Utility of animal gastrointestinal motility and transit models in functional gastrointestinal disorders
被引:10
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作者:
Al-Saffar, Ahmad
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Uppsala Univ Hosp, Dept Med Sci Gastroeneterol & Hepatol, S-75185 Uppsala, SwedenUppsala Univ Hosp, Dept Med Sci Gastroeneterol & Hepatol, S-75185 Uppsala, Sweden
Al-Saffar, Ahmad
[1
]
Takemi, Shota
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机构:
Saitama Univ, Grad Sch Sci & Engn, Div Life Sci, Area Regulatory Biol,Sakura Ku, 255 Shimo Ohkubo, Saitama 3388570, JapanUppsala Univ Hosp, Dept Med Sci Gastroeneterol & Hepatol, S-75185 Uppsala, Sweden
机构:
Saitama Univ, Grad Sch Sci & Engn, Div Life Sci, Area Regulatory Biol,Sakura Ku, 255 Shimo Ohkubo, Saitama 3388570, JapanUppsala Univ Hosp, Dept Med Sci Gastroeneterol & Hepatol, S-75185 Uppsala, Sweden
Sakata, Ichiro
[2
]
Sakai, Takafumi
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Saitama Univ, Grad Sch Sci & Engn, Div Life Sci, Area Regulatory Biol,Sakura Ku, 255 Shimo Ohkubo, Saitama 3388570, Japan
Saitama Univ, Grad Sch Sci & Engn, Div Strategy Res, Area Life NanoBio,Sakura Ku, 255 Shimo Ohkubo, Saitama 3388570, JapanUppsala Univ Hosp, Dept Med Sci Gastroeneterol & Hepatol, S-75185 Uppsala, Sweden
Sakai, Takafumi
[2
,4
]
机构:
[1] Uppsala Univ Hosp, Dept Med Sci Gastroeneterol & Hepatol, S-75185 Uppsala, Sweden
[2] Saitama Univ, Grad Sch Sci & Engn, Div Life Sci, Area Regulatory Biol,Sakura Ku, 255 Shimo Ohkubo, Saitama 3388570, Japan
Alteration in the gastrointestinal (GI) motility and transit comprises an important component of the functional gastrointestinal disorders (FGID). Available animal GI motility and transit models are to study symptoms (delayed gastric emptying, constipation, diarrhea) rather than biological markers to develop an effective treatment that targets the underlying mechanism of altered GI motility in patients. Animal data generated from commonly used methods in human like scintigraphy, breath test and wireless motility capsule may directly translate to the clinic. However, species differences in the control mechanism or pharmacological responses of GI motility may compromise the predictive and translational value of the preclinical data to human. In this review we aim to provide a summary on animal models used to mimic GI motility alteration in FGID, and the impact of the species differences in the physiological and pharmacological responses on the translation of animal GI motility and transit data to human. (C) 2019 Elsevier Ltd. All rights reserved.
机构:
Columbia Univ, Irving Med Ctr, Morgan Stanley Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, 3959 Braodway CHN7, New York, NY 10032 USAColumbia Univ, Irving Med Ctr, Morgan Stanley Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, 3959 Braodway CHN7, New York, NY 10032 USA
Miller, Jonathan
Khlevner, Julie
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机构:
Columbia Univ, Irving Med Ctr, Morgan Stanley Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, 3959 Braodway CHN7, New York, NY 10032 USAColumbia Univ, Irving Med Ctr, Morgan Stanley Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, 3959 Braodway CHN7, New York, NY 10032 USA
Khlevner, Julie
Rodriguez, Leonel
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机构:
Yale Univ, Sch Med, Yale New Haven Childrens Hosp, Sect Pediat Gastroenterol Hepatol & Nutr, 333 Cedar St,LMP 4093, New Haven, CT 06510 USAColumbia Univ, Irving Med Ctr, Morgan Stanley Childrens Hosp, Div Pediat Gastroenterol Hepatol & Nutr, 3959 Braodway CHN7, New York, NY 10032 USA