File:Determinants of Gastric Acid Secretion.svg
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[编辑]描述Determinants of Gastric Acid Secretion.svg |
English: There are several neuronal, endocrine, and paracrine determinants of gastric acid secretion. Parietal cells in the fundus and body of the stomach are responsible for secretion of acid into the stomach. Major receptors on parietal cells that trigger acid release when activated include the M3 muscarinic, the H2 histaminic, and the CCK-B or gastrin receptor. The respective ligands for these receptors are acetylcholine, histamine, and gastrin. Acetylcholine is released from enteric neurons, histamine is released from enterochromaffin-like cells, and gastrin is released from G cells which are generally found in the antrum, or lower portion, of the stomach. Enterochromaffin-like (ECL) cells are generally found below the epithelial cell layer of the stomach lumen. ECL cells express M3 muscarinic, ST2 somatostatin, and CCK-B gastrin receptors. While M3 and CCK-B receptors trigger histamine release when activated, the ST2 somatostatin receptor inhibits histamine release. Thus, gastrin is pro-acid, and somatostatin is anti-acid secretion. Both somatostatin and gastrin are released primarily from cells in the antrum. G cells secrete gastrin, and D cells secrete somatostatin. D cells have a regulatory role over G cells in that the somatostatin that they release has an inhibitory influence on gastrin secretion from G cells. This serves to reduce futile simultaneous pro-acid and anti-acid signals to the fundus and body of the stomach. A major trigger for gastrin release is the presence of protein in the antrum: this serves to enhance acid secretion, which is necessary for the activity of pepsin, a major digestive enzyme in the stomach which is important for protein breakdown. In addition, D cells are also subject to regulation by gastric luminal contents. In particular, D cells release more somatostatin when the antral pH is low (i.e., when a highly acidic condition exists). This serves as a negative feedback when acid levels are high, as somatostatin will be secreted, enter the gastric bloodstream, and signal to ECL cells to reduce histamine release. Reduced histamine release will, in turn, reduce acid secretion from parietal cells. Finally, our gastric cells would be susceptible to damage from acid and pepsin if they had no protection. Protection of the gastric mucosal cells is in two forms, a physical barrier of viscous mucus, and a chemical defense of bicarbonate, which neutralizes acid. Protective prostaglandins, i.e., PGE2 and PGI2 activate EP3 receptors on non-parietal mucosal cells to enhance mucus and bicarbonate secretion. At the same time, EP3 receptors are activated on parietal cells to inhibit acid secretion. This is primarily a result of EP3's coupling to the G-protein, Gi, which reduces cyclic adenosine monophosphate (cAMP) levels. The proton pump in parietal cells is an exchanger of potassium and protons. Many portions of the physiology of gastric acid secretion are influenced by drugs, especially those used to treat peptic ulcer disease (PUD) and gastroesophageal reflux disease (GERD). The drug classes and sites of action are denoted by numbers. Note: non-steroidal anti-inflammatory drugs (NSAIDs) such as aspirin and ibuprofen inhibit the production of protective prostaglandins by inhibiting cyclooxygenase 1 (COX1). For this reason, NSAIDs can promote ulcer formation, and their antiplatelet effects also make patients more susceptible to excessive bleeding if a gastric ulcer becomes severe. |
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来源 | 自己的作品 |
作者 | Adam L. VanWert, Pharm.D., Ph.D. |
其他版本 | Derivative works of this file: Determinants of Gastric Acid Secretion Edit.svg |
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日期/时间 | 缩略图 | 大小 | 用户 | 备注 | |
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当前 | 2011年1月16日 (日) 11:03 | 1,206 × 829(741 KB) | Vanwa71(留言 | 贡献) | .. | |
2011年1月16日 (日) 10:57 | 1,206 × 829(486 KB) | Vanwa71(留言 | 贡献) | Reverted to version as of 10:39, 16 January 2011 | ||
2011年1月16日 (日) 10:55 | 1,206 × 829(1.33 MB) | Vanwa71(留言 | 贡献) | Linked instead of embedded new graphics last time. | ||
2011年1月16日 (日) 10:39 | 1,206 × 829(486 KB) | Vanwa71(留言 | 贡献) | Reverted to version as of 06:03, 16 January 2011 | ||
2011年1月16日 (日) 10:37 | 1,206 × 829(437 KB) | Vanwa71(留言 | 贡献) | cool effects | ||
2011年1月16日 (日) 06:03 | 1,206 × 829(486 KB) | Vanwa71(留言 | 贡献) | Small detail edits. | ||
2011年1月16日 (日) 05:57 | 1,206 × 829(484 KB) | Vanwa71(留言 | 贡献) | Fixed gastrin and somatostatin flaws | ||
2011年1月16日 (日) 05:14 | 1,206 × 829(472 KB) | Vanwa71(留言 | 贡献) | Forgot categories. | ||
2011年1月16日 (日) 05:11 | 1,206 × 829(472 KB) | Vanwa71(留言 | 贡献) | I finally started using my head, and converted all the text to outlines to keep it exactly as I wanted it. | ||
2011年1月16日 (日) 05:05 | 1,206 × 829(214 KB) | Vanwa71(留言 | 贡献) | Please bear with me, I finally looked up websafe fonts instead of trial and error. Let's hope this works. |
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