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Irritable Bowel Syndrome Chinwon Rim Department of Chemistry Southern Methodist University.

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Presentation on theme: "Irritable Bowel Syndrome Chinwon Rim Department of Chemistry Southern Methodist University."— Presentation transcript:

1 Irritable Bowel Syndrome Chinwon Rim Department of Chemistry Southern Methodist University

2 What is Irritable Bowel Syndrome(IBS)? A group of functional bowel disorders Chronic abdominal complaints without a structural or biochemical cause Constitutes a major health problem with gastrointestinal (GI) symptoms The cause of IBS is unknown. Affects up to ~20 % adults in the industrialized world The condition is more frequent in women. The direct medical costs of IBS are ~ $ US 8 billion in the US each year.

3 Symptoms of IBS Abdominal discomfort and pain Bloating, mucous in stools, diarrhea, constipation, or alternating diarrhea and constipation Depression, anxiety or stress IBS can be subdivided into  Diarrhea-predominant (IBS-D)  Constipation-predominant (IBS-C)  Alternating diarrhea and constipation

4 Subclassification of patients Supportive symptoms of IBS 1. Fewer than 3 bowel movements a week 2. More than 3 bowel movements a day 3. Hard or lumpy stools 4. Loose or watery stools 5. Urgency 6. Feeling of incomplete bowel movement 7. Passing mucus during a bowel movement 8. Abdominal fullness, bloating or swelling Diarrhea-predominant IBS (IBS-D)  One or more of 2, 4 or 6 and none of 1, 3 or 5 Constipation-predominant IBS (IBS-C)  One or more of 1, 3 or 5 and none of 2, 4 or 6

5 Serotonin is important in gut function GI disorders may be related to  an imbalance of serotonin in the gut  an improper reaction of the digestive system to serotonin  a faulty communication network between serotonin in the gut and the brain and spinal cord. Serotonin plays a major role in modulating intestinal movement and perception of pain. Helps to soften stools by releasing water.

6 Serotonin (5-hydroxytryptamine, 5HT) A monoamine neurotransmitter Found in cardiovascular tissue, the peripheral nervous system, blood cells, and the CNS 95 % resides in the GI tract Serotonergic neurons secrete 5HT The function of serotonin is exerted upon its interaction with specific receptors. 7 distinct families of 5HTreceptors; 5HT 1, 5HT 2, 5HT 3, 5HT 4, 5HT 5, 5HT 6, and 5HT 7

7 5HT 3 receptors and its antagonists 5HT 3 receptors  A ligand-gated cation channel  Present in the GI tract  Control sensation, contraction of intestinal muscle  Release of fluid into the intestines 5HT 3 antagonists  Slow intestinal transit  Decrease intestinal secretions  Decrease the water content of stool  Diminish colonic pain

8 5HT 4 receptors and its agonists 5HT 4 receptors  G-protein-coupled receptor  Present in the GI tract  Mediate both relaxation and contraction of circular smooth-muscle strips  Induces small bowel and to a lesser extent colonic fluid secretion 5HT 4 agonists  Accelerate gastric emptying  Accelerate small and large bowel transit  Increase stool water content

9 Alosetron in IBS-D The first drug is approved for female patients by FDA Brand name is Lotronex ® by Glaxo Smith Kline A potent and selective antagonist of the 5HT 3 receptors

10 Synthetic pathway of alosetron (i) NaH, dimethoxyethane; (ii) HCl.

11 How does alosetron works? The exact mechanism how alosetron relieves the symptoms of IBS-D is unknown. Serotonin in the intestines controls how pain is felt, contraction of intestinal muscle, and release of fluid into the intestines. An excessive release of or an excessive response to serotonin causes a pain and diarrhea. By blocking 5HT 3 receptors, alosetron reduced pain and motor responses.

12 Alosetron-New Drug for IBS-D Alosetron is rapidly absorbed and extensively metabolized. Effective in relieving pain, normalizing bowel frequency, and reducing urgency Constipation is the most common adverse effect Appears to provide a modest benefit to women Should be prescribed under the guidance of a specialist Serious side effects and high-cost maintenance problem

13 T egaserod in IBS-C The first selective serotonin 5HT 4 receptor partial agonist approved by FDA for the treatment of abdominal pain and constipation predominent IBS patients Brand name is Zelnorm TM by Novartis Pharmceu. Corp.

14 Synthetic pathway of tegaserod (i) K 2 CO 3, RBr or ClCOX; (ii) t-BuOCH(NMe 2 ) 2 then H 2, Pd/C; (iii) DMF, POCl 3 ; and (v) N-pentyl-N’-aminoguanidine, MeOH/HCl.

15 How does tegaserod work? The exact mechanism of tegaserod’s action is not yet understood completely. Tegaserod binds with high affinity at 5HT 4 receptors. The activation of 5HT 4 receptors in GI tract stimulates the peristaltic reflex and intestinal secretion. As a result, contractions increase and the increased contractions speed the transit of digesting food and reverse constipation. Reduces the sensitivity of the intestinal pain-sensing nerves and reduces pain by inhibiting visceral sensitivity

16 Tegaserod –a Promising Option Tegaserod is rapidly absorbed and metabolized. Effective in increasing the frequency of stools, relieving abdominal pain and discomfort, and decreasing the sensations of bloating Diarrhea is an occasional side effect. Is approved only for women Should be prescribed under the guidance of a specialist

17 Conclusions Alosetron, 5HT 3 antagonists, appears to provide a modest benefit to women with IBS-D. Offers a new option for the treatment of IBS-D. Tegaserod, 5HT 4 agonists, appears to be a promising options in women with IBS-C not responding to increased dietary fiber or laxative therapy. Both cases, need more researches on mechanism how drugs work and clinical studies for the treatment of men patients. Need to discover new drugs for alternating diarrhea and constipation

18 References 1. De Ponti, F.; Tonini, M. Drugs 2001, 61(3), 317-32. 2. Lembo, A.; Weber, H. C.; Farraye, F. A. Drugs 2003, 63(18), 1895- 905. 3. Talley, N. J. Lancet 2001, 358(9298), 2061-8. 4. 5. Coates, I. H. O., Alexander William; North, Peter Charles; Tyers, Michael Brian. Eur. Pat. Appl. (1990), 9 pp. 6. Buchheit, K.-H.; Gamse, R.; Giger, R.; Hoyer, D.; Klein, F.; Kloppner, E.; Pfannkuche, H.-J.; Mattes, H. Journal of medicinal chemistry 1995, 38(13), 8. 7. Camilleri, M. Aliment Pharmacol Ther 2001, 15(3), 277-89. 8. Appel-Dingemanse, S. Clin Pharmacokinet 2002, 41(13), 1021-42.

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