Research reportModulation of catecholamine turnover rate in brain regions of rats exposed prenatally to morphine
References (33)
- et al.
Ontological development of opiate receptors in rodent brain
Brain Res.
(1976) The development of catecholaminergic neurons of the central nervous system
Neurosci. Res.
(1973)Benzodiazepines: influence on developing brain
Prog. Brain Res.
(1988)- et al.
Release of [3H]norepinephrine: alteration by early developmental exposure to diazepam
Brain Res.
(1986) - et al.
An ontogenetic study on the effect of catecholamine receptor-stimulating agents on the turnover of norepinephrine and dopamine in the brain
Brain Res.
(1974) The postnatal ontogeny of monoamine containing neurons in the central nervous system of the albino rat
Brain Res.
(1972)- et al.
Protein measurement with the Folin phenol reagent
J. Biol. Chem.
(1951) - et al.
Perinatal cocaine and methamphethamine exposure: maternal and neonatal correlates
J. Pediatr.
(1987) - et al.
Prenatal diazepam exposure in rats: long-lasting, receptor-mediated effects on hypothalamic norepinephrine-containing neurons
Brain Res.
(1984) - et al.
Prenatal exposure to diazepam alters central and peripheral responses to stress in adult rat offspring
Brain Res.
(1984)
Effects of prenatal morphine sulfate on reproductive function of female rats
Pharmacol. Biochem. Behav.
Effects of prenatal exposure to morphine on the development of sexual behavior in rats
Pharmacol. Biochem. Behav.
Effects of prenatal morphine on adult sexual behavior and brain catecholamines in rats
Dev. Brain Res.
Sexually dimorphic effects of prenatal cocaine on adult sexual behavior and brain catecholamines in rats
Dev. Brain Res.
Androgen and estrogen receptors in embryonic and neonatal rat brain
Dev. Brain Res.
Changes in monoamines of rat brain during postnatal ontogeny
Biochim. Biophys. Acta
Cited by (58)
Opioid withdrawal behavior in spiny mice: A novel preclinical model of neonatal opioid withdrawal syndrome (NOWS)
2021, HeliyonCitation Excerpt :Following prenatal morphine exposure, an increase in hypothalamic levels of norepinephrine and rate of turnover was observed in male rats. Whereas, females were found to have decreased levels of hypothalamic norepinephrine and turnover rate (Vathy et al., 1994). Additionally, previous studies have found that in untreated mice, males have been shown to emit a greater number of USV's compared to females (Bowers et al., 2013).
Early life opioid exposure and potential long-term effects
2019, Neurobiology of StressDetour behavior changes associated with prenatal morphine exposure in 11-day-old chicks
2010, International Journal of Developmental NeuroscienceCitation Excerpt :One of the key neurochemical mediators of stress responses in the CNS is norepinephrine (NE) (Glavin, 1985). Series of studies by Vathy and co-workers (Rimanoczy and Vathy, 1995; Vathy, 1995; Vathy and Katay, 1992; Vathy et al., 1994) consistently demonstrate that exposure of pregnant rats to morphine during mid to late gestation induces long-term, sex-specific alterations in the opioid and NE systems of the exposed adult progeny. Furthermore, those long-term alternations are localized in several brain regions known to participate in the regulation of stress responses and the maintenance of homeostatic balance between the external environment, the brain and the rest of the body (Vathy, 2002).
Is the brain hormonally imprintable?
2005, Brain and Development