RESUMO
Smaller hippocampal volume is associated with psychiatric disorders. Variations in hippocampal volume are discussed as both a consequence of the neurotoxic effects of stress and as a pre-existing condition leading to increased vulnerability for cognitive and emotional impairments. To investigate whether early experience can account for variability in hippocampal volume in adulthood (vulnerability hypothesis), we assessed the relationship between birth weight and hippocampal volume in 44 subjects. The reported quality of maternal care in early childhood, as evaluated by the Parental Bonding Inventory, was used as index of the quality of the postnatal environment. Hippocampal volume was assessed from magnetic resonance images using a manual segmentation protocol. We show that birth weight significantly predicts hippocampal volume in adulthood only in female subjects reporting low maternal care. The results suggest that the postnatal environment modulates the neurodevelopmental consequences of prenatal risk and that this effect is sex-specific.
Assuntos
Educação Infantil , Hipocampo/anatomia & histologia , Hipocampo/embriologia , Mães , Fatores Sexuais , Estresse Fisiológico/embriologia , Adulto , Peso ao Nascer , Criança , Desenvolvimento Embrionário , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Prognóstico , Fatores de RiscoRESUMO
Optimal functioning of the hypothalamo-pituitary-adrenal (HPA) axis is paramount to maximizing fitness in vertebrates. Research in laboratory mammals has suggested that maternally-induced stress can cause significant variation in the responsiveness of an offspring's HPA axis involving both pre- and post-natal developmental mechanisms. However, very little is known regarding effects of maternal stress on the variability of offspring adrenocortical functioning in free-living vertebrates. Here we use an experimental approach that independently lowers the quality of both the pre- and post-natal developmental environment to examine programming and plasticity in the responsiveness of the HPA axis in fledglings of a free-living passerine, the European starling (Sturnus vulgaris). We found that mimicking a hormonal signal of poor maternal condition via an experimental pre-natal increase in yolk corticosterone decreased the subsequent responsiveness of the HPA axis in fledglings. Conversely, decreasing the quality of the post-natal developmental environment (by decreasing maternal provisioning capability via a maternal feather-clipping manipulation) increased subsequent responsiveness of the HPA axis in fledglings, apparently through direct effects on nestling body condition. The plasticity of these responses was sex-specific with smaller female offspring showing the largest increase in HPA reactivity. We suggest that pre-natal, corticosterone-induced, plasticity in the HPA axis may be a 'predictive adaptive response' (PAR): a form of adaptive developmental plasticity where the advantage of the induced phenotype is manifested in a future life-history stage. Further, we introduce a new term to define the condition-driven post-natal plasticity of the HPA axis to an unpredictable post-natal environment, namely a 'reactive adaptive response' (RAR). This study confirms that the quality of both the pre- and post-natal developmental environment can be a significant source of variation in the responsiveness of the HPA axis, and provides a frame-work for examining ecologically-relevant sources of stress-induced programming and plasticity in this endocrine system in a free-living vertebrate, respectively.
Assuntos
Sistema Hipotálamo-Hipofisário/fisiologia , Plasticidade Neuronal/fisiologia , Estorninhos/embriologia , Estorninhos/crescimento & desenvolvimento , Estresse Fisiológico/fisiopatologia , Animais , Animais Selvagens/embriologia , Animais Selvagens/crescimento & desenvolvimento , Animais Selvagens/metabolismo , Animais Selvagens/fisiologia , Tamanho da Ninhada , Corticosterona/sangue , Corticosterona/metabolismo , Corticosterona/farmacologia , Embrião não Mamífero/efeitos dos fármacos , Reação de Fuga/efeitos dos fármacos , Reação de Fuga/fisiologia , Feminino , Manobra Psicológica , Sistema Hipotálamo-Hipofisário/efeitos dos fármacos , Sistema Hipotálamo-Hipofisário/metabolismo , Masculino , Exposição Materna/efeitos adversos , Mães , Comportamento de Nidação/fisiologia , Plasticidade Neuronal/efeitos dos fármacos , Estorninhos/metabolismo , Estorninhos/fisiologia , Estresse Fisiológico/sangue , Estresse Fisiológico/embriologia , Estresse Fisiológico/metabolismoRESUMO
Plasma ACTH and corticosteroid concentrations were measured by radioimmunoassay in chronically catheterized fetuses of 32 pregnant sheep. Fetal plasma ACTH levels 38+/-5 pg/ml (means+/-SEM) were slightly (P < 0.05) lower than maternal 54+/-4 pg/ml levels. No general rise in fetal plasma ACTH concentration was noted before 140 days gestation; however, fetal plasma corticoid levels began to increase after about 125 days. This suggested that an increase in fetal adrenal responsiveness to endogenous ACTH occurred during gestation. Hemorrhage of 15% of estimated blood volume decreased mean arterial pressure from 54+/-3 to 36+/-3 torr and increased plasma ACTH from 30+/-5 to 130+/-30 pg/ml in fetuses older than 0.80 gestation. In fetuses younger than 0.67 gestation, 15% hemorrhage caused no change in plasma ACTH levels despite a significant fall in mean arterial pressure. This suggests that system(s) subserving the ACTH response to mild hemorrhage are either absent or nonfunctional in the younger fetuses. The hemorrhage-induced increase in plasma ACTH levels was associated with a small rise in plasma corticoids in fetuses younger than 0.94 gestation. In older fetuses, a similar increase in plasma ACTH was associated with a pronounced increase in plasma corticoid levels. This also suggests that an increase in adrenal responsiveness to endogenous ACTH occurs during gestation. No detectable changes in maternal plasma ACTH or corticoids were found in response to fetal hemorrhage, thus the fetal pituitary-adrenal axis can autonomously respond to stress.
Assuntos
Doenças Fetais/embriologia , Hemorragia/embriologia , Sistema Hipófise-Suprarrenal/embriologia , Estresse Fisiológico/embriologia , Corticosteroides/sangue , Hormônio Adrenocorticotrópico/sangue , Animais , Feminino , Doenças Fetais/sangue , Hemorragia/sangue , Gravidez , Ovinos , Estresse Fisiológico/sangueRESUMO
Table II summarizes in tabular form the major features of the fetal endocrine milieu discussed in the foregoing pages. The mammalian fetus develops in an environment where respiration, alimentation, and excretory functions are provided by the placenta. Fetal tissue metabolism is oriented largely to anabolism; body temperature is modulated by maternal metabolism, and fetal tissue thermogenesis is maintained at a basal level. Tissue and organ growth appear to be regulated by growth factors which probably function by autocrine or paracrine mechanisms during most of gestation (72, 146-148). In this milieu conventional endocrine control systems are largely redundant, and other transient systems more appropriate to the intrauterine environment have evolved. We have developed some insights into these systems, but much more information is necessary before we can truly understand this fascinating environment.
Assuntos
Glândulas Endócrinas/embriologia , Feto/fisiologia , Glândulas Suprarrenais/embriologia , Glândulas Suprarrenais/fisiologia , Água Corporal/metabolismo , Calcitonina/fisiologia , Cálcio/fisiologia , Desenvolvimento Embrionário e Fetal , Glândulas Endócrinas/fisiologia , Estrogênios/biossíntese , Feminino , Humanos , Hidrocortisona/fisiologia , Hormônios Hipotalâmicos/fisiologia , Trabalho de Parto , Masculino , Hormônio Paratireóideo/fisiologia , Hipófise/embriologia , Hipófise/fisiologia , Neuro-Hipófise/embriologia , Neuro-Hipófise/fisiologia , Hormônios Hipofisários/fisiologia , Gravidez , Receptores de Superfície Celular/fisiologia , Diferenciação Sexual , Estresse Fisiológico/embriologia , Estresse Fisiológico/fisiopatologia , Testículo/embriologia , Testículo/fisiologia , Hormônios Tireóideos/fisiologiaRESUMO
Diapause-destined embryos of the crustacean Artemia franciscana arrest as gastrulae, acquire extreme stress tolerance, and enter profound metabolic dormancy. Among genes upregulated at 2 days postfertilization in these embryos is a homologue of p8, a stress-inducible transcription cofactor. Artemia p8 is smaller than vertebrate homologues but shares a basic helix-loop-helix domain and a bipartite nuclear localization signal. Probing of restriction digested DNA on Southern blots indicated a single Artemia p8 gene and 5'-RACE specified 2 transcription start sites. Several putative cis-acting regulatory sequences, including two heat shock elements, appeared upstream of the p8 transcription start site. Artemia p8 mRNA increased sharply at 1 day postfertilization in diapause-destined embryos and then declined, whereas p8 protein appeared 2 days postfertilization and remained relatively constant throughout development, indicating a stable protein. p8 was not detectable in nauplius-destined (nondiapause) Artemia embryos. Immunofluorescent staining revealed p8 within Artemia nuclei. The results support the idea that p8, a known stressresponsive transcription cofactor, mediates gene expression in diapause-destined Artemia embryos. p8 is the first diapause-related transcription factor identified in crustaceans and 1 of only a small number of such proteins identified in any organism undergoing diapause.
Assuntos
Artemia/metabolismo , Fatores de Transcrição Hélice-Alça-Hélice Básicos/metabolismo , Embrião não Mamífero/metabolismo , Estresse Fisiológico/metabolismo , Adaptação Fisiológica/genética , Sequência de Aminoácidos , Animais , Artemia/embriologia , Artemia/crescimento & desenvolvimento , Sequência de Bases , Fatores de Transcrição Hélice-Alça-Hélice Básicos/química , Fatores de Transcrição Hélice-Alça-Hélice Básicos/genética , Regulação da Expressão Gênica no Desenvolvimento , Humanos , Dados de Sequência Molecular , Proteínas de Neoplasias/química , Conformação Proteica , Estrutura Terciária de Proteína , RNA Mensageiro/metabolismo , Homologia de Sequência de Aminoácidos , Estresse Fisiológico/embriologia , Estresse Fisiológico/genética , Estresse Fisiológico/fisiopatologia , Fatores de TempoRESUMO
Neurodevelopmental changes induced by environmental stress exposure play a significant but poorly defined role in the etiology of schizophrenia. Exposure of pregnant female rats to a series of unpredictable stresses during the final week of pregnancy generates behavioral deficits and molecular changes in the offspring similar to those observed in schizophrenic individuals. We used this rat prenatal stress preparation to investigate social withdrawal behaviors that may have relevance to the negative symptoms of schizophrenia. The cumulative time adult male offspring of stress-exposed pregnant female rats actively interacted with a weight-matched, same-sex peer was decreased approximately 76% relative to non-stress exposed control rats. Prenatal stress exposure also diminished the quality of the social interaction behavior indicative of reduced social drive. Analysis of the oxytocinergic system in the prenatally stressed male rats revealed significantly less oxytocin mRNA in the paraventricular nucleus and increased oxytocin receptor binding in the central amygdala. Moreover, oxytocin, but not vasopressin, administration into the central amygdala reversed the social incompetence of the prenatally stressed rats without increasing behavior in non-stressed control animals. In addition, cross-fostering pups from prenatally stressed mothers to non-stressed mothers failed to improve the social deficit of the prenatally stressed male offspring. Two behavioral assays designed to measure anxiety did not differentiate the prenatally stressed rats from non-stressed controls. These data indicate that prenatal stress may be an etiologically appropriate animal model for some aspects of schizophrenic social withdrawal. Furthermore, unpredictable prenatal stress exposure selectively degrades social interaction behaviors without increasing anxiety measures.
Assuntos
Ocitocina/farmacologia , Comportamento Social , Estresse Fisiológico/embriologia , Tonsila do Cerebelo/efeitos dos fármacos , Tonsila do Cerebelo/embriologia , Tonsila do Cerebelo/fisiologia , Animais , Modelos Animais de Doenças , Feminino , Humanos , Hipotálamo/efeitos dos fármacos , Hipotálamo/embriologia , Hipotálamo/fisiologia , Gravidez , Complicações na Gravidez/psicologia , Efeitos Tardios da Exposição Pré-Natal , Ratos , Psicologia do Esquizofrênico , Estresse Fisiológico/prevenção & controle , Estresse Fisiológico/psicologiaRESUMO
The molecular and cellular mechanisms by which plasticity is induced in the mature CNS (and, specifically, in the hippocampus) by environmental input are progressively being elucidated. However, the mechanisms - and even the existence - of functional and structural effects of environmental input (and, particularly, stress) early in life are incompletely understood. Here, we discuss recent evidence that stressful stimuli have a significant impact on neonatal (rat) and prenatal (human) hippocampal function and integrity. Stressful signals provoke expression and release of neuromodulators, including the peptide corticotropin-releasing hormone (CRH), leading to activation of CRH receptors on principal hippocampal neurons. Although physiological activation of these receptors promotes synaptic efficacy, pathological levels of CRH at hippocampal synapses contribute to neuronal death. Thus, early-life stress could constitute a 'double-edged sword': mild stress might promote hippocampal-dependent cognitive function, whereas severe stress might impair neuronal function and survival, both immediately and in the long-term. Importantly, these CRH-mediated processes could be targets of preventive and interventional strategies.
Assuntos
Estresse Fisiológico/embriologia , Estresse Fisiológico/fisiopatologia , Envelhecimento/fisiologia , Animais , Encéfalo/fisiopatologia , Hormônio Liberador da Corticotropina/metabolismo , Feto/fisiologia , Humanos , Sistema Límbico/fisiopatologia , Vias Neurais/fisiopatologia , Neurônios/fisiologiaRESUMO
There is now widespread agreement that small size at birth is associated with an increased risk of the metabolic syndrome (glucose intolerance, high blood pressure, and dyslipidemia) and related pathologies, including cardiovascular disease in later life. Evidence is emerging that suggests that programming of hormonal systems in response to an adverse fetal environment may be one of the mechanisms underlying these long-term consequences of growth restriction in early life. In particular, alterations in neuroendocrine responses to stress may be important. Recent research suggests that increased adrenocortical and sympathoadrenal responses are associated with small size at birth. Epidemiological studies show that such physiological alterations in these neuroendocrine systems may have potent effects on risk of cardiovascular disease through their influence on risk factors, such as plasma glucose and lipid concentrations and blood pressure.
Assuntos
Recém-Nascido de Baixo Peso/fisiologia , Síndrome Metabólica/embriologia , Estresse Fisiológico/embriologia , Sistema Nervoso Autônomo/fisiologia , Humanos , Recém-Nascido , Neuroendocrinologia , Fatores de RiscoRESUMO
During the past decade, a considerable body of evidence has emerged showing that circumstances during the fetal period may have lifelong programming effects on different body functions with a considerable impact on disease susceptibility. The purpose of this article is to provide a synopsis of these findings and their role in explaining the development of stress-related adult disease. In the context of Per Björntorp memorial symposium, stress-related disease will be interpreted broadly, including cardiovascular disease and components of the metabolic syndrome, for which the evidence of fetal origins is most abundant. It has however become evident that early-life programming has a much broader potential effect on an individual's health. For example, perinatal variables, such as low birth weight, have been associated with increased prevalence of depressive symptoms. Mechanistic studies in animals and humans have shown that lifelong programming of the hypothalamic-pituitary-adrenal axis (HPAA) function by fetal life conditions is likely to be a key factor in mediating associations with these disorders, which frequently are characterized by HPAA overactivity. Preliminary observations suggest a similar important role for early-life programming of sympathoadrenal function. Reduced HPAA activity is characteristic of a number of stress-related disorders, including posttraumatic stress disorder; chronic pain; fatigue; and atypical, melancholic depression. It is therefore highly plausible that susceptibility to these disorders originates in a similar manner during early life, although direct evidence is to a great deal lacking. Important targets for future research include distinction between the effects of different pregnancy conditions, such as maternal malnutrition, preeclampsia, and maternal infection, which may have dissimilar late-life consequences. This will be a crucial step when the associations that are currently emerging will be translated into disease prevention.
Assuntos
Suscetibilidade a Doenças/embriologia , Desenvolvimento Fetal/fisiologia , Estresse Fisiológico/embriologia , Sistema Nervoso Autônomo/fisiologia , Peso ao Nascer/fisiologia , Feminino , Humanos , Sistema Hipotálamo-Hipofisário/fisiologia , Sistema Hipófise-Suprarrenal/fisiologia , Gravidez , Transtornos de Estresse Pós-Traumáticos/metabolismo , Estresse Psicológico/metabolismoRESUMO
Extreme environments are closely associated with phenotypic evolution, yet the mechanisms behind this relationship are poorly understood. Several themes and approaches in recent studies significantly further our understanding of the importance that stress-induced variation plays in evolution. First, stressful environments modify (and often reduce) the integration of neuroendocrinological, morphological and behavioural regulatory systems. Second, such reduced integration and subsequent accommodation of stress-induced variation by developmental systems enables organismal 'memory' of a stressful event as well as phenotypic and genetic assimilation of the response to a stressor. Third, in complex functional systems, a stress-induced increase in phenotypic and genetic variance is often directional, channelled by existing ontogenetic pathways. This accounts for similarity among individuals in stress-induced changes and thus significantly facilitates the rate of adaptive evolution. Fourth, accumulation of phenotypically neutral genetic variation might be a common property of locally adapted and complex organismal systems, and extreme environments facilitate the phenotypic expression of this variance. Finally, stress-induced effects and stress-resistance strategies often persist for several generations through maternal, ecological and cultural inheritance. These transgenerational effects, along with both the complexity of developmental systems and stressor recurrence, might facilitate genetic assimilation of stress-induced effects. Accumulation of phenotypically neutral genetic variance by developmental systems and phenotypic accommodation of stress-induced effects, together with the inheritance of stress-induced modifications, ensure the evolutionary persistence of stress-response strategies and provide a link between individual adaptability and evolutionary adaptation.
Assuntos
Aclimatação/genética , Adaptação Fisiológica/genética , Comportamento Animal/fisiologia , Evolução Biológica , Meio Ambiente , Variação Genética , Fenótipo , Estresse Fisiológico/genética , Animais , Estresse Fisiológico/embriologia , Estresse Fisiológico/fisiopatologiaRESUMO
We have shown that prenatal restraint stress (PNRS) induces higher levels of anxiety, greater vulnerability to drugs, a phase advance in the circadian rhythm of locomotor activity and an increase in the paradoxical sleep in adult rats. These behavioral effects result from permanent modifications to the functioning of the brain, particularly in the feedback mechanisms of the hypothalamic-pituitary-adrenal (HPA) axis: the secretion of corticosterone is prolonged after stress and the number of the central glucocorticoid receptors is reduced. These abnormalities are associated with modifications in the synthesis and/or release of certain neurotransmitters. Dysfunction of the HPA axis is due, in part, to stress-induced maternal increase of glucocorticoids, which influences fetal brain development. Some biological abnormalities in depression can be related to those found in PNRS rats reinforcing the idea of the usefulness of PNRS rats as an appropriate animal model to study new pharmacological approaches.
Assuntos
Glucocorticoides/sangue , Estresse Fisiológico/embriologia , Animais , Transtornos de Ansiedade/fisiopatologia , Comportamento Animal/fisiologia , Depressão , Feminino , Previsões , Glucocorticoides/fisiologia , Humanos , Comportamento Materno/fisiologia , Modelos Animais , Periodicidade , Gravidez , Estresse Fisiológico/fisiopatologiaRESUMO
Studies in rodents and nonhuman primates indicate that maternal stress during pregnancy can influence the developing fetus, resulting in delay of motor and cognitive development and impaired adaptation to stressful situations. These effects may be mediated by the hypothalamic-pituitary-adrenal (HPA) axis. We examined whether stress during pregnancy predicted developmental outcome of human infants in a prospective design. Self-report data about daily hassles and pregnancy-specific anxiety and salivary cortisol levels were collected in nulliparous pregnant women. Dependent measures were scores on the Bayley Scales of Infant Development and on temperamental questionnaires at 3 and 8 months. Pregnancy-specific anxiety in mid pregnancy predicted lower mental and motor developmental scores at 8 months. Early morning values of cortisol in late pregnancy were negatively related to both mental and motor development at 3 months and motor development at 8 months. Pregnancy-specific anxiety explained 7% of the variance of test-affectivity and goal-directedness at 8 months. Increased maternal stress during pregnancy seems to be one of the determinants of temperamental variation and delay of development of infants and may be a risk factor for developing psychopathology later in life.
Assuntos
Cognição/fisiologia , Comportamento do Lactente/fisiologia , Efeitos Tardios da Exposição Pré-Natal , Estresse Fisiológico/embriologia , Temperamento/fisiologia , Animais , Feminino , Humanos , Lactente , Comportamento do Lactente/psicologia , Gravidez , Estresse Fisiológico/psicologiaRESUMO
Phenotypic plasticity of wing size and shape of Drosophila simulans was analyzed across the entire range of viable developmental temperatures with Procrustes geometric morphometric method. In agreement with previous studies, size clearly decreases when temperature increases. Wing shape variation was decomposed into its allometric (24%) and nonallometric (76%) components, and both were shown to involve landmarks located throughout the entire wing blade. The allometric component basically revealed a progressive, monotonous variation along the temperature. Surprisingly, nonallometric shape changes were highly similar at both extremes of the thermal range, suggesting that stress, rather than temperature per se, is the key developmental factor affecting wing shape.
Assuntos
Drosophila/embriologia , Estresse Fisiológico/embriologia , Temperatura , Asas de Animais/anatomia & histologia , Análise de Variância , Animais , Biometria , Pesos e Medidas Corporais , Drosophila/anatomia & histologia , Asas de Animais/embriologiaRESUMO
Prenatal exposure to alcohol alters postnatal function of the hypothalamic-pituitary-adrenal axis. Hyperresponsiveness to stress, or increased secretion of corticosterone, is a commonly studied effect in offspring of rats exposed to alcohol during a substantial period of gestation. No studies have reported on stress hormone secretion following alcohol exposure on a single day during embryonic development even though exposure at this time may damage the hypothalamus and pituitary. To explore the effect of an acute exposure, we used the offspring of C57BL/6J mice exposed to alcohol or saline on embryonic day (E) 9 (2.9 g/kg administered twice, 4h apart). At 7.5 or 22 months of age these mice were subjected to a 12-h restraint stress, or merely kept in the same environment without restraint. After the 12-h period, a blood sample was obtained from the retro-orbital plexus, and analyzed for the amount of corticosterone. The 7.5-month old group of alcohol-treated offspring were indeed hyperresponsive to restraint stress, but the 22-month old mice were not. Whether the normal-appearing corticosterone response of the old alcohol-exposed mice indicated adaptation to restraint, an aging-associated ceiling effect in corticosterone secretion, or an expression of pathology, cannot be decided on the basis of present data.
Assuntos
Envelhecimento/sangue , Envelhecimento/efeitos dos fármacos , Corticosterona/sangue , Etanol/toxicidade , Efeitos Tardios da Exposição Pré-Natal , Estresse Fisiológico/sangue , Estresse Fisiológico/embriologia , Envelhecimento/fisiologia , Animais , Feminino , Camundongos , Camundongos Endogâmicos C57BL , Gravidez , Restrição Física , Estresse Fisiológico/fisiopatologia , Fatores de TempoRESUMO
Subcutaneous injections of alkaline saline were made perinatally in Sprague-Dawley rats according to two schedules. In a pre-/postnatal group, dams were treated from 19th gestational day to 9th day postpartum and pups from day 0-9. In a postnatal group, pups alone were injected from day 0-6. At 19-23, 50-56 and 82-86 days of age, injected rats and uninjected controls were anesthetized and arterial blood pressure measured. Rats from the pre-/postnatal group had higher blood pressures (58%) and body weights at 19-23 days and lower blood pressure (35%) and body weight at 82-86 days of age. Blood pressure and body weight were comparable to control at all ages in the postnatal injection group. It is concluded that as a result of the maternal stress produced by the injections there was a generalized disturbance of growth processes resulting in hypotension and decreased body weight in adulthood.
Assuntos
Envelhecimento , Pressão Sanguínea , Feto/fisiologia , Crescimento , Complicações na Gravidez/fisiopatologia , Estresse Fisiológico/fisiopatologia , Animais , Peso Corporal , Feminino , Injeções Subcutâneas , Gravidez , Ratos , Ratos Endogâmicos , Cloreto de Sódio/administração & dosagem , Estresse Fisiológico/embriologiaRESUMO
Field studies reveal that bank vole females' mobility and aggression increase during pregnancy. Here we investigated the reaction of pregnant females to social stress evoked by short but frequent meetings with another female at the same stage of pregnancy. The stress neither evoked pregnancy termination nor affected pregnancy duration but had a long-term effect on the reproductive activity of the offspring. Prenatal stress reduced the rate of sexual maturation of voles as estimated at the age of 20 days. Uterine weights of prenatally stressed females and testes weights of prenatally stressed males were significantly lower than in offspring born to nonstressed mothers. Olfactory signals are known to be important in the sexual preferences of bank voles. Adult prenatally stressed females were more attractive to other adult females than were nonstressed animals. For bank vole males, however, prenatal stress decreased the attractiveness of females; adult males selected nonstressed females over stressed partners, by odor. This study shows that prenatal conditions evoked by short but frequent encounters with another pregnant female lead to delayed puberty in females and males, and decrease sexual attractiveness in adult offspring. These two negative effects may significantly limit the reproduction of prenatally stressed offspring.
Assuntos
Envelhecimento , Arvicolinae/embriologia , Arvicolinae/fisiologia , Efeitos Tardios da Exposição Pré-Natal , Comportamento Sexual Animal , Maturidade Sexual , Estresse Fisiológico/embriologia , Animais , Arvicolinae/crescimento & desenvolvimento , Arvicolinae/psicologia , Feminino , Relações Interpessoais , Masculino , Odorantes , Gravidez , Olfato , Estresse Fisiológico/etiologiaRESUMO
We tested the hypothesis that prenatal stress would enhance conditioned fear in adult rats. Pregnant Sprague-Dawley rats were stressed by exposure to a novel environment and subcutaneous injection of saline (0.1 ml 0.9% NaCl) at random times daily from Days 14 to 21 of pregnancy. When compared to adult control (CON) male rats from unmanipulated pregnancies, adult prenatally stressed (PS) male rats showed increased freezing behavior in response to acute footshock as well as increased freezing behavior the next day in the same context, without shock delivery. In another experiment, the gestational stressor was examined for elevations in corticosterone and ACTH. At gestational days (G)15, G17, G19 and G21, maternal and fetal plasma was collected. Analysis showed elevations in corticosterone and ACTH in the PS dams when compared to the CON dams. Additionally, increased corticosterone was found in the PS fetuses when compared to the CON fetuses. Finally, some CON and PS litters were examined for alterations in length of gestation, number of pups born, bodyweight on postnatal day (P)1 and anogenital distance on P1 and differences were not found. In conclusion, our data demonstrate that a mild stressor during gestation, sufficient to raise plasma corticosterone and ACTH, is associated with enhanced conditioned fear during adulthood.
Assuntos
Envelhecimento/psicologia , Condicionamento Psicológico , Medo/psicologia , Efeitos Tardios da Exposição Pré-Natal , Estresse Fisiológico/embriologia , Estresse Fisiológico/psicologia , Hormônio Adrenocorticotrópico/sangue , Animais , Animais Recém-Nascidos/crescimento & desenvolvimento , Corticosterona/sangue , Feminino , Sangue Fetal , Masculino , Gravidez , Complicações na Gravidez/sangue , Ratos , Ratos Sprague-Dawley , Estresse Fisiológico/sangueRESUMO
The aim of the present study was to investigate the effects of postnatal oxytocin (OT) treatment and postnatal stroking on blood pressure and heart rate in adult rats. For this purpose, rats were treated subcutaneously with OT (1 mg/kg) once a day on days 1-14 after birth, or exposed to stroking on the ventral side of the abdomen for 5 min once a day on days 1-7 after birth. Blood pressure and heart rate were measured at the age of 7-8 months. The OT-treated male rats had a significantly reduced diastolic blood pressure in adulthood (p < 0.001), and in the female rats, both systolic (p < 0.01) and diastolic blood pressures (p < 0.001) were significantly lower compared to controls given saline postnatally. OT reduced blood pressure also in prenatally stressed female rats, which had a significantly higher blood pressure in adulthood compared to control rats that had not been exposed to prenatal stress. Also, the postnatal stroking reduced diastolic blood pressure in adulthood (p < 0.05). No changes in heart rate were found. In conclusion, both postnatal OT treatment and postnatal stroking reduced blood pressure in adulthood. In addition, in female rats, OT reduced the increase in blood pressure caused by prenatal stress.
Assuntos
Envelhecimento/fisiologia , Animais Recém-Nascidos/fisiologia , Pressão Sanguínea/efeitos dos fármacos , Pressão Sanguínea/fisiologia , Manobra Psicológica , Ocitocina/farmacologia , Animais , Animais Recém-Nascidos/crescimento & desenvolvimento , Diástole , Feminino , Feto/fisiologia , Frequência Cardíaca/efeitos dos fármacos , Frequência Cardíaca/fisiologia , Masculino , Gravidez , Efeitos Tardios da Exposição Pré-Natal , Ratos , Ratos Sprague-Dawley , Caracteres Sexuais , Estresse Fisiológico/embriologia , SístoleRESUMO
The concentration of corticosterone in the suprarenals after the stress effect (injection of formol) was studied in 20.5 days old foetuses of the adrenalectomized rats, using the method of competitive binding. The concentration of corticosterone in the suprarenals of normal foetuses increased reliably within 30 min after the injection of formol; this reaction was absent in the encephalectomized foetuses. The results obtained suggest the participation of embryonic hypothalamus in the organization of stress response during prenatal development of rats.