Distinct pharmacological mechanisms leading to c-fos gene expression in the fetal suprachiasmatic nucleus

UMMS Affiliation

Department of Neurobiology; Weaver Lab



Document Type


Medical Subject Headings

2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine; Adenosine; Animals; Caffeine; Central Nervous System Stimulants; Dizocilpine Maleate; Female; Gene Expression Regulation; Genes, fos; Image Processing, Computer-Assisted; In Situ Hybridization; Pregnancy; RNA, Messenger; Rats; Rats, Sprague-Dawley; Receptors, Cell Surface; Suprachiasmatic Nucleus


Neuroscience and Neurobiology


Maternal treatment with cocaine or a D1-dopamine receptor agonist induces c-fos gene expression in the fetal suprachiasmatic nuclei (SCN). Other treatments that induce c-fos expression in the fetal SCN include caffeine and nicotine. In the current article, the authors assessed whether these different pharmacological treatments activate c-fos expression by a common neurochemical mechanism. The results indicate the presence of at least two distinct pharmacological pathways to c-fos expression in the fetal rat SCN. Previous studies demonstrate that prenatal activation of dopamine receptors affects the developing circadian system. The present work shows that stimulant drugs influence the fetal brain through multiple transmitter systems and further suggests that there may be multiple pathways leading to entrainment of the fetal biological clock.

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Citation: J Biol Rhythms. 2001 Dec;16(6):531-40.

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Link to Article in PubMed

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