Literature DB >> 20447445

The effect of prenatal nicotine exposure on PDGFR-mediated anti-apoptotic mechanism in the caudal brainstem of developing rat.

Narong Simakajornboon1, Teeradej Kuptanon, Piyawat Jirapongsuwan.   

Abstract

Maternal cigarette smoking is a major risk factor for sudden infant death syndrome (SIDS); however, the mechanism underlying this association is currently unknown. Prenatal nicotine exposure is accompanied by a decrease in the magnitude of hypoxic ventilatory depression, the component of hypoxic ventilatory response that activates the PDGF-beta receptor (PDGFR) and its downstream anti-apoptotic cascade in the caudal brainstem (CB) of developing rats. In this study, we evaluated the effect of prenatal nicotine exposure on PDGFR activation and the subsequent activation of downstream anti-apoptotic processes through the Akt/BAD pathway. The 5-day timed-pregnant Sprague-Dawley rats underwent surgical implantation of an osmotic pump containing either normal saline (control) or a solution of nicotine tartrate. The CB was harvested from 5-day-old rat pups (n=8-10 for each time point) in each group after exposure to normoxia or hypoxic challenges with 10% O(2) for 5, 15, 30, 60 or 120 min. Immunoprecipitation and immunoblots of CB lysates revealed phosphorylation of PDGFR, Akt and BAD-136 during hypoxia in control pups. Prenatal nicotine exposure was associated with attenuation of these responses at all time points. Analysis of an early apoptotic marker in the CB revealed that activation of cleaved caspase-3 occurred only at 120 min of hypoxic exposure in the control. Prenatal nicotine exposure accelerated this response, causing early activation at 30 and 60 min. We conclude that prenatal nicotine exposure attenuates the phosphorylation of PDGFR, Akt and Bad-136 during hypoxia in the CB of developing rats. This modulation of anti-apoptotic cascades accelerates activation of the early apoptotic marker. We speculate that prenatal nicotine exposure affects apoptosis in the CB of developing animals and may increase the vulnerability of neural cells in the respiratory control area, a process that may underlie the association between maternal smoking and SIDS. (c) 2010 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20447445     DOI: 10.1016/j.neulet.2010.04.067

Source DB:  PubMed          Journal:  Neurosci Lett        ISSN: 0304-3940            Impact factor:   3.046


  2 in total

1.  KCTD8 gene and brain growth in adverse intrauterine environment: a genome-wide association study.

Authors:  Tomás Paus; Manon Bernard; M Mallar Chakravarty; George Davey Smith; Jesse Gillis; Anbarasu Lourdusamy; Melkaye G Melka; Gabriel Leonard; Paul Pavlidis; Michel Perron; G Bruce Pike; Louis Richer; Gunter Schumann; Nicholas Timpson; Roberto Toro; Suzanne Veillette; Zdenka Pausova
Journal:  Cereb Cortex       Date:  2011-12-09       Impact factor: 5.357

2.  Japanese encephalitis virus induces matrix metalloproteinase-9 expression via a ROS/c-Src/PDGFR/PI3K/Akt/MAPKs-dependent AP-1 pathway in rat brain astrocytes.

Authors:  Chuen-Mao Yang; Chih-Chung Lin; I-Ta Lee; Yi-Hsin Lin; Caleb M Yang; Wei-June Chen; Mei-Jie Jou; Li-Der Hsiao
Journal:  J Neuroinflammation       Date:  2012-01-18       Impact factor: 8.322

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.