4.5 Article

Projections of nucleus accumbens adenosine A2A receptor neurons in the mouse brain and their implications in mediating sleep-wake regulation

期刊

FRONTIERS IN NEUROANATOMY
卷 7, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fnana.2013.00043

关键词

nucleus accumbens; adeno-associated virus; Cre-Lox; green fluorescent protein; mouse; sleep

资金

  1. National Natural Science Foundation of China [81171299, 31070957, 31171010, 31121061, 31271164, 81271466]
  2. National Basic Research Program of China [2011CB711000]
  3. Shanghai Leading Academic Discipline Project [B119]
  4. Ph.D. Programs Foundation of Ministry of Education of China [20110071110033]
  5. Japan Society for the Promotion of Science [24300129]
  6. World Premier International Research Center Initiative (WPI) from the Ministry of Education, Culture, Sports, Science, and Technology of Japan
  7. Fondation Medicale Reine Elisabeth (Belgium)
  8. FRS-FNRS (Belgium)
  9. FER from ULB
  10. Belgian State-Federal Office for Scientific Affairs [IUTAP - P7/10)]
  11. Action de Recherche Concertee from the Federation Wallonie-Bruxelles
  12. State Key Laboratory of Medical Neurobiology, Fudan University, Shanghai, China
  13. Grants-in-Aid for Scientific Research [25871082] Funding Source: KAKEN

向作者/读者索取更多资源

Adenosine A(2A) receptors (A(2A) Rs) in the nucleus accumbens (Acb) have been demonstrated to play an important role in the arousal effect of adenosine receptor antagonist caffeine, and may be involved in physiological sleep. To better understand the functions of these receptors in sleep, projections of A(2A)R neurons were mapped utilizing adeno-associated virus (AAV) encoding humanized Renilla green fluorescent protein (hrGFP) as a tracer for long axonal pathways. The Cre-dependent AAV was injected into the core (AcbC) and shell (AcbSh) of the Acb in A(2A)R-Cre mice. Immunohistochemistry was then used to visualize hrGFP highlighting the perikarya of the A(2A)R neurons in the injection sites, and their axons in projection regions. The data revealed that A(2A)R neurons exhibit medium-sized and either round or elliptic perikarya with their processes within the Acb. Moreover, the projections from the Acb distributed to nuclei in the forebrain, diencephalon, and brainstem. In the forebrain, A(2A) R neurons from all Acb sub-regions jointly projected to the ventral pallidum, the nucleus of the diagonal band, and the substantia innominata. Heavy projections from the AcbC and the ventral AcbSh, and weaker projections from the medial AcbSh, were observed in the lateral hypothalamus and lateral preoptic area. In the brainstem, the Acb projections were found in the ventral tegmental area, while AcbC and ventral AcbSh also projected to the median raphe nucleus, the dorsal raphe nucleus, and the ventrolateral periaqueductal gray. The results supply a solid base for understanding the roles of the A(2A)R and A(2A)R neurons in the Acb, especially in the regulation of sleep.

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