Distinct pharmacological mechanisms leading to c-fos gene expression in the fetal suprachiasmatic nucleus
Department of Neurobiology; Weaver Lab
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.
J Biol Rhythms. 2001 Dec;16(6):531-40.
Journal of biological rhythms
Shearman LP, Weaver DR. (2001). Distinct pharmacological mechanisms leading to c-fos gene expression in the fetal suprachiasmatic nucleus. Neurobiology Publications. Retrieved from https://escholarship.umassmed.edu/neurobiology_pp/95