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      Efferent projections of CGRP/Calca‐expressing parabrachial neurons in mice

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      https://www.riss.kr/link?id=O112742023

      • 저자
      • 발행기관
      • 학술지명
      • 권호사항
      • 발행연도

        2021년

      • 작성언어

        -

      • Print ISSN

        0021-9967

      • Online ISSN

        1096-9861

      • 등재정보

        SCI;SCIE;SCOPUS

      • 자료형태

        학술저널

      • 수록면

        2911-2957   [※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  
        • 계명대학교 동산도서관  
        • 충남대학교 중앙도서관  
        • 한양대학교 백남학술정보관  
        • 이화여자대학교 중앙도서관  
        • 고려대학교 도서관  
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      부가정보

      다국어 초록 (Multilingual Abstract)

      The parabrachial nucleus (PB) is composed of glutamatergic neurons at the midbrain–hindbrain junction. These neurons form many subpopulations, one of which expresses Calca, which encodes the neuropeptide calcitonin gene‐related peptide (CGRP). This Calca‐expressing subpopulation has been implicated in a variety of homeostatic functions, but the overall distribution of Calca‐expressing neurons in this region remains unclear. Also, while previous studies in rats and mice have identified output projections from CGRP‐immunoreactive or Calca‐expressing neurons, we lack a comprehensive understanding of their efferent projections. We began by identifying neurons with Calca mRNA and CGRP immunoreactivity in and around the PB, including populations in the locus coeruleus and motor trigeminal nucleus. Calca‐expressing neurons in the PB prominently express the mu opioid receptor (Oprm1) and are distinct from neighboring neurons that express Foxp2 and Pdyn. Next, we used Cre‐dependent anterograde tracing with synaptophysin‐mCherry to map the efferent projections of these neurons. Calca‐expressing PB neurons heavily target subregions of the amygdala, bed nucleus of the stria terminalis, basal forebrain, thalamic intralaminar and ventral posterior parvicellular nuclei, and hindbrain, in different patterns depending on the injection site location within the PB region. Retrograde axonal tracing revealed that the previously unreported hindbrain projections arise from a rostral‐ventral subset of CGRP/Calca neurons. Finally, we show that these efferent projections of Calca‐expressing neurons are distinct from those of neighboring PB neurons that express Pdyn. This information provides a detailed neuroanatomical framework for interpreting experimental work involving CGRP/Calca‐expressing neurons and opioid action in the PB region.
      The parabrachial nucleus contains Calca‐expressing glutamatergic neurons. We also identified Calca expression in neighboring catecholaminergic neurons in the locus coeruleus. Both populations express Oprm1, which encodes the mu opioid receptor. We trace the overall axonal projections of Calca‐expressing neurons in this region, which complement those of neighboring neurons that express Pdyn. These findings highlight neurons that are potentially important for several aversive symptoms of opioid withdrawal, including malaise, anorexia, nausea, and pain.
      번역하기

      The parabrachial nucleus (PB) is composed of glutamatergic neurons at the midbrain–hindbrain junction. These neurons form many subpopulations, one of which expresses Calca, which encodes the neuropeptide calcitonin gene‐related peptide (CGRP). Thi...

      The parabrachial nucleus (PB) is composed of glutamatergic neurons at the midbrain–hindbrain junction. These neurons form many subpopulations, one of which expresses Calca, which encodes the neuropeptide calcitonin gene‐related peptide (CGRP). This Calca‐expressing subpopulation has been implicated in a variety of homeostatic functions, but the overall distribution of Calca‐expressing neurons in this region remains unclear. Also, while previous studies in rats and mice have identified output projections from CGRP‐immunoreactive or Calca‐expressing neurons, we lack a comprehensive understanding of their efferent projections. We began by identifying neurons with Calca mRNA and CGRP immunoreactivity in and around the PB, including populations in the locus coeruleus and motor trigeminal nucleus. Calca‐expressing neurons in the PB prominently express the mu opioid receptor (Oprm1) and are distinct from neighboring neurons that express Foxp2 and Pdyn. Next, we used Cre‐dependent anterograde tracing with synaptophysin‐mCherry to map the efferent projections of these neurons. Calca‐expressing PB neurons heavily target subregions of the amygdala, bed nucleus of the stria terminalis, basal forebrain, thalamic intralaminar and ventral posterior parvicellular nuclei, and hindbrain, in different patterns depending on the injection site location within the PB region. Retrograde axonal tracing revealed that the previously unreported hindbrain projections arise from a rostral‐ventral subset of CGRP/Calca neurons. Finally, we show that these efferent projections of Calca‐expressing neurons are distinct from those of neighboring PB neurons that express Pdyn. This information provides a detailed neuroanatomical framework for interpreting experimental work involving CGRP/Calca‐expressing neurons and opioid action in the PB region.
      The parabrachial nucleus contains Calca‐expressing glutamatergic neurons. We also identified Calca expression in neighboring catecholaminergic neurons in the locus coeruleus. Both populations express Oprm1, which encodes the mu opioid receptor. We trace the overall axonal projections of Calca‐expressing neurons in this region, which complement those of neighboring neurons that express Pdyn. These findings highlight neurons that are potentially important for several aversive symptoms of opioid withdrawal, including malaise, anorexia, nausea, and pain.

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