RISS 학술연구정보서비스

검색
다국어 입력

http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.

변환된 중국어를 복사하여 사용하시면 됩니다.

예시)
  • 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
  • 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
닫기
    인기검색어 순위 펼치기

    RISS 인기검색어

      KCI등재 SCIE SCOPUS

      Depression Promotes the Onset of Irritable Bowel Syndrome through Unique Dysbiosis in Rats = Depression Promotes the Onset of Irritable Bowel Syndrome through Unique Dysbiosis in Rats

      한글로보기

      https://www.riss.kr/link?id=A106264770

      • 0

        상세조회
      • 0

        다운로드
      서지정보 열기
      • 내보내기
      • 내책장담기
      • 공유하기
      • 오류접수

      부가정보

      다국어 초록 (Multilingual Abstract)

      Background/Aims: Although studies using conventional animal models have shown that specific stressors cause irritable bowel syndrome (IBS), it is unclear whether depression itself causes IBS. Our aim was to establish a rat model to determine if depression itself promotes the onset of IBS and to elucidate the role of gut microbiota in brain-gut axis pathogenesis during coincident depression and IBS. Methods: Rat models of depression were induced using our shuttle box method of learned helplessness. Visceral hypersensitivity was evaluated by colorectal distension (CRD) to diagnose IBS. Gut microbiota compositions were analyzed using high-throughput sequencing. In the subanalysis of rats without depression-like symptoms, rats with posttraumatic stress disorder (PTSD) were also examined. Results: The threshold value of CRD in depressed rats was significantly lower than that in control rats. Microbial community analysis of cecal microbiota showed that the relative abundance of Clostridiales incertae sedis, the most prevalent microbe, was significantly lower in depressed rats than in control rats. The distribution pattern of the microbiota clearly differed between depressed rats and control rats. Neither visceral hypersensitivity nor the composition of gut microbiota was altered in rats with PTSD-like phenotypes. Conclusions: Our rat model of depression is useful for clarifying the effect of depression on IBS and suggests that depression itself, rather than specific stressors, promotes the onset of IBS. Further, we provided evidence that various psychiatric diseases, viz., depression and PTSD, are associated with unique gut microbiota profiles, which could differentially affect the onset and progression of coincident IBS. (Gut Liver 2019;13:325-332)
      번역하기

      Background/Aims: Although studies using conventional animal models have shown that specific stressors cause irritable bowel syndrome (IBS), it is unclear whether depression itself causes IBS. Our aim was to establish a rat model to determine if depres...

      Background/Aims: Although studies using conventional animal models have shown that specific stressors cause irritable bowel syndrome (IBS), it is unclear whether depression itself causes IBS. Our aim was to establish a rat model to determine if depression itself promotes the onset of IBS and to elucidate the role of gut microbiota in brain-gut axis pathogenesis during coincident depression and IBS. Methods: Rat models of depression were induced using our shuttle box method of learned helplessness. Visceral hypersensitivity was evaluated by colorectal distension (CRD) to diagnose IBS. Gut microbiota compositions were analyzed using high-throughput sequencing. In the subanalysis of rats without depression-like symptoms, rats with posttraumatic stress disorder (PTSD) were also examined. Results: The threshold value of CRD in depressed rats was significantly lower than that in control rats. Microbial community analysis of cecal microbiota showed that the relative abundance of Clostridiales incertae sedis, the most prevalent microbe, was significantly lower in depressed rats than in control rats. The distribution pattern of the microbiota clearly differed between depressed rats and control rats. Neither visceral hypersensitivity nor the composition of gut microbiota was altered in rats with PTSD-like phenotypes. Conclusions: Our rat model of depression is useful for clarifying the effect of depression on IBS and suggests that depression itself, rather than specific stressors, promotes the onset of IBS. Further, we provided evidence that various psychiatric diseases, viz., depression and PTSD, are associated with unique gut microbiota profiles, which could differentially affect the onset and progression of coincident IBS. (Gut Liver 2019;13:325-332)

      더보기

      참고문헌 (Reference)

      1 Yu M, "Variations in gut microbiota and fecal metabolic phenotype associated with depression by 16S rRNA gene sequencing and LC/MS-based metabolomics" 138 : 231-239, 2017

      2 Caporaso JG, "Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms" 6 : 1621-1624, 2012

      3 Kelly JR, "Transferring the blues : depression-associated gut microbiota induces neurobehavioural changes in the rat" 82 : 109-118, 2016

      4 Koloski NA, "The brain: gut pathway in functional gastrointestinal disorders is bidirectional. A 12-year prospective population-based study" 61 : 1284-1290, 2012

      5 Wakizono T, "Stress vulnerabilities in an animal model of post-traumatic stress disorder" 90 : 687-695, 2007

      6 Kikuchi A, "Relationship between posttraumatic stress disorder-like behavior and reduction of hippocampal 5-bromo-2’-deoxyuridine-positive cells after inescapable shock in rats" 62 : 713-720, 2008

      7 Caporaso JG, "QIIME allows analysis of high-throughput community sequencing data" 7 : 335-336, 2010

      8 Pinto-Sanchez MI, "Probiotic Bifidobacterium longum NCC3001 reduces depression scores and alters brain activity : a pilot study in patients with irritable bowel syndrome" 153 : 448-459, 2017

      9 Aizawa E, "Possible association of Bifidobacterium and Lactobacillus in the gut microbiota of patients with major depressive disorder" 202 : 254-257, 2016

      10 Koba T, "Persistent behavioural changes in rats following inescapable shock stress : a potential model of posttraumatic stress disorder" 2 : 34-37, 2001

      1 Yu M, "Variations in gut microbiota and fecal metabolic phenotype associated with depression by 16S rRNA gene sequencing and LC/MS-based metabolomics" 138 : 231-239, 2017

      2 Caporaso JG, "Ultra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms" 6 : 1621-1624, 2012

      3 Kelly JR, "Transferring the blues : depression-associated gut microbiota induces neurobehavioural changes in the rat" 82 : 109-118, 2016

      4 Koloski NA, "The brain: gut pathway in functional gastrointestinal disorders is bidirectional. A 12-year prospective population-based study" 61 : 1284-1290, 2012

      5 Wakizono T, "Stress vulnerabilities in an animal model of post-traumatic stress disorder" 90 : 687-695, 2007

      6 Kikuchi A, "Relationship between posttraumatic stress disorder-like behavior and reduction of hippocampal 5-bromo-2’-deoxyuridine-positive cells after inescapable shock in rats" 62 : 713-720, 2008

      7 Caporaso JG, "QIIME allows analysis of high-throughput community sequencing data" 7 : 335-336, 2010

      8 Pinto-Sanchez MI, "Probiotic Bifidobacterium longum NCC3001 reduces depression scores and alters brain activity : a pilot study in patients with irritable bowel syndrome" 153 : 448-459, 2017

      9 Aizawa E, "Possible association of Bifidobacterium and Lactobacillus in the gut microbiota of patients with major depressive disorder" 202 : 254-257, 2016

      10 Koba T, "Persistent behavioural changes in rats following inescapable shock stress : a potential model of posttraumatic stress disorder" 2 : 34-37, 2001

      11 Kanazawa M, "Patients and nonconsulters with irritable bowel syndrome reporting a parental history of bowel problems have more impaired psychological distress" 49 : 1046-1053, 2004

      12 Jinno S, "Maternal prebiotic ingestion increased the number of fecal bifidobacteria in pregnant women but not in their neonates aged one month" 9 : E196-, 2017

      13 Ludidi S, "Markers for visceral hypersensitivity in patients with irritable bowel syndrome" 26 : 1104-1111, 2014

      14 Keszthelyi D, "Irritable bowel syndrome:methods, mechanisms, and pathophysiology. Methods to assess visceral hypersensitivity in irritable bowel syndrome" 303 : G141-G154, 2012

      15 Gwee KA, "Irritable bowel syndrome in Asia : pathogenesis, natural history, epidemiology, and management" 33 : 99-110, 2018

      16 Fung TC, "Interactions between the microbiota, immune and nervous systems in health and disease" 20 : 145-155, 2017

      17 Tap J, "Identification of an intestinal microbiota signature associated with severity of irritable bowel syndrome" 152 : 111-123, 2017

      18 Mosca A, "Gut microbiota diversity and human diseases : should we reintroduce key predators in our ecosystem" 7 : 455-, 2016

      19 Dalziel JE, "Gastroparesis and lipid metabolism-associated dysbiosis in Wistar-Kyoto rats" 313 : G62-, 2017

      20 Zhang L, "Exogenous interleukin-6 facilitated the contraction of the colon in a depression rat model" 58 : 2187-2196, 2013

      21 Takahashi T, "Environmental enrichment enhances autophagy signaling in the rat hippocampus" 1592 : 113-123, 2014

      22 Overmier JB, "Effects of inescapable shock upon subsequent escape and avoidance responding" 63 : 28-33, 1967

      23 Sawamura T, "Effect of paroxetine on a model of posttraumatic stress disorder in rats" 357 : 37-40, 2004

      24 Labus JS, "Differences in gut microbial composition correlate with regional brain volumes in irritable bowel syndrome" 5 : 49-, 2017

      25 Musty RE, "Criterion for learned helplessness in the rat : a redefinition" 36 : 739-744, 1990

      26 Grenham S, "Brain-gut-microbe communication in health and disease" 2 : 94-, 2011

      27 Park AJ, "Altered colonic function and microbiota profile in a mouse model of chronic depression" 25 : 733-, 2013

      28 Rodiño-Janeiro BK, "A review of microbiota and irritable bowel syndrome : future in therapies" 35 : 289-310, 2018

      29 Al-Chaer ED, "A new model of chronic visceral hypersensitivity in adult rats induced by colon irritation during postnatal development" 119 : 1276-1285, 2000

      30 Lima-Ojeda JM, ""I am I and my bacterial circumstances" : linking gut microbiome, neurodevelopment, and depression" 8 : 153-, 2017

      더보기

      동일학술지(권/호) 다른 논문

      분석정보

      View

      상세정보조회

      0

      Usage

      원문다운로드

      0

      대출신청

      0

      복사신청

      0

      EDDS신청

      0

      동일 주제 내 활용도 TOP

      더보기

      주제

      연도별 연구동향

      연도별 활용동향

      연관논문

      연구자 네트워크맵

      공동연구자 (7)

      유사연구자 (20) 활용도상위20명

      인용정보 인용지수 설명보기

      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-02-25 학회명변경 한글명 : 거트앤리버 발행위원회 -> 거트앤리버 소화기연관학회협의회 KCI등재
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2013-10-01 평가 등재학술지 선정 (기타) KCI등재
      2012-01-01 평가 등재후보학술지 유지 (기타) KCI등재후보
      2011-01-01 평가 등재후보 1차 FAIL (등재후보1차) KCI등재후보
      2009-01-01 평가 SCIE 등재 (신규평가) KCI등재후보
      더보기

      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 2.29 0.44 1.5
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      1.21 1.02 0.46 0.28
      더보기

      이 자료와 함께 이용한 RISS 자료

      나만을 위한 추천자료

      해외이동버튼