Luminal L-glutamate enhances duodenal mucosal defense mechanisms via multiple glutamate receptors in rats

被引:83
作者
Akiba, Yasutada [1 ,2 ,3 ]
Watanabe, Chikako [2 ,3 ]
Mizumori, Misa [2 ,3 ]
Kaunitz, Jonathan D. [1 ,2 ,3 ]
机构
[1] Greater Los Angeles Vet Affairs Healthcare Syst, Los Angeles, CA USA
[2] Univ Calif Los Angeles, Sch Med, Dept Med, Los Angeles, CA 90024 USA
[3] Brentwood Biomed Res Inst, Los Angeles, CA USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY | 2009年 / 297卷 / 04期
关键词
intracellular alkalinization; mucus secretion; bicarbonate secretion; monosodium glutamate; taste receptor; CALCIUM-SENSING RECEPTOR; MUCUS GEL THICKNESS; BITTER TASTE RECEPTORS; INTRACELLULAR PH; GASTROINTESTINAL-TRACT; CA2+-SENSING RECEPTOR; CARBONIC-ANHYDRASES; CHORDA TYMPANI; BLOOD-FLOW; ACID;
D O I
10.1152/ajpgi.90605.2008
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Akiba Y, Watanabe C, Mizumori M, Kaunitz JD. Luminal L-glutamate enhances duodenal mucosal defense mechanisms via multiple glutamate receptors in rats. Am J Physiol Gastrointest Liver Physiol 297: G781-G791, 2009. First published July 30, 2009; doi: 10.1152/ajpgi.90605.2008.-Presence of taste receptor families in the gastrointestinal mucosa suggests a physiological basis for local and early detection of a meal. We hypothesized that luminal L-glutamate, which is the primary nutrient conferring fundamental umami or proteinaceous taste, influences mucosal defense mechanisms in rat duodenum. We perfused the duodenal mucosa of anesthetized rats with L-glutamate (0.1-10 mM). Intracellular pH (pH(i)) of the epithelial cells, blood flow, and mucus gel thickness (MGT) were simultaneously and continuously measured in vivo. Some rats were pretreated with indomethacin or capsaicin. Duodenal bicarbonate secretion (DBS) was measured with flow-through pH and CO(2) electrodes. We tested the effects of agonists or antagonists for metabotropic glutamate receptor (mGluR) 1 or 4 or calcium-sensing receptor (CaSR) on defense factors. Luminal L-glutamate dose dependently increased pHi and MGT but had no effect on blood flow in the duodenum. L-glutamate (10 mM)-induced cellular alkalinization and mucus secretion were inhibited by pretreatment with indomethacin or capsaicin. L-glutamate effects on pH(i) and MGT were mimicked by mGluR4 agonists and inhibited by an mGluR4 antagonist. CaSR agonists acidified cells with increased MGT and DBS, unlike L-glutamate. Perfusion of L-glutamate with inosinate (inosine 5'-monophosphate, 0.1 mM) enhanced DBS only in combination, suggesting synergistic activation of the L-glutamate receptor, typical of taste receptor type 1. L-leucine or L-aspartate had similar effects on DBS without any effect on pHi and MGT. Preperfusion of L-glutamate prevented acid-induced cellular injury, suggesting that L-glutamate protects the mucosa by enhancing mucosal defenses. Luminal L-glutamate may activate multiple receptors and afferent nerves and locally enhance mucosal defenses to prevent subsequent injury attributable to acid exposure in the duodenum.
引用
收藏
页码:G781 / G791
页数:11
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