- Research article
- Open Access
Inhibition of pancreatic cholesterol esterase reduces cholesterol absorption in the hamster
© Heidrich et al; licensee BioMed Central Ltd. 2004
- Received: 30 October 2003
- Accepted: 19 April 2004
- Published: 19 April 2004
Pancreatic cholesterol esterase has three proposed functions in the intestine: 1) to control the bioavailability of cholesterol from dietary cholesterol esters; 2) to contribute to incorporation of cholesterol into mixed micelles; and 3) to aid in transport of free cholesterol to the enterocyte. Inhibitors of cholesterol esterase are anticipated to limit the absorption of dietary cholesterol.
The selective and potent cholesterol esterase inhibitor 6-chloro-3-(1-ethyl-2-cyclohexyl)-2-pyrone (figure 1, structure 1) was administered to hamsters fed a high cholesterol diet supplemented with radiolabeled cholesterol ester. Hamsters were gavage fed 3H-labeled cholesteryl oleate along with inhibitor 1, 0–200 micromoles. Twenty-four hours later, hepatic and serum radioactive cholesterol levels were determined. The ED50 of inhibitor 1 for prevention of the uptake of labeled cholesterol derived from hydrolysis of labeled cholesteryl oleate was 100 micromoles. The toxicity of inhibitor 1 was investigated in a 30 day feeding trial. Inhibitor 1, 100 micromoles or 200 micromoles per day, was added to chow supplemented with 1% cholesterol and 0.5% cholic acid. Clinical chemistry urinalysis and tissue histopathology were obtained. No toxicity differences were noted between control and inhibitor supplemented groups.
Inhibitors of cholesterol esterase may be useful therapeutics for limiting cholesterol absorption.
- Cholesterol Absorption
- Cholesterol Ester
- Cholic Acid
Primary hypercholesterolemia is an established risk factor of atherosclerosis and coronary heart disease (CHD) . Epidemiological data indicate a positive relationship between serum LDL-cholesterol and CHD, which is the leading cause of death in both men and women in the United States. Clinical trials have shown that cholesterol-lowering regimens are beneficial for prevention of CHD morbidity and mortality. A variety of regimens are being used to lower serum cholesterol including diet restriction, nicotinic acid, bile acid sequestering agents, and HMGCoA reductase inhibitors. Reductase inhibitors have become widely used . Although generally well tolerated and effective, side effects have been reported in significant numbers of participants in controlled trials, including increases in serum levels of hepatic transaminases, increases in creatine kinase, muscle weakness, GI disturbances, headache, and sleep disorders. With prolonged use, other side effects have been noted including depression , sensorimotor neuropathy , and eczema . Alternative therapies are needed, especially for populations that cannot tolerate reductase inhibitors
Dietary cholesterol is comprised of free and esterified cholesterol, the ratio depending upon dietary source. In diets rich in meats, a significant percentage of cholesterol is esterified. Hydrolysis of cholesterol ester in the lumen of the small intestine is catalyzed by cholesterol esterase (CEase), EC184.108.40.206, which liberates free cholesterol. Free cholesterol mixes with cholesterol contained in bile secretions to form the pool of absorbable cholesterol. Due to the low solubility of cholesterol, solubilization of cholesterol by bile salts and lecithin into micelles is essential. In addition, transport proteins are required to deliver cholesterol from micelles to the enterocytes for absorption. CEase provides the hydrolytic activity for hydrolysis of cholesterol ester and may provide the transport function for delivery of cholesterol from micelles to enterocytes , although this has not been clearly established . Inhibitors of CEase may provide a method to limit the bioavailability of dietary cholesterol derived from cholesterol esters and may also limit the absorption of free cholesterol.
To circumvent the lack of selectivity of 2, we developed 6-chloro-3-(1-ethyl-2-cyclohexyl)-2-pyrone, 1 (figure 1) as a selective and reversible inhibitor of CEase . This involved replacing the aromatic 3-benzyl group in 2 with an aliphatic ring tethered to the 3-position. Inhibition of CEase is very sensitive to the length of the tether. Compound 1 is a potent inhibitor of CEase (Kd = 25 nanomolar) and is highly selective for CEase compared to other serine hydrolases such as chymotrypsin . Therefore, compound 1 can now be considered the prototype for development of selective inhibitors of CEase. In the present study, we carried out an animal model study of the effects of 1 on the absorption of cholesterol derived from cholesteryl oleate to test whether 1 is active in vivo.
To investigate the toxic effects of 1, the inhibitor was administered to animals for 30 days. Animals treated with inhibitor 1 at 100 and 200 micromoles per day were compared to controls through clinical chemistries, necropsy and histopathology. There were no differences between treated and control animals based upon clinical chemistries (liver enzymes and proteins, renal function indices, and electrolytes). No lesions were noted on necropsy. In addition, there were no noted differences between treated and control animals in the histopathology exam (heart, lung, liver, pancreas, GI tract, thyroid, lymph nodes).
There may be additional physiological roles of pancreatic cholesterol esterase
CEase is also synthesized in lactating mammary glands and is secreted into milk in a number of species including human. Pancreatic and milk CEase are derived from the same gene . It appears that the same enzyme is present in serum  and is synthesized by human macrophages , eosinophils , endothelial cells , and liver . The physiological roles of CEase that is present in these various locations are not clear, nor is it known whether inhibitors designed to block hydrolysis of dietary cholesterol esters through inhibition or inactivation of CEase in the intestine will have additional biological effects. It is noteworthy that the lipid-lowering effect of WAY-121,898, a novel carbamate inhibitor of CEase, was observed both by oral and by parenteral administration of the drug . This apparent broad distribution of CEase expression, however, has been questioned in a recent report of tissue levels of CEase mRNA in which only pancreatic and intestinal tissues were positive .
Cholesterol esterase has a major physiological role in cholesterol ester hydrolysis
The major physiological role of CEase in determining the bioavailability of dietary cholesterol esters is supported by in vivo studies of CEase inhibitors [8, 17, 19] and by studies with CEase gene knockout mice where impaired absorption of cholesterol ester was observed . Gene knockout mice, however, did not exhibit impaired absorption of unesterified cholesterol which suggests that CEase does not have a direct cholesterol transport function. This conclusion differs from the results of a number of studies with rats in which unesterified cholesterol absorption was decreased in animals made CEase deficient by removing pancreatic juice  or by treating pancreatic juice with antibody to CEase . CEase increased the absorption of free cholesterol into cultured Caco-2 cells  and into gut sacs , further suggesting a transport role for CEase. Other studies, however, did not support a role for CEase in transport of unesterified cholesterol to enterocytes; uptake of cholesterol by Caco-2 cells has been reported to be independent of added CEase or of transfection with CEase cDNA [24, 25]. These conflicting reports regarding a transport function for CEase may reflect structural differences in the various CEase used in these studies. The C-termini of CEase possess a consensus proline-rich eleven-amino acid repeat sequence (PVPPTGDSGAP)n, which differs among species in the number of repeats, followed by an extreme C-terminus conserved nine-amino acid consensus sequence (AQMPVVIGF). The number of repeats varies from 2–4 in most animals to 16 in human. These proline-rich repeats allow CEase to bind to membrane-associated heparin, and it has been suggested that this may facilitate cholesterol transport . However, a recent clinical trial with CVT-1 (sodium cellulose sulfate), a potent and specific inhibitor of human CEase that binds to the heparin binding site on CEase, did not block absorption of unesterified cholesterol , which suggests that CEase does not have a role in transport of free cholesterol in humans.
Cholesterol esterase appears to have an indirect but essential role in absorption of free cholesterol
A number of different types of inhibitors of cholesterol esterase have been developed
In summary, inhibitor 1 was demonstrated to limit the bioavailability of cholesterol derived from hydrolysis of cholesterol ester. Inhibitor 1 can be considered a prototype of selective inhibitors of CEase that appear to have low toxicity in vivo. It remains to be demonstrated whether inhibition of CEase may also limit the absorption of free cholesterol.
Animals and diets
All animals were housed and treated in compliance with the NIH's Guide for the Care and Use of Laboratory Animals and the Animal Welfare Act. Outbred male Golden Syrian hamsters, 100–125 gm (Charles River Labs.), were housed individually. Animals were acclimated to a light cycle of 12 hours light, 12 hours dark, for one week prior to the beginning of any experiment and randomly assigned to treatment and control groups. Unless indicated, all animals in the study were fed a custom prepared rodent diet, AIN76 (ICN Biologicals, Aurora, Ohio) and water ad libitum. Treatment protocols consisted of feeding a custom rodent diet containing unlabeled free cholesterol and cholic acid to which was added cholesteryl oleate and varying amounts of inhibitor 1. Diets were provided daily in predetermined amounts calculated to maintain normal growth. The basal composition of the semipurified hamster diet contained: casein, 20%; DL-methionine, 0.3%; sucrose, 50%; corn starch, 15%; Alphacel, 5%; corn oil, 5%; choline bitartrate, 0.2%; mineral mix (AIN), 3.5%; vitamin mix (AIN) 1%.
Acute cholesterol absorption measurements
Cholesterol absorption was assessed using a modification of the method reported by Harwood et al. . Male Golden Syrian hamsters were fed the custom diet containing 1% cholesterol and 0.5% cholic acid for three days and then fasted overnight. The following morning hamsters were gavage fed inhibitor 1 at various doses of 0, 20, 40, 80, 120, 160 and 200 micromoles (corresponding to 0 to 48 mg of inhibitor 1), respectively, suspended in a 10% aqueous ethanol solution containing 0.25% methylcellulose and 0.6% Tween-80 as suspending agents. Dosing was 0.5 ml/100 g of body weight. Immediately thereafter, hamsters received an oral bolus, 1.5 ml/hamster, of vegetable oil containing 3H-labeled cholesteryl oleate (1 μCi), and unlabeled cholesteryl oleate (15 mg). The degree of cholesterol absorption was assessed by the serum and hepatic levels of 3H-cholesterol measured over the next 24 hours. Hamsters were anesthetized with isoflourane and blood was obtained by cardiac puncture for determination of serum cholesterol. Animals were euthanized, while anesthetized, by exsanguination. At necropsy, organs including liver, gall bladder, spleen, kidneys, heart, lungs, stomach and intestines, testicles, and the carcass were weighed. Livers were excised and saponified in 5 ml of 2.5 M KOH for 2 hours at 70°C. Aliquots (0.2 mL) of the saponified livers were decolorized with H2O2 (0.2 mL of 30%), neutralized with 3 N HCl (0.2 mL), and then counted in a liquid scintillation counter. Total hepatic radioactivity was calculated from the radioactivity in each aliquot after adjusting for the total volume of the saponified liver. The percent inhibition of cholesterol absorption was determined by comparing the hepatic radioactivity in hamsters receiving inhibitor and hamsters receiving only the vehicle.
Thirty day toxicity study of inhibitor 1
Toxicity data were obtained by monitoring blood chemistry values and urine over a 30 day period, using a modified method reported by DeNinno et al . Male Golden Syrian hamsters were acclimated for 1 week to eating powdered custom diet. Weights of the animals and food consumption were monitored daily. Three groups of hamsters were fed the powdered custom diet containing 1% cholesterol and 0.5% cholic acid. The control group (n = 6) ate only custom diet for 30 days. One group of 6 hamsters was given the optimum dose of inhibitor (100 micromoles) added to the powdered diet daily for 30 days. The third group received the powdered diet with 200 micromoles of inhibitor for 30 days. Blood and urine samples were collected every 5 days by chamber induction of Isoflurane anesthesia, cardiac puncture, and cystocentesis. At 30 days the hamsters were anesthetized by chamber induction and euthanized by exsanguination. At necropsy, organs including liver, gall bladder, spleen, kidneys, heart, lungs, stomach and were weighed. A complete necropsy with histopathology of all organs was carried out. Saponification of liver tissue was carried out as described as above. Tubes were mixed and placed at -20°C for 15 min to enhance precipitation of protein before addition of 4 ml of hexane. After vigorous vortexing, samples were centrifuged at 1500 g for 5 min to separate phases; 3 ml of the hexane phase was evaporated to dryness under N2 before being redissolved in 0.3 mL of 1% (v/v) Triton X-100 in ethanol. Cholesterol levels were analyzed using a commercial assay kit. Triplicate 15 uL aliquots were analyzed in 96-well microtiter plates; 0.2 mL of reagent was added and the plates incubated at room temperature for 1 hr. Absorbance was read at 490 nm using a microtiter spectrophotometer and compared to a standard curve to calculate cholesterol mass.
Supported by SBIR grant DK58440 and NIH grant HL68598
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