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1.
J Pharmacol Sci ; 145(1): 122-129, 2021 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-33357770

RESUMEN

Functional dyspepsia (FD) is thought to be mainly based on gastric motility dysfunction and chronic hypersensitivity, yet FD animal models has been reported a few. We studied to establish the mouse model of impaired gastric motility induced by a pungent ingredient of wasabi allyl isothiocyanate (AITC), which is reliable to evaluate prokinetic agents. Male ddY mice were used. Gastric motility was measured by 13C-acetic acid breath test in conscious mice. AITC (80 mM) was given 60 min before the measurement of motility. Prokinetic agents including itopride (30, 100 mg/kg), mosapride (0.1-1 mg/kg), neostigmine (30 µg/kg), acotiamide (10-100 mg/kg), and daikenchuto (100-1000 mg/kg) were given 40 min before the measurement. AITC impaired gastric motility without mucosal damages, which reverted 24 h after AITC treatment. The decreased motility induced by AITC was restored by prokinetic agents such as itopride, mosapride, neostigmine, and acotiamide. In separate experiment, daikenchuto recovered the decreased motility induced by AITC, although daikenchuto had no effect on motility in normal condition. In conclusion, it is considered that the AITC-induced impaired gastric motility mouse model is useful to develop new prokinetic agents for treatment of FD, and to re-evaluate traditional Japanese herbal medicines.


Asunto(s)
Benzamidas/administración & dosificación , Compuestos de Bencilo/administración & dosificación , Dispepsia/tratamiento farmacológico , Motilidad Gastrointestinal , Isotiocianatos/efectos adversos , Morfolinas/administración & dosificación , Neostigmina/administración & dosificación , Fitoterapia , Extractos Vegetales/administración & dosificación , Tiazoles/administración & dosificación , Wasabia/química , Animales , Benzamidas/farmacología , Compuestos de Bencilo/farmacología , Modelos Animales de Enfermedad , Dispepsia/fisiopatología , Motilidad Gastrointestinal/efectos de los fármacos , Isotiocianatos/aislamiento & purificación , Masculino , Ratones Endogámicos , Morfolinas/farmacología , Neostigmina/farmacología , Panax , Extractos Vegetales/farmacología , Tiazoles/farmacología , Zanthoxylum , Zingiberaceae
2.
Biol Pharm Bull ; 40(9): 1506-1514, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28867733

RESUMEN

Gastric motility disturbance is commonly found in long-standing hyperglycemia. Both delayed and rapid gastric emptying has been reported in diabetes. However, very few studies have followed the changes in gastric emptying during disease progression in diabetes because of technical limitations. 13C-Acetic acid breath test is a validated method which is non-invasive and can be used repeatedly or serially to evaluate gastric emptying changes in animal. We investigated the gastric emptying changes in different stages of diabetes using 13C-acetic acid breath test, as well as its related mechanisms involving interstitial cells of Cajal (ICCs), and stem cell factor (SCF) in streptozotocin-induced diabetic rats. The results showed that gastric emptying was accelerated at the early stage (12 weeks of diabetes) whereas intramuscular ICCs (ICC-IM) networks were not different from normal group. At long-term stage (28 weeks of diabetes), gastric emptying had returned to normal pattern with no delayed. ICC-IM networks were decreased in the diabetic group compared to 12th weeks, and were lower than in the normal group at the same time point. SCF levels were constantly high in the diabetic group than in the normal group. This result indicated that 13C-acetic acid breath test is useful to track the alteration in gastric emptying during disease progression. The change of gastric emptying was not found to be significantly associated with ICC-IM. Elevated SCF may help to preserve ICC-IM, especially in the early phase of diabetes.


Asunto(s)
Ácido Acético/análisis , Pruebas Respiratorias/métodos , Diabetes Mellitus Experimental/fisiopatología , Vaciamiento Gástrico , Animales , Glucemia/análisis , Peso Corporal , Recuento de Células , Diabetes Mellitus Experimental/patología , Progresión de la Enfermedad , Células Intersticiales de Cajal/patología , Masculino , Monitoreo Fisiológico , Proteínas Proto-Oncogénicas c-kit/biosíntesis , Ratas , Ratas Sprague-Dawley , Factor de Células Madre/biosíntesis
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