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      One Dose of Psilocybin in Late Adolescence Mitigates Deleterious Effects of Developmental Stress on Cognition and Behavioral Despair in Adult Female Rats

      한글로보기

      https://www.riss.kr/link?id=O112952869

      • 저자
      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2020년

      • 작성언어

        -

      • Print ISSN

        0892-6638

      • Online ISSN

        1530-6860

      • 등재정보

        SCI;SCIE;SCOPUS

      • 자료형태

        학술저널

      • 수록면

        1-1   [※수록면이 p5 이하이면, Review, Columns, Editor's Note, Abstract 등일 경우가 있습니다.]

      • 구독기관
        • 전북대학교 중앙도서관  
        • 성균관대학교 중앙학술정보관  
        • 부산대학교 중앙도서관  
        • 전남대학교 중앙도서관  
        • 제주대학교 중앙도서관  
        • 중앙대학교 서울캠퍼스 중앙도서관  
        • 인천대학교 학산도서관  
        • 숙명여자대학교 중앙도서관  
        • 서강대학교 로욜라중앙도서관  
        • 충남대학교 중앙도서관  
        • 한양대학교 백남학술정보관  
        • 이화여자대학교 중앙도서관  
        • 고려대학교 도서관  
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      부가정보

      다국어 초록 (Multilingual Abstract)

      Psilocybin (PSI) has persistent antidepressant efficacy in human trials. We have shown one dose of PSI to significantly decrease depressive‐like behavior in male Wistar‐Kyoto (WKY) rats for at least five weeks without losing efficacy. However, the...

      Psilocybin (PSI) has persistent antidepressant efficacy in human trials. We have shown one dose of PSI to significantly decrease depressive‐like behavior in male Wistar‐Kyoto (WKY) rats for at least five weeks without losing efficacy. However, the outcome assay we used to evaluate depressive‐like behavior, the forced swim test (FST), has been criticized for not providing circuit‐specific endpoint data. Further, rodent strains like WKY selectively bred for face validity in modeling depression have lower translational value than chronic/developmental stress models.
      Pattern separation is a function of the dentate gyrus (DG) and CA3 region of the hippocampus. Pattern separation deficits are measurable in a number of psychological and neurological disorders where the DG‐CA3 circuit is impaired, including major depressive disorder, schizophrenia, and age‐related dementias. The object pattern separation (OPS) task is a new paradigm to measure DG‐CA3 function in rodents, proposed as a cognitive‐based outcome measure for depression‐like phenotypes, but so far only used in healthy male animals. Whether OPS performance correlates with established measures of behavioral despair, or can be normalized by human pharmacotherapies, is unknown.
      Evaluate long‐term antidepressant‐like effects of PSI in the stress‐based adolescent chronic restraint stress (aCRS) model for depression, establish face and predictive validity of the OPS task, and determine whether OPS correlates with FST immobility in aCRS rats.
      Adolescent female Sprague Dawley rats were assigned to groups: not restrained‐saline (NRS), not restrained‐PSI (NRP), restrained‐saline (RS), and restrained‐PSI (RP). RS and RP rats were restrained 1 hr/day post‐natal days (PND) 32–45. Rats received IP PSI (1 mg/kg) or saline PND 52. The OPS task was performed nightly PND 82 (0 cm) – 86 (24 cm) in a 66 cm diameter arena containing two identical objects, one of which was moved from 0 cm to 6, 12, 18, and 24 cm from 0 following an hour intertrial interval. FST was performed PND 89–90.
      Significant discrimination in the OPS at 24 cm was observed in NRS (p<0.001), NRP (p<0.0001), and RP (p<0.01), but RS rats were unable to discriminate between moved and stationary objects. RS rats were significantly more immobile in the FST than NRS rats (p<0.0001). No differences were observed between NRS, NRP, and RP rats. Immobility in the FST was inversely correlated to discrimination in the OPS at 24 cm (r=−0.402, p=0.023).
      The OPS is a translationally relevant outcome with face and predictive validity, correlates with an established measure of depressive‐like behavior, and can be used in female rats.
      One dose of PSI in late adolescence mitigates cognitive and behavioral deficiencies characteristic of the developmentally‐stressed adult aCRS rat model for depression.
      Our aCRS model is uniquely suitable for elucidating the antidepressant mechanisms of PSI, which has translationally relevant antidepressant‐like effects that can be measured using the OPS task, many weeks after administration.
      This work supported by Eleusis, PBC.

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