Using Multi-fluorinated Bile Acids and In Vivo Magnetic Resonance Imaging to Measure Bile Acid Transport

Podsumowanie

Tools to diagnose bile acid malabsorption and measure bile acid transport in vivo are limited. An innovative approach in live animals is described that utilizes combined proton (¹H) plus fluorine (¹⁹F) magnetic resonance imaging; this novel methodology has translational potential to screen for bile acid malabsorption in clinical practice.

Streszczenie

Along with their traditional role as detergents that facilitate fat absorption, emerging literature indicates that bile acids are potent signaling molecules that affect multiple organs; they modulate gut motility and hormone production, and alter vascular tone, glucose metabolism, lipid metabolism, and energy utilization. Changes in fecal bile acids may alter the gut microbiome and promote colon pathology including cholerrheic diarrhea and colon cancer. Key regulators of fecal bile acid composition are the small intestinal Apical Sodium-dependent Bile Acid Transporter (ASBT) and fibroblast growth factor-19 (FGF19). Reduced expression and function of ASBT decreases intestinal bile acid up-take. Moreover, in vitro data suggest that some FDA-approved drugs inhibit ASBT function. Deficient FGF19 release increases hepatic bile acid synthesis and release into the intestines to levels that overwhelm ASBT. Either ASBT dysfunction or FGF19 deficiency increases fecal bile acids and may cause chronic diarrhea and promote colon neoplasia. Regrettably, tools to measure bile acid malabsorption and the actions of drugs on bile acid transport in vivo are limited. To understand the complex actions of bile acids, techniques are required that permit simultaneous monitoring of bile acids in the gut and metabolic tissues. This led us to conceive an innovative method to measure bile acid transport in live animals using a combination of proton (¹H) and fluorine (¹⁹F) magnetic resonance imaging (MRI). Novel tracers for fluorine (¹⁹F)-based live animal MRI were created and tested, both in vitro and in vivo. Strengths of this approach include the lack of exposure to ionizing radiation and translational potential for clinical research and practice.

Wprowadzenie

Along with their classical role as detergents that facilitate fat absorption from the gut, bile acids have emerged as potent signaling molecules affecting multiple organs in addition to those associated with their enterohepatic circulation^1,2. In addition to controlling their own metabolism, bile acids modulate several aspects of gastrointestinal physiology (e.g., gut motility and incretin hormone production, colon physiology, and cancer susceptibility) and have systemic effects on vascular tone, glucose and lipid metabolism, and energy utilization. While some of these effects are mediated in the gut, others are due to postprandial changes in systemic bile acid levels, as noted in obese patients or after gastric by-pass surgery. To elucidate the complex metabolic actions of bile acids new technology is required that permits simultaneous monitoring of bile acid levels in different anatomical compartments, in the gastrointestinal tract and metabolic tissues (liver, pancreas, skeletal muscle and adipose). Obtaining such temporal and spatial information requires innovative technology - in vivo imaging using novel bile acid tracers as described here is such a novel approach.

Bile acid composition and distribution in anatomical compartments are regulated by factors that modulate their hepatic synthesis and ileal uptake, including diet, surgery, antibiotic use and changes in gut flora. A key regulator of intestinal bile acid uptake for their enterohepatic circulation³ (Figure 1) is the ileal Apical Sodium-dependent Bile Acid Transporter (ASBT; SLC10A2). Although passive absorption occurs throughout the intestines, ASBT mediates uptake of 95% of intestinal bile acids so that normally there is limited spillage of bile acids into the feces. Asbt-deficient (Slc10a2^-/-) mice have increased fecal bile acids and a diminished bile acid pool⁴.

Figure 1: Enterohepatic Circulation of Bile Acids.
Illustration of Enterohepatic Circulation whereby Bile Acids are Synthesized in the Liver, Excreted into the Biliary Tree, Stored in the Gallbladder, Released into the Proximal Small Intestine with Meals, and Actively taken up via ASBT in the Distal Ileum. Whereas small amounts of bile acids are absorbed passively throughout the gut, approximately 95% of intestinal bile acids are transported actively by ASBT resulting in minimal (approximately 5%) loss in the stool which is compensated by a similar amount of new bile acid synthesis in the liver, thereby maintaining a steady-state bile acid pool. The arrows on the right identify factors that may impact native and fluorine-labeled bile acid stability, including gastric acid, pancreatic and intestinal mucosal enzymes, and, most importantly, hydrolytic enzymes released by Clostridial species that colonize the distal small bowel and colon. (Modified with permission¹⁶) Please click here to view a larger version of this figure.

Bile acid malabsorption can be categorized into three types, each of which increases fecal dihydroxy bile acids, thereby causing intermittent or chronic diarrhea. Type 1 results from gross ileal pathology (e.g., resection, Crohn disease)⁵. Type 3 results from cholecystectomy, vagotomy, celiac disease, bacterial overgrowth, and pancreatic insufficiency. In contrast, persons with 'primary' (Type 2) bile acid malabsorption pose a formidable diagnostic challenge because they lack such antecedent conditions and do not have evidence of pathology in the ileum. Hence, primary bile acid malabsorption is commonly misdiagnosed as diarrhea-predominant irritable bowel syndrome (IBS-D), perhaps the most common reason for gastroenterology-related out-patient visits. It has been estimated that one-third of patients with IBS-D have primary bile acid malabsorption; in the U.S., this may represent several million persons⁵. Recent insights indicate that primary BAM derives from impaired feedback inhibition of hepatic bile acid synthesis by intestinal fibroblast growth factor-19 (FGF19), not from reduced expression or function of ASBT.

In primary bile acid malabsorption, low plasma levels of FGF19 fail to shut off hepatic bile acid synthesis - the resulting increase in intestinal bile acids saturates bile acid transporters, including ASBT, and the augmented spillage of bile acids into the feces causes diarrhea⁶ (Figure 2). Mice deficient in Fgf15 (murine FGF19) have an expanded bile acid pool and increased fecal bile acids⁷.

Figure 2: Mechanisms of Intestinal Bile Acid Malabsorption.
Normally, as shown in panel A, approximately 95% of intestinal bile acids are absorbed by active transport in the distal ileum via ASBT. When ASBT expression or activity is diminished (panel B), impaired intestinal bile acid uptake results in spillage of bile acids into the colon. With impaired FGF19 signaling (panel C), the lack of feedback inhibition of hepatic bile acid synthesis results in increased concentrations of intestinal bile acids that overwhelm ASBT transport capacity with spillage of bile acids into the colon. Please click here to view a larger version of this figure.

Long-term, chronic elevation in fecal bile acids may promote colon neoplasia. Colon neoplasia arises from progressive mucosal dysplasia associated with somatic gene mutations, but environmental factors that increase fecal bile acids may accelerate and augment this process. In rodents, increased fecal bile acids either as a consequence of exogenous administration or Asbt deficiency promote colon dysplasia and tumor formation^8-10.

Notably, provocative findings indicate that commonly-used drugs approved by the Food and Drug Administration (FDA) potently inhibit bile acid transport by ASBT in vitro¹¹. If these drugs reduce small intestinal bile acid transport in vivo and increase fecal bile acid levels, the potential impact on colon pathology would be concerning. Even a small increase in colon pathology attributed to use of such a drug could have a major health impact. A toolkit which can assess the plausibility of these in vitro findings and epidemiologic observations would spur additional research, including post-marketing safety studies.

Despite the need, practical assays to identify people with bile acid malabsorption are lacking. Direct measurement of fecal bile acids was rejected years ago as cumbersome, impractical, and unreliable⁵. Alternative approaches include measuring retention of a radioactive selenium-labeled cholic acid derivative (⁷⁵SeHCAT) and plasma levels of 7α-hydroxy-4-cholesten-3-one (C4), or a therapeutic trial of bile acid binders. ⁷⁵SeHCAT testing has limited availability in Europe and is not FDA-approved or available for use in the U.S. Moreover, even modest radiation exposure (0.26 mSv/⁷⁵SeHCAT test) from diagnostic testing raises concerns, and bacterial overgrowth and advanced liver disease may confound ⁷⁵SeHCAT results. C4 testing is potentially attractive since only plasma is required, but it has low positive-predictive value and testing is not widely available. Measuring serum levels of FGF19 has similar limitations. Frequently clinicians resort to a therapeutic trial of bile acid sequestrants, but this approach cannot provide a definitive diagnosis of bile acid malabsorption⁵.

For these reasons, a novel MRI approach was conceived to measure bile acid transport and distribution in vivo using innovative multi-fluorinated bile acids (MFBA-MRI). MFBA containing three atoms of fluorine (¹⁹F), a stable isotope of 100% natural abundance, are transported similarly to native bile acids¹², and can be used to visualize bile acid transport with a combination of proton (¹H) and fluorine (¹⁹F) MRI, a sensitive, safe method without ionizing radiation exposure^13,14.

Protokół

The following protocol adheres to guidelines approved by the Institutional Animal Care and Use Committee (IACUC) at the University of Maryland School of Medicine (IACUC Protocol #0415011, approved June 18, 2015).

1. Gavaging Mice with ¹⁹F-Labeled Bile Acids

1. Gavage mice with 150 mg/kg body weight ¹⁹F-labeled bile acids. Fill a 1-ml syringe to the necessary volume with ¹⁹F-labeled bile acid stock solution [cholic acid-trifluoro-acetyl lysine (CA-lys-TFA; in 1:1 polyethylene glycol 400:Dulbecco's phosphate buffered saline) or cholylsarcosine-trifluoro-N-methyl-acetamide (CA-sar-TFMA; in 60% polyethylene glycol 400 and 40% Dulbecco's phosphate buffered saline] and attach a 20-gauge 1.5-inch curved bulb-tipped gastric gavage needle. Make sure the gavage needle is long enough to reach the level of the mouse’s xyphoid cartilage when inserted in the esophagus up to the hub of the needle
2. Firmly grasp the animal by the loose skin at the back of the neck between the thumb and index finger and use the remaining fingers to grasp the skin on the lower back and tail.
3. Hold the mouse upright and pass the gavage needle along the side and the roof of the mouth into the esophagus and down into the stomach. If resistance is encountered at the pharynx, reposition the needle until the animal 'swallows' it — do not push against resistance.
4. If anesthesia is required for gavage, place the mouse in a bell jar containing 5 ml isoflurane and close. When the mouse falls on its side, wait 7 sec, remove the mouse and perform gavage. To protect personnel from anesthetic vapors, use the bell jar only in a fume hood.
5. Observe the animal recover from isoflurane in a few min.
   NOTE: Since isoflurane is metabolized by the liver, a fluorine signal emanating from intact drug or its metabolites excreted into the biliary system and gallbladder can confound fluorine signals from ¹⁹F-labeled bile acids¹⁵. An alternative is to use ketamine plus xylazine (see section 3.1 for doses).

2. Harvesting the Gallbladder, the Liver and Blood for Bile Acid Measurements Using Liquid Chromatography/Mass Spectrometry

1. To achieve maximal gallbladder filling, fast mice for at least 6 hr before harvesting the organs. Prepare ketamine and xylazine in phosphate-buffered saline (100 µl ketamine, 62.5 µl xylazine, 840 µl PBS).
2. Using a 1-ml sterile syringe, inject a mouse subcutaneously 1 hr prior to organ harvest with 15 µl/g body weight of ketamine/xylazine solution (150 mg ketamine and 18 mg xylazine per kg body weight).
3. One hr after administering ketamine/xylazine confirm adequate anesthesia by toe pinch and place the anesthetized mouse supine.
4. Use 5 or 6 inch scissors to make a midline abdominal skin incision from the pubis to the xyphoid and fine scissors (4 inch) to cut the peritoneal lining and expose abdominal organs — do not to pierce the diaphragm.
5. Grasp the xyphoid process with a 5 inch clamp and lift back across the chest to expose the upper abdominal cavity. Use forceps and a blunt instrument to dissect and move the liver aside, exposing the gallbladder.
   NOTE: Do not lacerate the liver or touch the gallbladder as the former will cause severe bleeding and the latter may stimulate gallbladder contraction and emptying.
6. Place a 4-inch clamp across the common bile duct (Figure 3, dashed arrows). Cut the ligament attaching the superior pole of the gallbladder to the diaphragm and gently move the gallbladder to the right side of the abdomen.

Figure 3: Anatomical and Proton MRI Views of the Mouse Gallbladder.
The left panel shows the exposed mouse gallbladder to the left of midline after abdominal incision. The clamp grasps the xyphoid process. The bile-filled fasting gallbladder is indicated by the large arrow and the clamped common bile duct by the dashed arrows. [Inset: Excised intact gallbladder with the common bile duct clamped. The ruler is marked in millimeters (mm).] The right panel shows a high-resolution proton density-weighted MRI image of the fasting murine gallbladder (arrow). Please click here to view a larger version of this figure.

7. Before excising the gallbladder perform cardiac puncture, harvest blood, and exsanguinate the animal to verify euthanasia.
   ​NOTE: Harvesting the gallbladder first may lacerate the liver causing cardiovascular collapse and failure to obtain an adequate blood sample (≥ 200 µl).
8. Expose the underside of the left diaphragm and identify the beating surface of the heart. At the point of maximal cardiac pulsation puncture the diaphragm and heart with a 23-gauge needle attached to a 1-ml syringe.
   1. Slowly withdraw the syringe while aspirating. When blood starts to fill the syringe, stop withdrawing and maintain suction to collect 0.2 - 0.6 ml blood. Gently rotating the needle or withdrawing it slightly may re-establish flow if it ceases.
   2. Transfer the blood to a 1.5-ml heparinized tube and centrifuge at 2,000 x g for 15 min. Precipitate the plasma with four parts acetonitrile and centrifuge at 12,000 x g for 10 min. Analyze the supernatant by liquid chromatography/mass spectroscopy (LC/MS/MS)^{11-1312-1412-1412-1412-14}. If necessary, store the plasma at -80 ^oC before analysis.
9. Using blunt dissection, free the gallbladder from the liver. Transect the common bile duct below the clamp, remove and weigh the gallbladder, and place it in a 1.5-ml microcentrifuge tube. Harvest the liver.
10. Homogenize approximately 100 mg of liver and the entire gallbladder on ice in a size-21 glass tissue homogenizer. Extract with 75% acetonitrile and 25% water (800 µl for liver, 300 µl for gallbladder) and centrifuge at 12,000 x g for 10 min. Dilute extracts as necessary and quantify bile acid contents using LC/MS/MS^11-13.

3. Live Animal Proton (¹H) and Fluorine (¹⁹F) Magnetic Resonance Imaging

1. To achieve maximal gallbladder filling, fast mice for at least 6 hr before imaging. Using ketamine and xylazine, anesthetize mice to prevent motion in the MRI scanner. Prepare a stock solution of ketamine plus xylazine in phosphate buffered saline (130 µl ketamine, 42.5 µl xylazine, 827 µl PBS). One hr before MRI, use a 1-ml sterile syringe to inject a mouse subcutaneously with 5 µl/g body weight of this solution (65 mg ketamine and 4.25 mg xylazine per kg body weight). To prevent dryness under anesthesia apply veterinary ointment to the animal's eyes.
2. After induction with ketamine/xylazine as above, clip a 1.5 cm² area on left lower half of the mouse abdomen using #40 or finer electric clipper blades. After fur removal, prep the area with 8 - 12% diluted iodine surgical scrub solution and rinse with 70% alcohol — repeat both steps. Insert a 24-gauge by 0.75-inch needle/catheter subcutaneously and tunnel into the abdominal cavity. Make sure the catheter is not in the cecum or other abdominal organ by pulling back on the plunger — there should be no blood or fecal material in the catheter.
3. Remove the needle and leave the intraperitoneal catheter. Place the mouse on a temperature-controlled thermal pad in the MRI scanner animal chamber.
4. Prepare a 1-ml sterile syringe containing ketamine and xylazine in phosphate buffered saline (1,000 µl ketamine, 300 µl xylazine, 6,700 µl PBS) and fill the desired length of 72-inch sterile tubing. Connect the intraperitoneal catheter to the prefilled sterile tubing and extend it away from the MRI scanner. To maintain anesthesia inject 50 µl of this solution every 20 min if the mouse’s vital signs are stable.
   ​NOTE: Before imaging, make certain no metals are near the MRI scanner.
5. Use a ¹⁹F/¹H dual-tuned linear volume MRI coil to transmit and receive radio frequency signals at 300.283 MHz for ¹H and 282.524 MHz for ¹⁹F nuclei.
   1. Perform system calibration^{11, 13} and animal localization with three-slice (axial, mid-sagittal, and coronal) scout images using a fast low-angle shot sequence (FLASH). To start the experiment, click the 'traffic light' button in the Scan Control window on the software console.
   2. Acquire multislice ¹H MR images using rapid acquisition with relaxation enhancement (RARE) sequence in the cross view of the sample or the body of the animal with repetition time 2,200 msec, echo time 8.9 msec, RARE factor 8, field of view 4 x 4 cm², slice thickness 1.0 mm, matrix size 266 x 266, in-plane resolution 150 x 150 µm², and number of averages 6. To start the experiment, click the 'traffic light' button in the Scan Control window on the software console.
   3. Acquire ¹⁹F images using a FLASH sequence in the same region of the ¹H MRI with repetition time 220 ms, flip angle = 30°, echo time 3.078 ms, matrix size 32 x 32, in-plane resolution 1.25 x 1.25 mm², slice thickness 4.0 mm, and number of averages 768. To start the experiment, click the 'GOP' (Go- On- Pipeline) button in the Spectrometer Control Tool window on the software console.
6. After MRI, euthanize the mouse with intraperitoneal injection of 15 µl/g body weight ketamine/xylazine solution (150 mg ketamine/18 mg xylazine per kg body weight) followed by cardiac puncture for exsanguination.
7. To recover a mouse from anesthesia, remove the intraperitoneal catheter but do not leave the animal unattended until it regains sufficient consciousness to maintain sternal recumbency.
8. To measure ¹⁹F-labeled bile acid concentrations^11-13 from organ harvest, maintain anesthesia with ketamine plus xylazine as described above.

Wyniki

The use of MFBA for in vivo MRI to 'see' bile acid transport in real time has great potential for both research and clinical use. Moreover, the methods described here for resection of the gallbladder and biochemical analysis of its contents using liquid chromatography and mass spectrometry provide a means of confirming imaging results. However, the validity of these methods requires precise dosing, timing of assays, and localization of the gallbladder for imaging or surgi...

Dyskusje

The synthesis of CA-lys-TFA and CA-sar-TFMA and the in vitro analysis of their transport using stably transfected Madin-Darby canine kidney cells expressing ASBT and human embryonic kidney cells expressing the sodium/taurocholate co-transporting polypeptide (NTCP) are detailed elsewhere^13,14. Here, the focus is on oral administration of MFBA by gavage to live animals, followed by harvest of the gallbladder, liver, and blood for analysis of MFBA content, and, notably, imaging MFBA in the gallbladder by...

Materiały

Name	Company	Catalog Number	Comments
Duall size-21 all glass tissue grinder	Kimble Chase Life Science, Vineland, NJ	885351-0022
Bruker BioSpec 70/30USR Avance III 7T horizontal bore MR Scanner	Bruker Biospin MRI GmbH, Germany		Use companion Paravision Version 5.1 software (see step 3.5)
Bruker 40 mm 19F/1H dual-tuned linerar volume coil	Bruker Biospin MRI GmbH, Germany		Use companion Paravision Version 5.1 software (see step 3.5)
Waters Acquity UPLC System with Quadrupole Detector	Waters Corporation, Milford, MA
Waters Acquity UPLC ethylene bridged hybrid C8 1.7 μm 2.1 x 50 mm column	Waters Corporation, Milford, MA
Gavage Needle	Braintree Scientific, INC.	N-010	20 G-1.5" curved 2.25 mm ball
2 Stainless Steel Hemostats	VWR	10755-018	4 and 5 inch, straight
Ketamine	MWI Veterinary Supply	501090	Ketamin zetamine 100 mg/ml
Xylazine	Akorn, Inc.		20 mg/ml
Intraperitoneal Catheter	Abbott	AbbocathTM-T.I.V. G720-A01 4535-42	24-G x 0.75"