Literature DB >> 6966962

Ascending components of the medial forebrain bundle from the lower brain stem in the rat, with special reference to raphe and catecholamine cell groups. A study by the HRP method.

H Takagi, S Shiosaka, M Tohyama, E Senba, M Sakanaka.   

Abstract

The afferent connection of the medial forebrain bundle (MFB) arising from the lower brain stem have been investigated by means of horseradish peroxidase (HRP) with sensitive substrate, the injection was made iontophoretically into MFB at various levels. After injection of HRP into MFB, a significant number of HRP-labeled neurons were observed in the following structures of the lower brain stem: (1) raphe nuclear group, (2) locus coeruleus, (3) n. laterodorsalis tegmenti, (4) parabrachial area, (5) A1, A2, A4, A5 and A7 areas where noradrenaline-containing neurons were disseminated, (6) A8, A9 and A10 areas which contain dopamine neurons, (7) surrounding area of the fasciculus longitudinalis medialis at the level of the n. propositus hypoglossi, (8) n. prepositus hypoglossi and (9) mesencephalic gray matter. As a rule, the ascending projections are ipsilateral and course in the medial part of MFB. Regarding the raphe nuclei, we have demonstrated that the caudal raphe nuclei, such as n. raphe magnus and obscurus (but not n. raphe pallidus), also send their axons to the hypothalamus. Particularly, the axons of n. raphe magnus ascend in MFB to reach the level of the preoptic or anterior septal areas. Furthermore, in accordance with previous reports, HRP-labeled cells were also identified in the n. raphe dorsalis, centralis superior and pontis, respectively. It should be further noted that labeled cells appeared in the n. linearis caudalis. In addition, the present study indicates a number of non-aminergic cell groups as sources of ascending mfb fibers. On the whole, the present study further clarified the organization of the components of the MFB ascending from the lower brain stem, and provided some additional anatomical substrates for the physiology of the control of the forebrain by the lower brain stem neurons.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 6966962     DOI: 10.1016/0006-8993(80)90168-7

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  6 in total

Review 1.  Modulation of cardiorespiratory function mediated by the paraventricular nucleus.

Authors:  Prabha Kc; Thomas E Dick
Journal:  Respir Physiol Neurobiol       Date:  2010-08-11       Impact factor: 1.931

Review 2.  Functional topography of midbrain and pontine serotonergic systems: implications for synaptic regulation of serotonergic circuits.

Authors:  Matthew W Hale; Christopher A Lowry
Journal:  Psychopharmacology (Berl)       Date:  2010-11-19       Impact factor: 4.530

3.  Quantitative distribution of rat brain monoamine oxidase A by [14C]clorgyline autoradiography.

Authors:  Y Kondoh; M Murakami; W Yin; S Mizusawa; H Nakamichi; K Nagata
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

Review 4.  Relaxin-3/RXFP3 networks: an emerging target for the treatment of depression and other neuropsychiatric diseases?

Authors:  Craig M Smith; Andrew W Walker; Ihaia T Hosken; Berenice E Chua; Cary Zhang; Mouna Haidar; Andrew L Gundlach
Journal:  Front Pharmacol       Date:  2014-03-21       Impact factor: 5.810

5.  Intranasal administration of a stapled relaxin-3 mimetic has anxiolytic- and antidepressant-like activity in rats.

Authors:  Subhi Marwari; Anders Poulsen; Norrapat Shih; Rajamani Lakshminarayanan; R Manjunatha Kini; Charles William Johannes; Brian William Dymock; Gavin Stewart Dawe
Journal:  Br J Pharmacol       Date:  2019-09-11       Impact factor: 8.739

6.  Fluoxetine-induced recovery of serotonin and norepinephrine projections in a mouse model of post-stroke depression.

Authors:  Amin Zahrai; Faranak Vahid-Ansari; Mireille Daigle; Paul R Albert
Journal:  Transl Psychiatry       Date:  2020-09-30       Impact factor: 6.222

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.