2003 Fiscal Year Final Research Report Summary
Regulation of hypothalamic-pituitary-adrenal system for stress response by intestinal microbiota
Project/Area Number |
13470014
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Environmental physiology (including Physical medicine and Nutritional physiology)
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Research Institution | Kyushu University |
Principal Investigator |
KUBO Chiharu Kyushu University, Graduate School of Medical Sciences, Prof., 大学院・医学研究院, 教授 (80117100)
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Co-Investigator(Kenkyū-buntansha) |
KOGA Yasuhiro Tokai University School of Medicine, Prof., 医学部, 教授 (60170221)
SUDO Nobuyuki Kyushu University, Graduate School of Medical Sciences, Assoc.Prof., 大学院・医学研究院, 助教授 (60304812)
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Project Period (FY) |
2001 – 2003
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Keywords | Intestinal microbiota / Stress / Hypothalamic-pituitary-adrenal axis / Germ-free mouse |
Research Abstract |
Indigenous microbiota have several beneficial effects on host physiological functions ; however, little is known about whether or not postnatal microbial colonization can affect the development of brain plasticity and a subsequent physiological system response. To test the idea that such microbes may affect the development of neural systems that govern endocrine response to stress, we investigated hypothalamic-pituitary-adrenal(HPA) reaction to stress by comparing germfree(GF), specific pathogen free (SPF), and gnotobiotic mice. Plasma ACTH and corticosterone elevation in response to restraint stress was substantially higher in GF mice than in SPF mice, but not by ether stimulus. Moreover, GF mice also exhibited reduced brain-derived neurotrophic factor expression levels in the cortex and hippocampus relative to SPF mice. The exaggerated HPA stress response by GF mice was reversed by reconstitution with Bifidobacterium infantis. In contrast, monoassociation with enteropathogenic Escherichia coli, but not with its mutant strain devoid of the translocated intimin receptor gene, enhanced such a response to stress. Importantly, the enhanced HPA response of GF mice was partially corrected by reconstitution with SPF feces at an early stage, but not by any reconstitution exerted at a later stage, which thus indicates that exposure to microbes at an early developmental stage is required for the HPA system to become fully susceptible to inhibitory neural regulation. These results suggest that commensal microbiota can affect the postnatal development of HPA stress response in mice.
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Research Products
(8 results)