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DOI 10.1254/jphs.09r08fm

Медицинская библиотека · Journal of pharmacological sciences · 2010

New frontiers in gut nutrient sensor research: monosodium L-glutamate added to a high-energy, high-protein liquid diet promotes gastric emptying: a possible therapy for patients with functional dyspepsia.

Kusano Motoyasu, Zai Hiroaki, Hosaka Hiroko, Shimoyama Yasuyuki, Nagoshi Atsuto, Maeda Masaki, Kawamura Osamu, Mori Masatomo

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Аннотация

Functional dyspepsia is a clinical syndrome that features abdominal symptoms centered in the upper abdomen without an organic basis. Three possible mechanisms of gastric dysfunction could be related to functional dyspepsia: 1) delayed gastric emptying, 2) impaired gastric accommodation to food intake, and 3) hypersensitivity to gastric distention. Delayed gastric emptying has been suggested to lead to prolonged antral distension that causes dyspeptic symptoms. Delayed gastric emptying is therefore a focal point of debate about anorexia caused by dyspepsia, and prokinetic agents are often administered in Japan for its treatment. Recently, we found that addition of monosodium L-glutamate (MSG) to a high-energy liquid diet rich in casein promoted gastric emptying in healthy men. Therefore, another potential method to improve delayed gastric emptying could be enhancement of chemosensors that activate the autonomic nervous system innervating the gastrointestinal tract. In conclusion, enrichment with glutamate promoted gastric emptying after intake of a high-protein meal, suggesting that free glutamate is important for protein digestion and that MSG may be helpful for management of delayed gastric emptying in patients with functional dyspepsia.

Для цитирования: Kusano Motoyasu, Zai Hiroaki, Hosaka Hiroko, Shimoyama Yasuyuki, Nagoshi Atsuto, Maeda Masaki, Kawamura Osamu, Mori Masatomo. New frontiers in gut nutrient sensor research: monosodium L-glutamate added to a high-energy, high-protein liquid diet promotes gastric emptying: a possible therapy for patients with functional dyspepsia.. Journal of pharmacological sciences. 2010. DOI: 10.1254/jphs.09r08fm.

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