Literature DB >> 8358602

Intracerebroventricular administration of corticotropin-releasing factor induces c-fos mRNA expression in brain regions related to stress responses: comparison with pattern of c-fos mRNA induction after stress.

T Imaki1, T Shibasaki, M Hotta, H Demura.   

Abstract

Centrally administered corticotropin-releasing factor (CRF) produces a number of physiological and behavioral changes akin to those elicited by exposure to acute stress. However, the specific brain site of action responsible for the centrally activating property of CRF has not been precisely determined. In this study, we used in situ hybridization histochemistry for c-fos mRNA to map potential neuronal structures activated after intracerebroventricular (i.c.v.) injection of CRF and compared the distribution of c-fos mRNA with that after stress. Wistar male rats were sacrificed 30, 60, 120 and 180 min after the i.c.v. injection of 1 microgram ovine CRF or vehicle alone. Another group of rats was exposed to immobilization stress for 60 min or electrical foot-shock stress (1.5 mA, 1-s duration, 30 x) for 15 min and sacrificed before and 30, 60, 120 and 180 min after the beginning of stress. Centrally administered CRF rapidly (30-60 min) induced c-fos mRNA expression in most of the areas that showed hybridization signals for c-fos after stress: the limbic structures, including the piriform cortex, cingulate cortex, the lateral septal nucleus, the hippocampus, the anterior corticomedial and the medial amygdaloid nuclei, the hypothalamic nuclei, such as the paraventricular nucleus, the supraoptic nucleus (SO) and the dorsomedial nucleus (DMD), and some brainstem nuclei like the pontine nucleus, the locus ceruleus (LC) and Barrington's nucleus. The granular layer of the cerebellum, some thalamic nuclei and the habenula also showed hybridization signals after i.c.v. injection of CRF and stress. However, c-fos induction in the bed nucleus of the stria terminalis, the central nucleus of the amygdala (CeA) and the nucleus tractus solitarius (SOL) was seen only after i.c.v. administration of CRF; in the septo-hypothalamic nucleus and the superior olive, however, c-fos mRNA expression was observed only after stress. There were no differences in the pattern of c-fos mRNA expression between the two stress paradigms. In contrast, i.c.v. injection of saline-induced expression of c-fos mRNA in the piriform cortex, neocortex, cingulate cortex and the amygdala was much less than that seen after i.c.v.-administered CRF as evident in the intensity of the signals. These results suggest that CRF produces c-fos mRNA expression in the brain areas related to stress response, and that CRF may induce behavioral and neuroendocrine responses through activating these brain structures, such as the limbic system and the hypothalamic nuclei.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8358602     DOI: 10.1016/0006-8993(93)90199-w

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


  35 in total

1.  Cannabinoid CB1 receptors mediate the effects of corticotropin-releasing factor on the reinstatement of cocaine seeking and expression of cocaine-induced behavioural sensitization.

Authors:  D A Kupferschmidt; P G Klas; S Erb
Journal:  Br J Pharmacol       Date:  2012-09       Impact factor: 8.739

Review 2.  Chronic alcohol neuroadaptation and stress contribute to susceptibility for alcohol craving and relapse.

Authors:  George R Breese; Rajita Sinha; Markus Heilig
Journal:  Pharmacol Ther       Date:  2010-10-15       Impact factor: 12.310

3.  Teneurin C-terminal associated peptide-1 blocks the effects of corticotropin-releasing factor on reinstatement of cocaine seeking and on cocaine-induced behavioural sensitization.

Authors:  David A Kupferschmidt; David A Lovejoy; Susan Rotzinger; Suzanne Erb
Journal:  Br J Pharmacol       Date:  2011-02       Impact factor: 8.739

4.  Long-term, progressive hippocampal cell loss and dysfunction induced by early-life administration of corticotropin-releasing hormone reproduce the effects of early-life stress.

Authors:  K L Brunson; M Eghbal-Ahmadi; R Bender; Y Chen; T Z Baram
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-10       Impact factor: 11.205

5.  Predator threat induces behavioral inhibition, pituitary-adrenal activation and changes in amygdala CRF-binding protein gene expression.

Authors:  Patrick H Roseboom; Steven A Nanda; Vaishali P Bakshi; Andrea Trentani; Sarah M Newman; Ned H Kalin
Journal:  Psychoneuroendocrinology       Date:  2006-11-20       Impact factor: 4.905

6.  Social recognition memory requires two stages of protein synthesis in mice.

Authors:  Karin Richter; Gerald Wolf; Mario Engelmann
Journal:  Learn Mem       Date:  2005 Jul-Aug       Impact factor: 2.460

Review 7.  Hippocampal neuroplasticity induced by early-life stress: functional and molecular aspects.

Authors:  Kristina A Fenoglio; Kristen L Brunson; Tallie Z Baram
Journal:  Front Neuroendocrinol       Date:  2006-04-17       Impact factor: 8.606

8.  Ferret odor as a processive stress model in rats: neurochemical, behavioral, and endocrine evidence.

Authors:  C V Masini; S Sauer; S Campeau
Journal:  Behav Neurosci       Date:  2005-02       Impact factor: 1.912

9.  Sex differences in corticotropin releasing factor-evoked behavior and activated networks.

Authors:  Kimberly R Wiersielis; Brittany Wicks; Hannah Simko; Sarah R Cohen; Sabina Khantsis; Nausheen Baksh; David E Waxler; Debra A Bangasser
Journal:  Psychoneuroendocrinology       Date:  2016-07-28       Impact factor: 4.905

10.  Type 1 corticotropin-releasing factor receptor expression reported in BAC transgenic mice: implications for reconciling ligand-receptor mismatch in the central corticotropin-releasing factor system.

Authors:  Nicholas J Justice; Zung Fan Yuan; Paul E Sawchenko; Wylie Vale
Journal:  J Comp Neurol       Date:  2008-12-01       Impact factor: 3.215

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.