allopurinol and Irritable-Bowel-Syndrome

allopurinol has been researched along with Irritable-Bowel-Syndrome* in 2 studies

Other Studies

2 other study(ies) available for allopurinol and Irritable-Bowel-Syndrome

ArticleYear
Antioxidant Supplements and Gastrointestinal Diseases: A Critical Appraisal.
    Medical principles and practice : international journal of the Kuwait University, Health Science Centre, 2017, Volume: 26, Issue:3

    The gastrointestinal tract digests and absorbs dietary nutrients, protects the body against physical and chemical damage from contents in its lumen, provides immunity against external antigens, and keeps an optimum environment for the gut microbiota. These functions cannot be performed normally in several diseases of which the following are discussed here: irritable bowel syndrome and inflammatory bowel disease, which includes Crohn's disease and ulcerative colitis. Because these diseases are associated with oxidative stress, a host of antioxidant supplements are used for maintenance and recovery of the gut functions. However, the benefits of these supplements have not been established. The available 80 human trials were rated for levels of confidence and for benefits of the antioxidant supplements. For Crohn's disease, the supplements for which clear benefits occurred in at least 2 studies were allopurinol, Boswellia serrata (frankincense or shallaki), Artemesia species (wormwood), Tripterygium wilfordii (léi gōng téng), and omega-3 fatty acids. Similar beneficial supplements for ulcerative colitis were allopurinol, Matricaria chamomilla (chamomile), Curcuma longa (curcumin in turmeric), and omega-3 fatty acids. There was also a clear benefit for ulcerative colitis in 2 studies where a multiherbal Chinese medicine preparation and an Ayurvedic medicine preparation were used. For irritable bowel syndrome, there was only a marginal benefit of some of the antioxidant supplements. Thus, some antioxidant supplements may be beneficial at certain stages of specific diseases. This is consistent with the current concept that antioxidants act by inhibiting oxidative stress pathways in a tissue- and environment-specific manner and not by simply acting as scavengers.

    Topics: Allopurinol; Antioxidants; Colitis, Ulcerative; Crohn Disease; Dietary Supplements; Fatty Acids, Omega-3; Gastrointestinal Microbiome; Gastrointestinal Tract; Humans; Inflammatory Bowel Diseases; Irritable Bowel Syndrome; Medicine, Traditional; Plants, Medicinal

2017
The role of oxidants and reactive nitrogen species in irritable bowel syndrome: a potential etiological explanation.
    Medical science monitor : international medical journal of experimental and clinical research, 2013, Sep-13, Volume: 19

    The aim of this study was to evaluate the plasma concentrations of malondialdehyde (MDA) and nitric oxide (NO) and the plasma activities of oxidant and antioxidant enzymes in patients with IBS.. A total of 36 patients with IBS were included in the study. Thirty-five healthy subjects were selected to form the control group. Superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px), xanthine oxidase (XO), adenosine deaminase (AD) activities, and malondialdehyde (MDA) and nitric oxide (NO) concentrations were studied in the serum samples of all patients and controls.. Plasma XO and AD activities, and MDA and NO concentrations were significantly higher in IBS patients than in controls. The SOD, CAT, and GSH-Px activities in the serum of patients with IBS were significantly lower than that of controls.. These results suggest that lipid peroxidation and alterations in the oxidant-antioxidant enzymatic system may play a role in the pathogenesis of IBS. Increased lipid peroxidation in IBS may be related to an increase in NO level and XO activity and a decrease in antioxidant enzymes activities. In addition, increased AD activity may have a role in immunological changes of IBS patients.

    Topics: Adenosine Deaminase; Adult; Catalase; Female; Glutathione Peroxidase; Humans; Irritable Bowel Syndrome; Lipid Peroxidation; Male; Malondialdehyde; Middle Aged; Nitric Oxide; Oxidoreductases; Superoxide Dismutase; Xanthine Oxidase

2013