By K. D. Rainsford (auth.), Timothy S. Gaginella, Gyula Mózsik, K. D. Rainsford (eds.)
The Gastrointestinal component to the foreign Union of Pharmacology (IUPHAR) was once validated in 1994 in Montreal, Canada. The institution of the GI part acknowledges the foreign growth of gastrointestinal pharmacology, together with uncomplicated and human reviews.
The Gastrointestinal component to IUPHAR equipped the 1st symposium, Biochemical Pharmacology as an method of Gastrointestinal illnesses: from easy technology to medical Perspectives, on 10-12 October, 1995, in Pécs, Hungary.
the most issues were:
- Gastrointestinal secretory and excretory fuctions
- Gastrointestinal motility
- Biochemical-pharmacological mechanisms in neural and hormonal activities taken with GI capabilities
- major general and pathological biochemical mechanisms in GI capabilities
- GI mucosal damage and safeguard
- Molecular mechanisms of premalignant and malignant illnesses in GI tract
- Use of remoted cells and mobile cultures in bioochemical-pharmacological reviews to process GI illnesses.
The provided papers are released during this e-book.
Read or Download Biochemical Pharmacology as an Approach to Gastrointestinal Disorders: Basic Science to Clinical Perspectives (1996) PDF
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The Gastrointestinal element of the overseas Union of Pharmacology (IUPHAR) was once demonstrated in 1994 in Montreal, Canada. The institution of the GI part acknowledges the foreign development of gastrointestinal pharmacology, together with uncomplicated and human stories. The Gastrointestinal component of IUPHAR prepared the 1st symposium, Biochemical Pharmacology as an method of Gastrointestinal ailments: from simple technological know-how to scientific views, on 10-12 October, 1995, in Pécs, Hungary.
Extra resources for Biochemical Pharmacology as an Approach to Gastrointestinal Disorders: Basic Science to Clinical Perspectives (1996)
Takeuchi K, Ishihara Y, Okada M, Niida H, Okabe S. A continuous monitoring of mucosal integrity and secretory activity in rat stomach: a preparation using a lucite chamber. Jpn J Pharmacol. 1989;49:235-44. 14. Takeuchi K, Ohtsuki H, Nakagawa S, Okabe S. Characterization of FPL-52694 [5-(2-hydroxypropoxyl)-8-propyl-4-oxo-4H-benzopyran-2-carboxylic acid Na] on histamine release from rat peritoneal mast cells induced by antigen, compound 48/80 and A23187. Agents Actions. 1985;17:10-l3. 15. Takeuchi K, Ohuchi T, Narita M, Okabe S.
Sandvik AK, Waldum HL. CCK-B (gastrin) receptor regulates gastric histamine release and acid secretion. Am J Physiol. 1991;260:G925-8. 18. Nylander A-G, Chen D, Lilja I et al. Enterochromaffin-like cells in rat stomach respond to short-term infusion of high doses of cholecystokinin but not to long-term, sustained, moderate hyper CCKemia caused by continuous cholecystokinin infusion or pancreaticobiliary diversion. Scand J Gastroenterol. 1993;28:73-9. 19. Asahara M, Kinoshita Y, Nakata H et al. Gastrin receptor genes are expressed in gastrin parietal and enterochromaffin-like cells of Mastamys natalensis.
19. Whittle BJR, Lopes-Bermonte J, Moncada S. Regulation of gastric mucosal integrity by endogenous nitric oxide: Interactions with prostaglandins and sensory neuropeptides in the rat. Br J Pharmacol. 1990;99:607-11. 20. Moncada S, Palmer RMJ, Higgs EA. Nitric oxide: Physiology, pathophysiology and pharmacology. Pharmacol Rev. 1991;43:109-42. 21. Takeuchi K, Ohuchi T, Okabe S. Nitric oxide mediates inhibition of gastric acid secretion in the damaged stomach: Interaction with endogenous prostaglandins.