Literature DB >> 19490367

Divergent regulation of hypothalamic neuropeptide Y and agouti-related protein by photoperiod in F344 rats with differential food intake and growth.

A W Ross1, C E Johnson, L M Bell, L Reilly, J S Duncan, P Barrett, P D Heideman, P J Morgan.   

Abstract

Hypothalamic genes involved in food intake and growth regulation were studied in F344 rats in response to photoperiod. Two sub-strains were identified: F344/NHsd (F344/N) and F344/NCrHsd (F344/NCr); sensitive and relatively insensitive to photoperiod respectively. In F344/N rats, marked, but opposite, changes in the genes for neuropeptide Y (NPY) (+97.5%) and agouti-related protein (AgRP) (-39.3%) expression in the arcuate nucleus were observed in response to short (8 : 16 h light/dark cycle, SD) relative to long (16 : 8 h light/dark cycle, LD) day photoperiods. Changes were associated with both reduced food intake and growth. Expression of the genes for cocaine and amphetamine-regulated transcript (CART) and pro-opiomelanocortin (POMC) in the arcuate nucleus was unchanged by photoperiod. POMC in the ependymal layer around the third ventricle was markedly inhibited by SD. Parallel decreases in the genes for growth hormone-releasing hormone (GHRH) and somatostatin (Somatostatin) mRNA in the arcuate nucleus and Somatostatin in the periventricular nucleus were observed in SD. Serum levels of insulin-like growth factor (IGF)-1 and insulin were lower in F344/N rats in SD, whereas neither leptin nor corticosterone levels were affected. By contrast, F344/NCr rats that show only minor food intake and growth rate changes showed minimal responses in these genes and hormones. Thus, NPY/AgRP neurones may be pivotal to the photoperiodic regulation of food intake and growth. Potentially, the SD increase in NPY expression may inhibit growth by decreasing GHRH and Somatostatin expression, whereas the decrease in AgRP expression probably leads to reduced food intake. The present study reveals an atypical and divergent regulation of NPY and AgRP, which may relate to their separate roles with respect to growth and food intake, respectively.

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Year:  2009        PMID: 19490367     DOI: 10.1111/j.1365-2826.2009.01878.x

Source DB:  PubMed          Journal:  J Neuroendocrinol        ISSN: 0953-8194            Impact factor:   3.627


  25 in total

1.  Gene expression analysis and microdialysis suggest hypothalamic triiodothyronine (T3) gates daily torpor in Djungarian hamsters (Phodopus sungorus).

Authors:  Jonathan H H Bank; Ceyda Cubuk; Dana Wilson; Eddy Rijntjes; Julia Kemmling; Hanna Markovsky; Perry Barrett; Annika Herwig
Journal:  J Comp Physiol B       Date:  2017-04-01       Impact factor: 2.200

2.  Genetic variation in total number and locations of GnRH neurons identified using in situ hybridization in a wild-source population.

Authors:  Katherine E Kaugars; Charlotte I Rivers; Margaret S Saha; Paul D Heideman
Journal:  J Exp Zool A Ecol Genet Physiol       Date:  2015-12-24

3.  A thyroid hormone challenge in hypothyroid rats identifies T3 regulated genes in the hypothalamus and in models with altered energy balance and glucose homeostasis.

Authors:  Annika Herwig; Gill Campbell; Claus-Dieter Mayer; Anita Boelen; Richard A Anderson; Alexander W Ross; Julian G Mercer; Perry Barrett
Journal:  Thyroid       Date:  2014-09-02       Impact factor: 6.568

4.  Variable proopiomelanocortin expression in tanycytes of the adult rat hypothalamus and pituitary stalk.

Authors:  Gábor Wittmann; Erzsébet Farkas; Anett Szilvásy-Szabó; Balázs Gereben; Csaba Fekete; Ronald M Lechan
Journal:  J Comp Neurol       Date:  2016-09-02       Impact factor: 3.215

Review 5.  Critical determinants of hypothalamic appetitive neuropeptide development and expression: species considerations.

Authors:  B E Grayson; P Kievit; M S Smith; K L Grove
Journal:  Front Neuroendocrinol       Date:  2009-10-12       Impact factor: 8.606

6.  Prss56 expression in the rodent hypothalamus: Inverse correlation with pro-opiomelanocortin suggests oscillatory gene expression in adult rat tanycytes.

Authors:  Gábor Wittmann; Ronald M Lechan
Journal:  J Comp Neurol       Date:  2018-09-22       Impact factor: 3.215

Review 7.  Central somatostatin signaling and regulation of food intake.

Authors:  Andreas Stengel; Yvette Taché
Journal:  Ann N Y Acad Sci       Date:  2019-06-25       Impact factor: 5.691

8.  Patterning of retinoic acid signaling and cell proliferation in the hippocampus.

Authors:  Timothy Goodman; James E Crandall; Sonia E Nanescu; Loredana Quadro; Kirsty Shearer; Alexander Ross; Peter McCaffery
Journal:  Hippocampus       Date:  2012-06-11       Impact factor: 3.899

9.  Thyroid hormone signalling genes are regulated by photoperiod in the hypothalamus of F344 rats.

Authors:  Alexander W Ross; Gisela Helfer; Laura Russell; Veerle M Darras; Peter J Morgan
Journal:  PLoS One       Date:  2011-06-22       Impact factor: 3.240

10.  Hypothalamic ventricular ependymal thyroid hormone deiodinases are an important element of circannual timing in the Siberian hamster (Phodopus sungorus).

Authors:  Annika Herwig; Emmely M de Vries; Matei Bolborea; Dana Wilson; Julian G Mercer; Francis J P Ebling; Peter J Morgan; Perry Barrett
Journal:  PLoS One       Date:  2013-04-18       Impact factor: 3.240

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