A Protocol for Roux-en-Y Gastric Bypass in Rats using Linear Staplers

Podsumowanie

Roux-en-Y gastric bypass (RYGB) is performed to treat obesity and diabetes. However, the mechanisms underlying RYGB's efficacy are not fully understood, and studies are limited by technical difficulty leading to high mortality in animal models. This article provides instructions on how to perform RYGB in rats with high success rates.

Streszczenie

Roux-en-Y gastric bypass (RYGB) is commonly performed for the treatment of severe obesity and type 2 diabetes. However, the mechanism of weight loss and metabolic changes are not well understood. Multiple factors are thought to play a role, including reduced caloric intake, decreased nutrient absorption, increased satiety, the release of satiety-promoting hormones, shifts in bile acid metabolism, and alterations in the gut microbiota.

The rat RYGB model presents an ideal framework to study these mechanisms. Prior work on mouse models have had high mortality rates, ranging from 17 to 52%, limiting their adoption. Rat models demonstrate more physiologic reserve to surgical stimulus and are technically easier to adopt as they allow for the use of surgical staplers. One challenge with surgical staplers, however, is that they often leave a large gastric pouch which is not representative of RYGB in humans.

In this protocol, we present a RYGB protocol in rats that result in a small gastric pouch using surgical staplers. Utilizing two stapler fires which remove the forestomach of the rat, we obtain a smaller gastric pouch similar to that following a typical human RYGB. Surgical stapling also results in better hemostasis than sharp division. Additionally, the forestomach of the rat does not contain any glands and its removal should not alter the physiology of RYGB.

Weight loss and metabolic changes in the RYGB cohort were significant compared to the sham cohort, with significantly lower glucose tolerance at 14 weeks. Furthermore, this protocol has an excellent survival of 88.9% after RYGB. The skills described in this protocol can be acquired without previous microsurgical experience. Once mastered, this procedure will provide a reproducible tool for studying the mechanisms and effects of RYGB.

Wprowadzenie

Obesity and type 2 diabetes have become worldwide epidemics¹. Although medical weight loss can improve diabetes in patients, those with severe diabetes benefit most from bariatric surgery. Bariatric surgery has proven to be safe and effective at weight loss and improving or curing type 2 diabetes^2,3, even in those with long-standing disease⁴. Metabolic bariatric procedures, such as the current gold-standard Roux-en-Y gastric bypass (RYGB) surgery, induce rapid and sustained improvements in glucose homeostasis while also reducing the need for diabetic medications^5,6,7.

After RYGB, glucose homeostasis improvement occurs rapidly and is independent of the weight loss⁸. Two major theories have been proposed to explain the metabolic changes associated with diabetes remission that occur following metabolic surgery. First, the hindgut hypothesis postulates that, after bypass, higher concentrations of undigested nutrients reach the distal intestine enhancing the release of hormones such as GLP-1. On the other hand, the foregut hypothesis suggests that bypassing the proximal intestine reduces the secretion of anti-incretin hormones. Both of these effects could lead to early improvement of glucose metabolism⁹.

Animal models have the potential to be a powerful tool to study these mechanisms. However, a major barrier in utilizing mouse or rat models is the technical difficulty in performing these procedures. Most studies have relied on mouse or rat models^10,11,12. Mouse models have been difficult as the mouse stomach is too small to use stapler devices¹¹, and mortality rates are unacceptably high, ranging from 17 to 52%¹³. In rats, some protocols remain technically difficult to perform due to complex ligation of gastric vessels prior to dividing the stomach^12,14. Other models divide the stomach using a stapler but leave a large pouch not consistent with the post RYGB human anatomy¹¹. In this model, we provide detailed instructions on how to perform RYGB using linear staplers in a rat model resulting in a gastric pouch more in keeping with that of human anatomy. Overall, this procedure was associated with excellent survival rates and metabolic outcomes.

Protokół

Animal use protocols were approved by the Health Science Animal Care and Use Committee at the University of Alberta (AUP00003000). See Figure 1 for a diagram demonstrating the RYGB anatomy.

1. Roux-en-Y gastric bypass

1. Preparation of animals and operative setup
   1. One week prior to the surgery, provide the rats with oral rehydration therapy and liquid diet in addition to their solid diet and water to acclimatize them to this new diet.
   2. Fast rats with only access to water for 12-18 h prior to the surgery.
      1. Ensure rats are fasted on a raised wire platform so that they cannot consume bedding material.
   3. Inject rats with subcutaneous long buprenorphine sustained release (SR) at a dose of 1 mg/kg immediately before surgery.
   4. Autoclave all surgical instruments, towels, and drapes.
   5. Clean the operating surface, heating pad, and anesthetic nose cone with 70% ethanol.
   6. Set up the operating surface with an operating microscope, anesthetic machine, and supplies in a manner that is ergonomic for the operating surgeon.
   7. Use a temperature-regulated heating pad and set to 37 °C.
   8. Place a sterile drape or towel over the heating pad.
   9. Fill a 50 mL sterile conical tube with 0.9% saline.
2. Anesthetic induction and preparation
   1. Induce anesthesia using 4% isoflurane as per previously established protocols¹⁵.
   2. Apply pressure to the hindfoot of all four limbs to ensure there is no pain response.
   3. Check for adequate anesthesia and respiratory rate after every 5 min.
   4. Apply lubricant to both eyes to prevent drying.
   5. Shave hair from the abdomen.
   6. Clean the abdomen with a povidone-iodine solution. Allow the solution to dry, and change into sterile gloves.
   7. Drape the rat with an opening in the drape to expose the abdomen.
   8. Place instruments, sutures, cotton swabs, and a 10 mL syringe in a location that permits easy access during the procedure.
3. Median laparotomy
   1. Make a 3 cm incision in the upper midline of the abdomen using a scalpel, just below the xyphoid process as a landmark.
   2. Using scissors, divide the fascia and peritoneum, with care to stay midline on the linea alba to reduce bleeding from the rectus abdominus. If there is bleeding, control it with thermal or electrocautery.
4. Mobilizing the stomach
   1. Using two wet cotton swabs, bluntly dissect gastric attachments.
   2. When encountering dense adhesions, use thermal cautery to divide gastric attachments with care to avoid cauterizing the stomach. Sharply divide the ligament between the stomach and the accessory liver lobe to reduce the risk of liver tearing with stomach mobilization.
   3. For larger blood vessels, especially at the short gastric arteries, ligate using 6-0 polypropylene suture.
   4. Create a window on the right distal side of the esophagus but proximal to the left gastric artery. Ensure that a cotton swab can reach into this area posteriorly. The stomach is adequately mobilized when it can be exteriorized outside of the abdomen.
5. Identify and divide the jejunum
   1. Identify the ligament of Treitz by following the jejunum proximally until observing it is attachment to the transverse mesocolon.
   2. Measure 7 cm distally, identify a location between mesenteric vessels, and divide the bowel with micro scissors. Avoid Peyer's patches when dividing the bowel. Take care to only divide the bowel and not the mesentery.
   3. Place a clean, saline soaked sponge prior to dividing the bowel to minimize contamination.
   4. Check for the presence of a small crossing vessel in the mesentery at the border of the small bowel and divide this with cautery to avoid bleeding.
   5. Continue to divide the mesentery 1 cm towards the mesenteric base.
   6. Identify the proximal and distal jejunum. Place the proximal jejunum under a wet gauze on the rat's right and the distal jejunum on the rat's left.
6. Stapling the stomach
   1. Insert a 45 mm linear cutting stapler with 3.5 mm staple height across the white line of the forestomach to create a smaller pouch. Wait for 10 s before firing the stapler.
   2. Place pressure using gauze on the staple lines for 1 min to ensure hemostasis. If hemostasis is not achieved with pressure alone, bleeding along the staple line is oversewn using 6-0 polypropylene figure of eight sutures.
   3. Perform a second staple fire across the stomach into the window created previously. Wait for 10 s before firing the stapler. Pressure is held along the staple line to ensure hemostasis, and oversewing may be needed.
7. Gastrojejunostomy
   1. Make a gastrotomy immediately after stapling the stomach. Delays in this can cause gastric distension and aspiration as the stomach is discontinuous after the second gastric staple.
   2. Using an 11-blade scalpel, create a gastrotomy at the distal pouch. Express gastric contents through the gastrotomy. This is important to prevent gastric distension and aspiration. Lengthen this gastrotomy using micro scissors to approximately 5 mm. The gastrotomy is made large enough for the cotton swab tip just to fit through.
   3. Mobilize the distal end of the jejunum adjacent to the gastrotomy and place such that the mesentery is not twisted.
   4. While suturing the anastomosis, ensure that the bowel is kept moist by covering it with saline-soaked gauze and reapplying saline regularly.
   5. Using 6-0 polydioxanone or polypropylene suture, place a stay suture at the inferior margin of the anastomosis and gently retract using a snap. Tie with three knots.
   6. Place a stay suture at the superior margin of the anastomosis and gently retract using a snap. Tie with six knots.
   7. Suture the anterior side of the anastomosis in a continuous fashion, taking bites 1 mm wide and 1 mm apart with care to avoid taking the backside.
   8. Once the suture has reached the inferior stay suture, tie these together with an additional six knots.
   9. Once the anterior side is complete, flip the bowel and stomach over and pass the inferior stay suture through the mesenteric defect. Reapply the snap and retract inferiorly.
   10. For the posterior side of the anastomosis, place full thickness interrupted 6-0 sutures, 1 mm wide, and spaced 1 mm apart, with care to avoid taking the backside. These are tied with six knots each.
       NOTE: The anterior side of the anastomosis is sutured in a continuous fashion while the posterior side is done in an interrupted fashion. This prevents potential stricture or stenosis associated with a continuous circumferential closure.
   11. Check for the leakage by gently pushing luminal contents across the anastomosis. If there are areas with leakage, carefully reinforce them with interrupted sutures. Take care to avoid taking the backwall when reinforcing with extra sutures.
8. Jejunojejunostomy
   1. From the gastrojejunostomy, measure 20 cm distally.
   2. Create a jejunotomy on the antimesenteric side using the 11-blade scalpel. Avoid making the jejunotomy over Peyer's patches.
   3. Extend this jejunotomy using micro scissors, such that it is the same size as the biliopancreatic limb. Ensure that a cotton swab just fits inside.
   4. Place the biliopancreatic limb such that there is no twisting of the mesentery.
   5. Perform the anastomosis similarly to the gastrojejunostomy with 6-0 stay sutures on the superior and inferior sides. The anterior side is performed with continuous sutures while the posterior side is performed with interrupted sutures.
   6. Ensure that the bowel is kept moist with saline during this anastomosis.
   7. Check for leakage by gently pushing luminal contents through the anastomosis. If there are areas with leakage, reinforce them with interrupted sutures.
9. Reposition the bowel and stomach
   1. Ensure that there is no twisting of the pouch, remnant stomach, or liver. Ensure that the left lobe of the liver is anterior to the stomach and not trapped behind the pouch as this can cause compressive liver ischemia.
   2. Position the bowel in the abdomen in its natural position such that there is no twisting.
10. Abdominal closure
    1. Close the fascia with 3-0 polyglactin in a continuous fashion. 3-0 polydioxanone may also be used.
    2. Close the skin with 2-0 silk in a continuous fashion.
11. Anesthetic emergence
    1. Decrease isoflurane to zero but continue supplemental oxygen.
    2. Administer a local anesthetic as a splash block to the incision.
    3. Administer 10 mL of subcutaneous 5% dextrose in normal saline (D5NS) in the subcutaneous tissue behind the neck.
    4. Place an Elizabethan rat collar before the rat is fully awake. Take care to fit it snugly but not too tight to cause discomfort.
       ​NOTE: The collar is kept on until day 5 to prevent wound dehiscence.

2. Sham surgery

NOTE: Sham surgery is performed similar to RYGB, however, no anastomoses are performed.

1. A gastrotomy is created and then closed with 6-0 polydioxanone or polypropylene sutures.
2. A jejunotomy is created 7 cm distal to the ligament of Treitz and then closed with 6-0 polydioxanone or polypropylene sutures.

3. Postoperative care

1. Postoperative care
   1. House rats individually and keep them on raised wire platforms until solid food is reintroduced to prevent consumption of bedding and luminal obstruction.
      NOTE: Postoperative diet is resumed gradually as edema at the gastrojejunostomy can cause obstruction with the early resumption of solid diet.
   2. Inspect the feet daily while rats are on raised wire platforms for any skin changes.
   3. Keep rats on water and oral rehydration therapy diet for the first 72 h.
   4. Administer 10 mL of D5NS every 12 h for the first 72 h.
   5. Administer subcutaneous short-acting buprenorphine at 0.01 mg/kg if rats appear to be in pain. The Rat Grimace Scale is used to assess for pain¹⁶.
   6. On postoperative day 3, add rodent liquid diet. Continue to provide water and oral rehydration therapy.
   7. On postoperative day 5, restart high-fat diet. Continue to provide water and liquid diet. Remove the Elizabethan collar.
   8. On postoperative day 7, discontinue liquid diet.
   9. Remove skin sutures on postoperative day 10-14.

Wyniki

Animals and housing
36 male Wistar rats were housed in pairs and were fed 60% sterile rodent high-fat diet starting from six weeks of age (Figure 2). At 16 weeks of age, they underwent RYGB or sham surgery. After the first postoperative week, rats were resumed on a high fat diet. Half of the rats were euthanized at 2 weeks post-operative and the other half were euthanized at 14 weeks postoperative.

Mortality
Overall, 3...

Dyskusje

RYGB involves the creation of a small gastric pouch (less than 30 mL), and the creation of a biliopancreatic limb and a Roux limb (Figure 1). In humans, the biliopancreatic limb is typically 30 to 50 cm and transports secretions from the gastric remnant, liver, and pancreas. The Roux limb is typically 75 to 150 cm in length and is the primary channel for ingested food. The common channel is the remaining small bowel distal to where the two limbs join and is where the majority of digestion an...

Materiały

Name	Company	Catalog Number	Comments
2-0 Silk Sutures	Ethicon	K533
3-0 Vicryl Sutures	Ethicon	J219H
4% Isoflurane	N/A	N/A
5% Dextrose and 0.9% Sodium Chloride Solution - 1000 mL	Baxter	2B1064
50 mL Conical Centrifuge Tubes	Fisher Scientific	14-432-22
6-0 Prolene Sutures	Ethicon	8805H
Anesthetic Machine	N/A	N/A
Animal Hair Shaver	N/A	N/A
Betadine Solution	N/A	N/A
Castrojievo Needle Holder with lock 14 cm (smooth curved)	World Precision Instruments	503258
ECHELON FLEX Articulating Endoscopic Linear Cutter	Ethicon	EC45A
Economy Tweezers #4	World Precision Instruments	501978
ENDOPATH ETS Articulating Linear Cutter 45mm Reloads	Ethicon	6R45B
Far Infrared Warming Pad Controller with warming pad (15.2 cm W x 20.3 cm L), pad temperature probe, and 10 disposable, non-sterile sleeve protectors	Kent Scientific	RT-0515
Large Rat Elizabethan Collar	Kent Scientific	EC404VL-10
Liquid Diet Feeding Tube (150 mL)	Bio-Serv	9007
Liquid Diet Feeding Tube Holder (short adjustable)	Bio-Serv	9015
Micro Mosquito Forceps	World Precision Instruments	500452
Micro Scissors	World Precision Instruments	503365
Mouse Diet, High Fat Fat Calories (60%), Soft Pellets	Bio-Serv	S3282
No. 11 Blade and Scalpel Handle	N/A	N/A
OPMI Vario Surgical Microscope	ZEISS	S88
Raised Floor Grid	Tecniplast	GM500150 Raised Floor Grid
Rodent Liquid Diet, Lieber-DeCarli '82, Control, 4 Liters/Bag	Bio-Serv	F1259
Sodium Chloride Irrigation 0.9% Solution - 500 mL	Baxter	JF7633
Sterile Cotton Swabs	N/A	N/A
Sterile Drape	N/A	N/A
Sterile Towel	N/A	N/A
Thermal Cautery Unit	World Precision Instruments	501293