicts of interest.

Acknowledgments

Support for these studies was provided by the National Basic Research Program of China (973 Program) (no. 2015CB554001, Jianping Wang), the National Natural Science Foundation of China (no. 81472257, Yanxin Luo; no. 81201920, Yanxin Luo; no. 81502022, Xiaolin Wang; no. 81672436, Yanxin Luo), the Natural Science Fund for Distinguished Young Scholars of Guangdong Province (no. 2016A030306002, Yanxin Luo), the Tip-top Scientific and Technical Innovative Youth Talents of Guangdong special support program (no. 2015TQ01R454, Yanxin Luo), the Natural Science Foundation of Guangdong Province (no. S2013010013607, Yanxin Luo; no. 2016A030310222, Huichuan Yu), the Science and Technology Program of Guangzhou (no. 201506010099, Yanxin Luo; no. 2014Y2-00160, Jianping Wang), the Fundamental Research Funds for the Central Universities (Sun Yat-sen University) (no. 2015ykzd10, Yanxin Luo; no. 13ykpy37, Yanxin Luo; no. 16ykpy35, Xiaolin Wang), and National Key Clinical Discipline.

References

B. Zhou, Y. Lu, K. Hajifathalian et al., “Worldwide trends in diabetes since 1980: a pooled analysis of 751 population-based studies with 4.4 million participants,” The Lancet, vol. 387, no. 10027, pp. 1513–1530, 2016.
View at: Publisher Site | Google Scholar
J. B. Dixon, C. W. le Roux, F. Rubino, and P. Zimmet, “Bariatric surgery for type 2 diabetes,” The Lancet, vol. 379, no. 9833, pp. 2300–2311, 2012.
View at: Publisher Site | Google Scholar
G. Mingrone, S. Panunzi, A. De Gaetano et al., “Bariatric surgery versus conventional medical therapy for type 2 diabetes,” The New England Journal of Medicine, vol. 366, no. 17, pp. 1577–1585, 2012.
View at: Publisher Site | Google Scholar
B. E. Bayham, F. L. Greenway, D. E. Bellanger, and C. E. O'Neil, “Early resolution of type 2 diabetes seen after Roux-en-Y gastric bypass and vertical sleeve gastrectomy,” Diabetes Technology & Therapeutics, vol. 14, no. 1, pp. 30–34, 2012.
View at: Publisher Site | Google Scholar
A. P. Chambers, L. Jessen, K. K. Ryan et al., “Weight-independent changes in blood glucose homeostasis after gastric bypass or vertical sleeve gastrectomy in rats,” Gastroenterology, vol. 141, no. 3, pp. 950–958, 2011.
View at: Publisher Site | Google Scholar
P. R. Schauer, S. R. Kashyap, K. Wolski et al., “Bariatric surgery versus intensive medical therapy in obese patients with diabetes,” The New England Journal of Medicine, vol. 366, no. 17, pp. 1567–1576, 2012.
View at: Publisher Site | Google Scholar
J. P. Regan, W. B. Inabnet, M. Gagner, and A. Pomp, “Early experience with two-stage laparoscopic Roux-en-Y gastric bypass as an alternative in the super-super obese patient,” Obesity Surgery, vol. 13, no. 6, pp. 861–864, 2003.
View at: Publisher Site | Google Scholar
M. Rizzello, F. Abbatini, G. Casella et al., “Early postoperative insulin-resistance changes after sleeve gastrectomy,” Obesity Surgery, vol. 20, no. 1, pp. 50–55, 2010.
View at: Publisher Site | Google Scholar
F. Rubino, M. Gagner, P. Gentileschi et al., “The early effect of the Roux-en-Y gastric bypass on hormones involved in body weight regulation and glucose metabolism,” Annals of Surgery, vol. 240, no. 2, pp. 236–242, 2004.
View at: Publisher Site | Google Scholar
K. Meirelles, T. Ahmed, D. M. Culnan, C. J. Lynch, C. H. Lang, and R. N. Cooney, “Mechanisms of glucose homeostasis after Roux-en-Y gastric bypass surgery in the obese, insulin-resistant Zucker rat,” Annals of Surgery, vol. 249, no. 2, pp. 277–285, 2009.
View at: Publisher Site | Google Scholar
P. C. Sala, R. S. Torrinhas, S. B. Heymsfield, and D. L. Waitzberg, “Type 2 diabetes mellitus: a possible surgically reversible intestinal dysfunction,” Obesity Surgery, vol. 22, no. 1, pp. 167–176, 2012.
View at: Publisher Site | Google Scholar
A. Patriti, M. C. Aisa, C. Annetti et al., “How the hindgut can cure type 2 diabetes. Ileal transposition improves glucose metabolism and beta-cell function in Goto-Kakizaki rats through an enhanced proglucagon gene expression and L-cell number,” Surgery, vol. 142, no. 1, pp. 74–85, 2007.
View at: Publisher Site | Google Scholar
J. J. Holst, “The physiology of glucagon-like peptide 1,” Physiological Reviews, vol. 87, no. 4, pp. 1409–1439, 2007.
View at: Publisher Site | Google Scholar
C. Orskov, L. Rabenhoj, A. Wettergren, H. Kofod, and J. J. Holst, “Tissue and plasma concentrations of amidated and glycine-extended glucagon-like peptide I in humans,” Diabetes, vol. 43, no. 4, pp. 535–539, 1994.
View at: Publisher Site | Google Scholar
X. Wei, X. Ma, R. Lu et al., “Genetic variants in PCSK1 gene are associated with the risk of coronary artery disease in type 2 diabetes in a Chinese Han population: a case control study,” PLoS One, vol. 9, no. 1, article e87168, 2014.
View at: Publisher Site | Google Scholar
L. L. Baggio and D. J. Drucker, “Biology of incretins: GLP-1 and GIP,” Gastroenterology, vol. 132, no. 6, pp. 2131–2157, 2007.
View at: Publisher Site | Google Scholar
D. J. Drucker, “The role of gut hormones in glucose homeostasis,” The Journal of Clinical Investigation, vol. 117, no. 1, pp. 24–32, 2007.
View at: Publisher Site | Google Scholar
J. J. Omana, S. Q. Nguyen, D. Herron, and S. Kini, “Comparison of comorbidity resolution and improvement between laparoscopic sleeve gastrectomy and laparoscopic adjustable gastric banding,” Surgical Endoscopy, vol. 24, no. 10, pp. 2513–2517, 2010.
View at: Publisher Site | Google Scholar
Y. Wang, L. Yan, Z. Jin, and X. Xin, “Effects of sleeve gastrectomy in neonatally streptozotocin-induced diabetic rats,” PLoS One, vol. 6, no. 1, article e16383, 2011.
View at: Publisher Site | Google Scholar
P. R. Schauer, D. L. Bhatt, J. P. Kirwan et al., “Bariatric surgery versus intensive medical therapy for diabetes—5-year outcomes,” The New England Journal of Medicine, vol. 376, no. 7, pp. 641–651, 2017.
View at: Publisher Site | Google Scholar
H. Buchwald and D. M. Oien, “Metabolic/bariatric surgery worldwide 2011,” Obesity Surgery, vol. 23, no. 4, pp. 427–436, 2013.
View at: Publisher Site | Google Scholar
N. Basso, E. Soricelli, L. Castagneto-Gissey et al., “Insulin resistance, microbiota, and fat distribution changes by a new model of vertical sleeve gastrectomy in obese rats,” Diabetes, vol. 65, no. 10, pp. 2990–3001, 2016.
View at: Publisher Site | Google Scholar
A. Rodriguez, S. Becerril, V. Valenti et al., “Short-term effects of sleeve gastrectomy and caloric restriction on blood pressure in diet-induced obese rats,” Obesity Surgery, vol. 22, no. 9, pp. 1481–1490, 2012.
View at: Publisher Site | Google Scholar
B. G. Bruinsma, K. Uygun, M. L. Yarmush, and N. Saeidi, “Surgical models of Roux-en-Y gastric bypass surgery and sleeve gastrectomy in rats and mice,” Nature Protocols, vol. 10, no. 3, pp. 495–507, 2015.
View at: Publisher Site | Google Scholar
D. M. Culnan, V. Albaugh, M. Sun, C. J. Lynch, C. H. Lang, and R. N. Cooney, “Ileal interposition improves glucose tolerance and insulin sensitivity in the obese Zucker rat,” American Journal of Physiology Gastrointestinal and Liver Physiology, vol. 299, no. 3, pp. G751–G760, 2010.
View at: Publisher Site | Google Scholar
Q. Wu, X. Zhang, M. Zhong et al., “Effects of bariatric surgery on serum bile acid composition and conjugation in a diabetic rat model,” Obesity Surgery, vol. 26, no. 10, pp. 2384–2392, 2016.
View at: Publisher Site | Google Scholar
J. Lima, L. Helena, S. Oliveira, L. Viana, and E. Godoy, “Rapid resolution of diabetes after gastric bypass,” Obesity Surgery, vol. 15, no. 3, pp. 448-449, 2005.
View at: Publisher Site | Google Scholar
N. Scopinaro, G. F. Adami, G. M. Marinari et al., “Biliopancreatic diversion,” World Journal of Surgery, vol. 22, no. 9, pp. 936–946, 1998.
View at: Publisher Site | Google Scholar
N. D. Basso, M. Capoccia, F. Rizzello et al., “First-phase insulin secretion, insulin sensitivity, ghrelin, GLP-1, and PYY changes 72 h after sleeve gastrectomy in obese diabetic patients: the gastric hypothesis,” Surgical Endoscopy, vol. 25, no. 11, pp. 3540–3550, 2011.
View at: Publisher Site | Google Scholar
R. Peterli, B. Wolnerhanssen, T. Peters et al., “Improvement in glucose metabolism after bariatric surgery: comparison of laparoscopic Roux-en-Y gastric bypass and laparoscopic sleeve gastrectomy: a prospective randomized trial,” Annals of Surgery, vol. 250, no. 2, pp. 234–241, 2009.
View at: Publisher Site | Google Scholar
G. E. Casella, L. Soricelli, A. Castagneto-Gissey, A. Redler, N. Basso, and G. Mingrone, “Changes in insulin sensitivity and secretion after sleeve gastrectomy,” The British Journal of Surgery, vol. 103, no. 3, pp. 242–248, 2016.
View at: Publisher Site | Google Scholar
W. Yan, D. Polidori, L. Yieh et al., “Effects of meal size on the release of GLP-1 and PYY after Roux-en-Y gastric bypass surgery in obese subjects with or without type 2 diabetes,” Obesity Surgery, vol. 24, no. 11, pp. 1969–1974, 2014.
View at: Publisher Site | Google Scholar
A. Gastaldelli, A. Iaconelli, M. Gaggini et al., “Short-term effects of laparoscopic adjustable gastric banding versus Roux-en-Y gastric bypass,” Diabetes Care, vol. 39, no. 11, pp. 1925–1931, 2016.
View at: Publisher Site | Google Scholar
S. Gaitonde, R. Kohli, and R. Seeley, “The role of the gut hormone GLP-1 in the metabolic improvements caused by ileal transposition,” The Journal of Surgical Research, vol. 178, no. 1, pp. 33–39, 2012.
View at: Publisher Site | Google Scholar
T. L. Kindel, S. M. Yoder, R. J. Seeley, D. A. D'Alessio, and P. Tso, “Duodenal-jejunal exclusion improves glucose tolerance in the diabetic, Goto-Kakizaki rat by a GLP-1 receptor-mediated mechanism,” Journal of Gastrointestinal Surgery, vol. 13, no. 10, pp. 1762–1772, 2009.
View at: Publisher Site | Google Scholar
S. Santoro, F. Q. Milleo, C. E. Malzoni et al., “Enterohormonal changes after digestive adaptation: five-year results of a surgical proposal to treat obesity and associated diseases,” Obesity Surgery, vol. 18, no. 1, pp. 17–26, 2008.
View at: Publisher Site | Google Scholar
N. Saeidi, L. Meoli, E. Nestoridi et al., “Reprogramming of intestinal glucose metabolism and glycemic control in rats after gastric bypass,” Science, vol. 341, no. 6144, pp. 406–410, 2013.
View at: Publisher Site | Google Scholar
Y. Wang, X. Zhang, M. Zhong et al., “Improvements of glucose and lipid metabolism after jejuno-ileal circuit procedure in a non-obese diabetic rat model,” Obesity Surgery, vol. 26, no. 8, pp. 1768–1776, 2016.
View at: Publisher Site | Google Scholar
I. Braghetto, C. Davanzo, O. Korn et al., “Scintigraphic evaluation of gastric emptying in obese patients submitted to sleeve gastrectomy compared to normal subjects,” Obesity Surgery, vol. 19, no. 11, pp. 1515–1521, 2009.
View at: Publisher Site | Google Scholar
H. Bernstine, R. Tzioni-Yehoshua, D. Groshar et al., “Gastric emptying is not affected by sleeve gastrectomy–scintigraphic evaluation of gastric emptying after sleeve gastrectomy without removal of the gastric antrum,” Obesity Surgery, vol. 19, no. 3, pp. 293–298, 2009.
View at: Publisher Site | Google Scholar
S. Shah, P. Shah, J. Todkar, M. Gagner, S. Sonar, and S. Solav, “Prospective controlled study of effect of laparoscopic sleeve gastrectomy on small bowel transit time and gastric emptying half-time in morbidly obese patients with type 2 diabetes mellitus,” Surgery for Obesity and Related Diseases, vol. 6, no. 2, pp. 152–157, 2010.
View at: Publisher Site | Google Scholar
S. S. Yarandi and S. Srinivasan, “Diabetic gastrointestinal motility disorders and the role of enteric nervous system: current status and future directions,” Neurogastroenterology & Motility, vol. 26, no. 5, pp. 611–624, 2014.
View at: Publisher Site | Google Scholar

Copyright

Copyright © 2018 Laiyuan Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

PDF Download Citation

Download other formats

Order printed copies

Views

3559

Downloads

1183

Citations