Endocannabinoid and Cannabinoid-Like Fatty Acid Amide Levels Correlate with Pain-Related Symptoms in Patients with IBS-D and IBS-C: A Pilot Study
Endocannabinoids in IBS
Snyder Institute for Chronic Diseases, University of Calgary, Calgary, Alberta, Canada
Department of Medicine, Division of Gastroenterology, University of Calgary, Calgary, Alberta, Canada
Department of Biomolecular Chemistry, Faculty of Medicine, Medical University of Lodz, Lodz, Poland
Department of Digestive Tract Diseases, Faculty of Medicine, Medical University of Lodz, Lodz, Poland
Center for Drug Discovery, Northeastern University, Boston, Massachusetts, United States of America
Faculty of Applied Mathematics, AGH University of Science and Technology, Cracow, Poland
Department of Cytobiochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland
Faculty of Mathematics and Computer Science, Jagiellonian University, Cracow, Poland
Department of Medicine, Division of Gastroenterology, Ludwig Maximilians University of Munich, Munich, Germany
Medical University of Gdańsk, Poland
* E-mail: Martin.Storr@med.uni-muenchen.deAbstract
Aims
Irritable bowel syndrome (IBS) is a functional gastrointestinal (GI) disorder, associated with alterations of bowel function, abdominal pain and other symptoms related to the GI tract. Recently the endogenous cannabinoid system (ECS) was shown to be involved in the physiological and pathophysiological control of the GI function. The aim of this pilot study was to investigate whether IBS defining symptoms correlate with changes in endocannabinoids or cannabinoid like fatty acid levels in IBS patients.
Methods
AEA, 2-AG, OEA and PEA plasma levels were determined in diarrhoea-predominant (IBS-D) and constipation-predominant (IBS-C) patients and were compared to healthy subjects, following the establishment of correlations between biolipid contents and disease symptoms. FAAH mRNA levels were evaluated in colonic biopsies from IBS-D and IBS-C patients and matched controls.
Results
Patients with IBS-D had higher levels of 2AG and lower levels of OEA and PEA. In contrast, patients with IBS-C had higher levels of OEA. Multivariate analysis found that lower PEA levels are associated with cramping abdominal pain. FAAH mRNA levels were lower in patients with IBS-C.
Conclusion
IBS subtypes and their symptoms show distinct alterations of endocannabinoid and endocannabinoid-like fatty acid levels. These changes may partially result from reduced FAAH expression. The here reported changes support the notion that the ECS is involved in the pathophysiology of IBS and the development of IBS symptoms.
Introduction
Irritable bowel syndrome (IBS) is a functional gastrointestinal (GI) disorder, associated with alterations of bowel function and other symptoms related to the GI tract, such as abdominal pain or cramping (localized, intermittent pain), bloating or feeling of incomplete evacuation. The prevalence of IBS is estimated at up to 20% in the Western countries [1,2] and accounts for more than 50% of referrals to GI specialists [3–5]. IBS has a major impact on patient’s quality of life, and accounts for a heavy burden for, patients, health care providers and economies. Due to the lack of efficient treatments, there is an unmet need to develop novel anti-IBS strategies.
The design of novel therapeutics to be used in IBS is impaired by our incomplete understanding of the pathophysiology of IBS and therefore the poor control of the changes in endogenous systems during IBS development. Therefore the systems that are well-known for their involvement in pain signalling and GI motility are currently regarded as being a main potential target for future anti-IBS drugs. The endogenous cannabinoid system (ECS), which consists of three principal pillars, i.e. “classical” cannabinoid (CB1, CB2) and “non-classical” (TRPV1, GPR55) receptors, endogenous ligands (anandamide, AEA; 2-arachidonyloglycerol, 2-AG) and the cluster of enzymes, responsible for CB synthesis and degradation [6] has recently attracted much attention as a crucial site in IBS pathophysiology. The localization of CB1 and CB2 receptors and their endogenous ligands in the GI tract and in sensory endings on primary sensory afferents [7–11], as well as participation of the ECS in pain signalling, modulation of sensory afferent information and GI peristalsis (for review, see: [6,12]) have been well established. However, much attention has currently been given to the fatty acid amide hydrolase (FAAH) and its metabolites. FAAH is an intracellular enzyme, primarily located in the liver and the brain, as well as in peripheral organs, like the GI tract (for review, see: [13]). It is commonly accepted that AEA is the main substrate for FAAH, but a growing body of evidence points that 2-AG, although not exclusively, is also deactivated by this hydrolase [14]. FAAH is also involved in the degradation of several other biolipids, including palmitoylethanolamide (PEA) and oleoylethanolamide (OEA), which may bind to both, “classical” and “non-classical” CB receptors. Therefore it has been suggested that the modulators of the FAAH activity, as potential anti-IBS therapeutics, may provide finer tuning of the ECS function than the CB receptor ligands, also in terms of peripheral vs. central site-dependent site effects.
To further clarify whether the ECS is involved in IBS pathophysiology and whether changes in ECB or cannabinoid-like fatty acid amide levels contribute to clinical symptoms we established ECB and cannabinoid-like fatty acid amide levels in female patients with IBS. The levels where then correlated with IBS subtypes, namely IBS-D and IBS-C and, additionally, with the self-reported symptom scores and compared to age-matched female control group. Finally, FAAH mRNA levels were evaluated in colonic biopsies from female IBS-D and IBS-C patients and matched controls to investigate whether changes in FAAH expression at the transcription level contribute to the observed changes in metabolite concentrations. The correlations observed may provide a new understanding of the mechanisms underlying IBS and disturbances associated with GI functional and abdominal pain processing.
Materials and Methods
Ethics Statement
Human studies were approved by the Ethics Committee of the University of Calgary, Canada and Medical University of Lodz, Poland. All participating subjects gave written, informed consent prior to genetic analysis.
Patients
Endocannabinoid and cannabinoid-like fatty acid amide levels were quantified in plasma from female IBS-D and IBS-C patients and healthy controls at the GI-clinic of the University of Calgary, Canada. In total 21 blood samples were analyzed. The study population comprised 7 patients with IBS-D (age 26-58), 7 patients with IBS-C (age 21-62), and 7 healthy subjects (age 29-56).
To quantify the relative expression of human FAAH, forceps biopsy samples were analyzed. In total 16 samples prepared from human colon biopsies were used for the study. The study population comprised 3 patients with IBS-D (age 43-71), 3 patients with IBS-C (age 25-62) and 10 healthy, unrelated controls (age 33-82) recruited from January 2011 to December 2012 at the Medical University of Lodz, Poland.
The diagnosis of IBS-D and IBS-C was assessed according to established clinical criteria using endoscopic, radiologic, and histopathologic examinations.
Endocannabinoid and and cannabinoid-like fatty acid amide extraction from plasma
After collection, human plasma samples from each patient were kept at room temperature for 1,30, 60 and 120 minutes and were then immediately stored at -80°C until they were processed and analyzed. The extraction procedure for the standards, made in 20 mg/mL fatty acid free BSA, quality control samples, made in BSA, unextracted quality control samples, made in ethanol, and plasma samples was a modified version of the Folch extraction [15–17]. Proteins were precipitated in the standards, quality controls made in BSA and plasma samples using ice cold acetone:PBS, pH 7.4 (3:1) and internal standard, followed by centrifugation at 13,000 g for 5 minutes at 4°C. The resulting supernatant from all samples was dried under nitrogen until the acetone was removed. To the remaining supernatant, 100 µL PBS, one volume of methanol and two volumes of chloroform was added for liquid-liquid phase extraction of the lipids. The two phases were separated by centrifugation and the bottom organic layer was evaporated to dryness under nitrogen. Samples were reconstituted in 50 µL ethanol and were vortexed, sonicated briefly and centrifuged prior to analysis.
Nano LC-MS analysis for endocannabinoids
Samples were loaded on a C4 LC trap (5 µm, 300 A, Bruker-Michrom, Auburn, CA, USA) with water/acetonitrile/formic acid (80/20/0.1) at a flow rate of 10 µL/min for 3 min. Chromatographic separation was achieved using a Michro-Tech Scientific C18 column (50 mm, 75 µm ID, 3 µm particle, 120 A pore size) on an ABI 4000 Q-Trap mass spectrometer with a Tempo nano-LC on the front end (Applied Biosystems Inc., Framingham, MA). The mobile phase consisted of water/acetonitrile (95/5; A) and acetonitrile/water (95/5; B), with 0.1% formic acid in both, in the following two step gradient: initial conditions of 80% A decreased linearly to 20% A over 1 minute and to 100% B in 9 min. The system was held at these conditions for 5 minutes before returning to initial conditions (flow rate = 700 nl/min); the autosampler was kept at 4°C to prevent analyte degradation. The sample injection volume was 1µL and the reagent used to fill the loop (10 µL) was water/acetonitrile (95/5) with 0.1% formic acid. Eluted peaks were ionized using a nanoESI source on a 4000Qtrap (Applied Biosystems) in positive mode and detected by multiple reaction monitoring (MRM). Deuterated internal standards were used for each standard curve and the levels of each endocannabinoid or cannabinoid-like fatty acid amide per mL plasma were determined.
Standard curves were linear with a regression value of >0.993. Extraction efficiencies were greater than 85% for each compound and deuterated standard.
Real-time reverse transcriptase (RT) PCR and quantification of FAAH expression in human biopsies
The biopsy specimens were immediately frozen after isolation and kept at -70°C until processing. The RNA was isolated using the PureLink RNA Mini kit (Life Technologies, Carlsbad, CA, USA) according to manufacturer’s protocol. The purity and quantity of isolated RNA was measured using dedicated spectrophotometer (BioPhotometer; Eppendorf, Germany). Total RNA (1 μg) was used for cDNA synthesis using a first strand cDNA synthesis kit (Fermentas, Canada). Quantitative analysis was performed using fluorescently labeled TaqMan probes Hs00155015_m1 and Hs01003267_m1 for human FAAH and hypoxanthine-guanine phosphoribosyltransferase (HPRT, endogenous control), respectively (Life Technologies, Carlsbad, CA, USA) on Mastercycler S realplex 4 apparatus (Eppendorf, Germany). All experiments were performed in triplicates.
The Ct values for studied genes were normalized to Ct values obtained for a housekeeping gene HPRT. Relative amount of mRNA copies was calculated using 2^-ΔCt method. For presentation, relative copy number values were recalculated to number of copies of each studied gene per 1000 copies of HPRT. The mean Ct values for the housekeeping gene (HPRT) in samples from all patient groups did not alter regardless of the studied group.
Statistical analysis
Statistical analysis was performed in R software environment for statistical computing.
Level of significance was set in all tests to P ≤ 0.05. Statistical significance in the differences in levels (measured after 0, 30, 60 and 120 min) of AEA, 2-AG, OEA and PEA for different symptoms was tested using multivariate analysis of variance (MANOVA; 4 different tests were used: Pillai, Wilks, Hotelling-Lawley and Roy test). Each symptom was treated separately and compared with control group. In the case of symptoms, which showed difference in levels, an analysis of variance was applied (one-way ANOVA) to each measurement time (0, 30, 60, and 120 min). The LSD test was used in post hoc analysis (with Holm's p value adjustment). To establish correlations between disease type and specific symptoms, the χ2 test with Bonferroni correction was used.
ANOVA followed by Bonferroni post-hoc testing was used to assess the differences among relative FAAH mRNA levels. P values < 0.05 were considered statistically significant.
Figures were prepared using Prism 5.0 (GraphPad Software Inc., La Jolla, CA, USA).
Results
Endocannabinoid and cannabinoid-like fatty acid amide plasma levels change with stool pattern in IBS
Endocannabinoid (AEA, 2-AG) and cannabinoid-like fatty acid amide (OEA, PEA) levels were detected in all plasma samples from IBS-D and IBS-C patients and healthy controls. In all patients AEA, OEA and PEA levels increased, while 2-AG level did not change over the time of the study, suggesting the release from peripheral blood cells, an observation which is congruent with earlier reported results [17]. In IBS-D patients, 2-AG levels were higher, whereas OEA and PEA levels were lower than in healthy controls (Figure 1). In contrast, OEA plasma levels were higher in IBS-C patients vs. healthy subjects.
MANOVA analysis showed no significant correlation between endocannabinoid and cannabinoid-like fatty acid amide plasma levels and IBS type.
PEA plasma levels are correlated with abdominal cramping frequency in IBS patients
As shown in Figure 2, PEA levels were considerably lower in IBS-D and IBS-C patients with daily cramping, but equal or increased in patients suffering from >1/week or less frequent cramping, compared to healthy subjects. Low levels of PEA were detected in IBS-C patients with no symptoms of cramping (Figure 2).
Decreased FAAH expression in IBS-C patients vs. healthy controls
There was no difference in the FAAH expression at mRNA level between female IBS-D patients and healthy controls (Figure 3). However, a significant decrease in FAAH mRNA levels was detected in colonic biopsies from female IBS-C patients compared to healthy controls.
Discussion
In this preliminary study on a small cohort of IBS patients we have shown that the biolipid turnover may play a crucial role in the pathophysiology of IBS and the levels of FAAH metabolites correlate with the motility pattern and disease symptoms. We have also observed that FAAH mRNA levels are correlated with the IBS type and a significant decrease in FAAH mRNA expression was confirmed in patients suffering from IBS-C. Finally, we have demonstrated that the biolipid turnover in IBS, although greatly dependent on FAAH activity, is also regulated by other enzymatic pathways, which need further elucidation.
Cannabinoids have been used for centuries for recreational purposes, but only relatively recently their potential clinical action attracted much attention. Although the localization and function of the components of ECS are not fully understood and are still under investigation in several systems [18,19], it has become evident that they play a crucial role in functional GI disorders, such as IBS, and targeting the ECS may become one of major sites of action of anti-IBS treatments. Targeting CB receptors, which are localized on the neural, immune and other non-neural cells, by endogenous and exogenous cannabinoids may alter central or enteric GI muscle excitation [20] and visceral hypersensitivity (for review, see: [6]). However, in extensive clinical studies CB receptor ligands, like dronabinol and Δ9-tetrahydrocannabinol, failed to produce a simultaneous relief of both major symptoms of IBS, pain and changes in motility patterns [21]; they were also shown to act in the central nervous system and thus produced side effects at higher doses, which may have masked the potential beneficial action [22]. In contrast, FAAH and MAGL blockers produce potent antinociceptive effects and regulate GI motility. However, behavioral side effects typical for CB agonists are absent only in animals treated with selective FAAH [23,24], but not selective MAGL or mixed FAAH/MAGL inhibitors [25–27]. Moreover, sustained FAAH blockade does not alter CB1 receptor function and lacks dependence liability [28,29], suggesting that blocking the enzyme is a promising anti-IBS strategy. FAAH as a potential target in IBS treatment has also been proposed by the group of M. Camilleri, who investigated genetic variation in endocannabinoid metabolism in IBS patients [21,30,31].
Our study suggests that the motility patterns in IBS patients may correlate with biolipid serum levels. The endocannabinoid and cannabinoid-like fatty acid amide homeostasis is finely tuned in human body by synthesis on demand and rapid intracellular degradation, in which both degrading enzymes and transmembrane transporters are involved. Our observations require thus further extension, since prolonged changes in the biolipid equilibrium may have both, diagnostic and therapeutic implications. Furthermore, our data suggests that not only typical endocannabinoids, but also biolipids binding to “non-classical” CB receptors may be involved in the IBS pathophysiology, what could be important for the understanding of the disease. Earlier studies focused mainly on AEA and 2-AG in the colon and small intestine and showed that AEA may be the major endocannabinoid influencing GI function [32,33]. However, it was later reported that cannabinoid-like fatty acid amides, such as PEA and OEA, can also be found in the GI tract and are able to reduce intestinal motility [34–36]. Although there is conflicting data on the involvement of the “non-classical” CB receptors in the anti-motility effect and the modulation of basal visceral sensitivity by PEA and OEA, which still needs to be elucidated [37–39], it is apparent that several components of the ECS play important roles in the development of IBS.
Finally, we have shown that the FAAH mRNA expression is decreased in patients with IBS-C. This suggests slower turnover of endocannabinoids and may in part elegantly explain the slowing of motility, a typical feature of IBS-C. However, lower FAAH mRNA levels are in contrast with decreased PEA concentrations found in the IBS-C patient plasma, since this fatty acid amide is one of the substrates for FAAH and should be accumulated in the absence of enzyme activity. This suggests that other degradation enzymes are involved in PEA metabolism in the course of IBS. On the other hand, since samples for quantification of FAAH mRNA expression and endocannabinoid levels originated from two separate groups of patients, this hypothesis needs further elucidation.
In conclusion, our study shows that two major pillars of the ECS, the enzyme FAAH and its metabolites, correlate with IBS subtypes and IBS symptoms, whereas the basal release of the biolipids is not altered. Here we report that the alterations in endocannabinoids or cannabinoid-like fatty acid amides are associated with symptoms arising from altered motility and nociception and suggest their pathophysiological involvement. For IBS-C, the increased OEA levels may be due to the reduced FAAH expression and in consequence contribute to delayed intestinal transit in these patients. In contrast, the reduced OEA levels in patients with IBS-D may contribute to the increased GI transit. Our study furthermore provides evidence that the biolipid PEA level is lower in patients who report daily cramping and we suggest that the lack of PEA, which was shown to induce antinociception in animals, is an important component underlying the increased abdominal pain in patients with both IBS subtypes. Finally, our study for the first time shows that altered FAAH expression and distinct alterations in ECB or cannabinoid-like fatty acid amide levels are associated with motility phenomena like diarrhea and constipation, as well as symptoms of increased nociception and constitute that the endocannabinoid system is a crucial player in the pathophysiology of IBS. However, since samples for quantification of FAAH mRNA expression and endocannabinoid levels originated from two separate groups of patients, this hypothesis needs further elucidation.