RESUMO
Previous work has identified the adolescent period as particularly sensitive to the short- and long-term effects of marijuana and its main psychoactive component Δ9-tetrahydrocannabinol (THC). However, other studies have identified certain backgrounds as more sensitive than others, including the sex of the individual or the strain of the rat used. Further, the effects of THC may be specific to certain behavioural tasks (e.g. measures of anxiety), and the consequences of THC are not seen equally across all behavioural measures. Here, data obtained from adolescent male and female Long-Evans and Wistar rats exposed to THC and tested as adults, which, using standard ANOVA testing, showed strain- and sex-specific effects of THC, was analyzed using principal component analysis (PCA). PCA allowed for the examination of the relative contribution of our variables of interest to the variance in the data obtained from multiple behavioural tasks, including the skilled reaching task, the Morris water task, the discriminative fear-conditioning to context task, the elevated plus maze task and the conditioned place preference task to a low dose of amphetamine, as well as volumetric estimates of brain volumes and cfos activation. We observed that early life experience accounted for a large proportion of variance across data sets, although its relative contribution varied across tasks. Additionally, THC accounted for a very small proportion of the variance across all behavioural tasks. We demonstrate here that by using PCA, we were able to describe the main variables of interest and demonstrate that THC exposure had a negligible effect on the variance in the data set.
Assuntos
Encéfalo/efeitos dos fármacos , Dronabinol/farmacologia , Psicotrópicos/farmacologia , Ratos Long-Evans/fisiologia , Ratos Wistar/fisiologia , Caracteres Sexuais , Envelhecimento , Animais , Ansiedade/fisiopatologia , Encéfalo/anatomia & histologia , Encéfalo/crescimento & desenvolvimento , Encéfalo/fisiologia , Feminino , Aprendizagem/efeitos dos fármacos , Aprendizagem/fisiologia , Masculino , Memória/efeitos dos fármacos , Memória/fisiologia , Destreza Motora/efeitos dos fármacos , Destreza Motora/fisiologia , Tamanho do Órgão , Análise de Componente Principal , Testes Psicológicos , Ratos Long-Evans/anatomia & histologia , Ratos Long-Evans/psicologia , Ratos Wistar/anatomia & histologia , Ratos Wistar/psicologia , Especificidade da EspécieRESUMO
Marijuana is one of the most highly used psychoactive substances in the world, and its use typically begins during adolescence, a period of substantial brain development. Females across species appear to be more susceptible to the long-term consequences of marijuana use. Despite the identification of inherent differences between rat strains including measures of anatomy, genetics and behaviour, no studies to our knowledge have examined the long-term consequences of adolescent exposure to marijuana or its main psychoactive component, Δ(9)-tetrahydrocannabinol (THC), in males and females of two widely used rat strains: Long-Evans hooded (LER) and Wistar (WR) rats. THC was administered for 14 consecutive days following puberty onset, and once they reached adulthood, changes in behaviour and in the volume of associated brain areas were quantified. Rats were assessed in behavioural tests of motor, spatial and contextual learning, and anxiety. Some tasks showed effects of injection, since handled and vehicle groups were included as controls. Performance on all tasks, except motor learning, and the volume of associated brain areas were altered with injection or THC administration, although these effects varied by strain and sex group. Finally, analysis revealed treatment-specific correlations between performance and brain volumes. This study is the first of its kind to directly compare males and females of two rat strains for the long-term consequences of adolescent THC exposure. It highlights the importance of considering strain and identifies certain rat strains as susceptible or resilient to the effects of THC.
Assuntos
Encéfalo/efeitos dos fármacos , Dronabinol/farmacologia , Psicotrópicos/farmacologia , Ratos Long-Evans/fisiologia , Ratos Wistar/fisiologia , Caracteres Sexuais , Envelhecimento , Animais , Ansiedade/fisiopatologia , Encéfalo/anatomia & histologia , Encéfalo/crescimento & desenvolvimento , Encéfalo/fisiologia , Feminino , Aprendizagem/efeitos dos fármacos , Aprendizagem/fisiologia , Masculino , Memória/efeitos dos fármacos , Memória/fisiologia , Destreza Motora/efeitos dos fármacos , Destreza Motora/fisiologia , Tamanho do Órgão , Testes Psicológicos , Ratos Long-Evans/anatomia & histologia , Ratos Long-Evans/psicologia , Ratos Wistar/anatomia & histologia , Ratos Wistar/psicologia , Especificidade da EspécieRESUMO
Alterations in behaviour can arise through a number of factors, including strain and sex. Here, we explored strain and sex differences between Long-Evans (LER) and Wistar (WR) male and female rats that had been trained in a myriad of behavioural tasks. Tests included those assessing motor learning (skilled reaching task), spatial learning and memory (Morris water task), contextual learning (discriminative fear-conditioning to context) and anxiety behaviour (elevated plus maze). Following behavioural assessment, associated brain areas were examined for volumetric differences, including the hippocampus and its subregions, prefrontal cortex areas and the amygdala. LER and WR differed in their rates of performance in the skilled reaching task throughout the training period. Overall, LER outperformed WR in tasks related to contextual and spatial learning, although this was not accompanied by larger volumes of associated brain areas. Males outperformed females in spatial learning, and females outperformed males in the contextual fear-conditioning task and had an associated larger amygdalar volume, although these sexual dimorphisms were only observed within the LER strain. Overall, this study highlights differences between these two rat strains as well as highlights that larger volumetric estimates of brain areas do not always confer improved function of associated behaviours.
Assuntos
Ratos Long-Evans/fisiologia , Ratos Long-Evans/psicologia , Ratos Wistar/fisiologia , Ratos Wistar/psicologia , Caracteres Sexuais , Animais , Ansiedade/fisiopatologia , Encéfalo/anatomia & histologia , Encéfalo/fisiologia , Feminino , Aprendizagem/fisiologia , Masculino , Memória/fisiologia , Destreza Motora/fisiologia , Tamanho do Órgão , Testes Psicológicos , Ratos Long-Evans/anatomia & histologia , Ratos Wistar/anatomia & histologia , Especificidade da EspécieRESUMO
Intracortical microstimulation of the frontal cortex evokes movements in the contralateral limbs, paws, and digits of placental mammals including the laboratory rat. The topographic representation of movement in the rat consists of a rostral forelimb area (RFA), a caudal forelimb area (CFA), and a hind limb area (HLA). The size of these representations can vary between individual animals and the proportional representation of the body parts within regions can also change as a function of experience. To date, there have been no investigations of strain differences in the cortical map of rats, and this was the objective of the present investigation. The effect of cortical stimulation was compared in young male Long-Evans rats and Fischer-344 rats. The overall size of the motor cortex representation was greater in Long-Evans rats compared to Fischer-344 rats and the threshold required to elicit a movement was higher in the Fischer-344 rats. An additional set of animals were trained in a skilled reaching task to rule out the possibility that experiential differences in the groups could account for the result and to examine the relationship between the differences in topography of cortical movement representations and motor performance. The Long-Evans rats were quantitatively and qualitatively better in skilled reaching than the Fischer-344 rats. Also, Long-Evans rats exhibited a relatively larger area of the topographic representation and lower thresholds for eliciting movement in the contralateral forelimb. This is the first study to describe pronounced strain-related differences in the microstimulation-topographic map of the motor cortex. The results are discussed in relation to using strain differences as a way of examining the behavioral, the physiological, and the anatomical organization of the motor system.
Assuntos
Mapeamento Encefálico , Córtex Motor/fisiologia , Destreza Motora/fisiologia , Ratos Endogâmicos F344/fisiologia , Ratos Long-Evans/fisiologia , Animais , Estimulação Elétrica , Membro Anterior/inervação , Membro Posterior/inervação , Masculino , Córtex Motor/anatomia & histologia , Movimento/fisiologia , Ratos , Ratos Endogâmicos F344/anatomia & histologia , Ratos Long-Evans/anatomia & histologia , Especificidade da EspécieRESUMO
Distinctive subsets of glutamatergic neurons in cerebral cortex sequester the transition metal zinc within the synaptic vesicles of their axon terminals. In the present study we used histochemical localization of synaptic zinc to investigate normal postnatal development and experience-dependent plasticity of zinc-containing circuits in somatosensory barrel cortex of rats. First, we found that zinc-containing cortical circuits are dynamically reorganized between postnatal day (P) 0 and P28. Whereas most cortical laminae exhibited idiosyncratic increases in zinc histochemical staining with advancing age, lamina IV barrels were darkly reactive early in life and then lost much of their complement of synaptic zinc during postnatal weeks 2-4. Second, we established that sensory experience plays a major role in sculpting the zinc-containing innervation of cortical barrels. Trimming a particular facial whisker arrested the normal postnatal decline in synaptic zinc in the corresponding, deprived barrel. This resulted in more intense zinc staining in deprived barrels compared with adjacent, nondeprived barrels. Notably, the influence of experience on development of zinc circuits was most robust during a critical period extending from about P14, when an effect of whisker trimming first could be observed, through P28, after which time chronic deprivation no longer resulted in heightened levels of synaptic zinc in lamina IV. These findings indicate that sensory input can have a marked influence on development of cortical circuits, including those within lamina IV, throughout the first postnatal month.
Assuntos
Vias Aferentes/crescimento & desenvolvimento , Vias Neurais/crescimento & desenvolvimento , Plasticidade Neuronal/fisiologia , Terminações Pré-Sinápticas/metabolismo , Ratos Long-Evans/crescimento & desenvolvimento , Córtex Somatossensorial/crescimento & desenvolvimento , Vibrissas/crescimento & desenvolvimento , Zinco/metabolismo , Vias Aferentes/citologia , Vias Aferentes/metabolismo , Envelhecimento/metabolismo , Animais , Animais Recém-Nascidos , Diferenciação Celular/fisiologia , Feminino , Masculino , Vias Neurais/citologia , Vias Neurais/metabolismo , Gravidez , Terminações Pré-Sinápticas/ultraestrutura , Ratos , Ratos Long-Evans/anatomia & histologia , Ratos Long-Evans/metabolismo , Privação Sensorial/fisiologia , Córtex Somatossensorial/citologia , Córtex Somatossensorial/metabolismo , Tato/fisiologia , Vibrissas/citologia , Vibrissas/metabolismoRESUMO
In cerebral cortex of rat and monkey, the neuropeptide somatostatin (SOM) marks a population of nonpyramidal cells (McDonald et al. [1982] J. Neurocytol. 11:809-824; Hendry et al. [1984] J. Neurosci. 4:2497:2517; Laemle and Feldman [1985] J. Comp. Neurol. 233:452-462; Meineke and Peters [1986] J. Neurocytol. 15:121-136; DeLima and Morrison [1989] J. Comp. Neurol. 283:212-227) that represent a distinct type of gamma-aminobutyric acid (GABA) -ergic neuron (Gonchar and Burkhalter [1997] Cereb. Cortex 7:347-358; Kawaguchi and Kubota [1997] Cereb. Cortex 7:476-486) whose synaptic connections are incompletely understood. The organization of inhibitory inputs to the axon initial segment are of particular interest because of their role in the suppression of action potentials (Miles et al. [1996] Neuron 16:815:823). Synapses on axon initial segments are morphologically heterogeneous (Peters and Harriman [1990] J. Neurocytol. 19:154-174), and some terminals lack parvalbumin (PV) and contain calbindin (Del Rio and DeFelipe [1997] J. Comp. Neurol. 342:389-408), that is also expressed by many SOM-immunoreactive neurons (Kubota et al. [1994] Brain Res. 649:159-173; Gonchar and Burkhalter [1997] Cereb. Cortex 7:347-358). We studied the innervation of pyramidal neurons by SOM neurons in rat and monkey visual cortex and examined putative contacts by confocal microscopy and determined synaptic connections in the electron microscope. Through the confocal microscope, SOM-positive boutons were observed to form close appositions with somata, dendrites, and spines of intracortically projecting pyramidal neurons of rat area 17 and pyramidal cells in monkey striate cortex. In addition, in rat and monkey, SOM boutons were found to be associated with axon initial segments of pyramidal neurons. SOM axon terminals that were apposed to axon initial segments of pyramidal neurons lacked PV, which was shown previously to label axo-axonic terminals provided by chandelier cells (DeFelipe et al. [1989] Proc. Natl. Acad. Sci. USA 86:2093-2097; Gonchar and Burkhalter [1999a] J. Comp. Neurol. 406:346:360). Electron microscopic examination directly demonstrated that SOM axon terminals form symmetric synapses with the initial segments of pyramidal cells in supragranular layers of rat and monkey primary visual cortex. These SOM synapses differed ultrastructurally from the more numerous unlabeled symmetric synapses found on initial segments. Postembedding immunostaining revealed that all SOM axon terminals contained GABA. Unlike PV-expressing chandelier cell axons that innervate exclusively initial segments of pyramidal cell axons, SOM-immunoreactive neurons innervate somata, dendrites, spines, and initial segments, that are just one of their targets. Thus, SOM neurons may influence synaptic excitation of pyramidal neurons at the level of synaptic inputs to dendrites as well as at the initiation site of action potential output.
Assuntos
Macaca fascicularis/anatomia & histologia , Terminações Pré-Sinápticas/ultraestrutura , Células Piramidais/ultraestrutura , Ratos Long-Evans/anatomia & histologia , Somatostatina/metabolismo , Córtex Visual/ultraestrutura , Ácido gama-Aminobutírico/metabolismo , Animais , Imuno-Histoquímica , Interneurônios/metabolismo , Interneurônios/ultraestrutura , Macaca fascicularis/metabolismo , Microscopia Confocal , Microscopia Eletrônica , Inibição Neural/fisiologia , Vias Neurais/metabolismo , Vias Neurais/ultraestrutura , Terminações Pré-Sinápticas/metabolismo , Células Piramidais/metabolismo , Ratos , Ratos Long-Evans/metabolismo , Transmissão Sináptica/fisiologia , Córtex Visual/metabolismoRESUMO
In a previous study, we found that the forepaw representation in the primary somatosensory cortex of rats housed in standard laboratory conditions was drastically altered during the aging process. In other studies we reported that exposure to an enriched environment improved the topographical organization and increased the spatial resolution of the forepaw cutaneous map in young adult rats, whereas housing in impoverished environment resulted in a loss of somatotopic details in the forepaw map. The main purpose of the present study was to investigate the influence of differential sensorimotor experience promoted by exposure to enriched or impoverished environments on the mutability of the cortical forepaw representation during aging. Two groups of Long-Evans rats were reared in enriched and impoverished environments from weaning to the age of 3.5-5 months (young adults), 6.5-8 months (mature rats), and 23-28 months (senescent rats). The electrophysiological maps of the forepaw representation were based on the somatosensory 'submodality' (cutaneous vs. non-cutaneous), size, and location of the receptive fields of small clusters of layer IV neurons. Moreover, the mechanical thresholds of neuronal response to cutaneous stimulation were assessed with calibrated von Frey filaments in mature and senescent animals. Age-related alterations of the topographic features of the forepaw map were characterized by a decrease in and a fragmentation of the cortical zones serving the glabrous skin of the forepaw. These changes were less pronounced in the enriched rats than in the impoverished rats. Glabrous skin receptive fields were smaller in young adult and mature enriched rats than in their impoverished counterparts. However, during aging glabrous receptive fields increased in the enriched rats, but decreased in the senescent impoverished rats so that old rats of either groups displayed receptive fields of similar sizes; in contrast, the size of hairy skin receptive fields was not affected by housing conditions or aging. Measurement of the neuronal responses to calibrated forces applied to the skin indicated that cortical excitability to near-threshold cutaneous input was lower in senescent rats than in mature rats, regardless of environmental conditions. The present study demonstrates that use-dependent remodeling of somatosensory maps occurs throughout life and that environmental and social interactions can partially offset the age-related breakdown of somatosensory cortical maps.
Assuntos
Envelhecimento/fisiologia , Ambiente Controlado , Membro Anterior/fisiologia , Plasticidade Neuronal/fisiologia , Ratos Long-Evans/fisiologia , Privação Sensorial/fisiologia , Córtex Somatossensorial/fisiologia , Tato/fisiologia , Potenciais de Ação/fisiologia , Animais , Mapeamento Encefálico , Feminino , Membro Anterior/inervação , Mecanorreceptores/citologia , Mecanorreceptores/fisiologia , Estimulação Física , Ratos , Ratos Long-Evans/anatomia & histologia , Córtex Somatossensorial/anatomia & histologiaRESUMO
The transition metal zinc is an essential dietary constituent that is believed to serve an important intercellular signaling role at certain excitatory synapses in the central nervous system. In the present study, we used histochemical techniques to investigate the distribution of synaptic zinc during postnatal development of retinogeniculate projections in rats. From postnatal day (P) 1 until P-21, the pattern of zinc histochemical staining in the dorsal lateral geniculate nucleus (LGNd) precisely matched the distribution of axon terminals from the ipsilateral eye that were labeled by anterograde transport of horseradish peroxidase. Regions of the LGNd that contained only crossed axons were devoid of zinc staining. Abnormalities in the distribution of uncrossed retinogeniculate projections in albino versus pigmented rats were paralleled by identical variations in localization of synaptic zinc. Unilateral enucleation on P-10 was followed within 5 days by loss of zinc staining in the LGNd ipsilateral to the removed eye without affecting staining in the contralateral nucleus. Finally, the ability to detect zinc histochemically in the LGNd ceased at approximately P-24. These findings provide evidence that zinc is sequestered within synaptic boutons of a subpopulation of retinal ganglion cells whose axons terminate on the ipsilateral side of the brain. The duration of zinc staining overlaps with the major period of axonal remodeling in the LGNd, suggesting that synaptically released zinc may play a role in postnatal refinement of retinogeniculate projections.
Assuntos
Lateralidade Funcional/fisiologia , Corpos Geniculados/crescimento & desenvolvimento , Terminações Pré-Sinápticas/metabolismo , Retina/crescimento & desenvolvimento , Vias Visuais/crescimento & desenvolvimento , Zinco/metabolismo , Fatores Etários , Albinismo/metabolismo , Albinismo/patologia , Albinismo/fisiopatologia , Animais , Animais Recém-Nascidos , Padronização Corporal/fisiologia , Enucleação Ocular/efeitos adversos , Corpos Geniculados/citologia , Corpos Geniculados/metabolismo , Histocitoquímica/métodos , Plasticidade Neuronal/fisiologia , Terminações Pré-Sinápticas/ultraestrutura , Ratos , Ratos Long-Evans/anatomia & histologia , Ratos Long-Evans/crescimento & desenvolvimento , Ratos Long-Evans/metabolismo , Retina/citologia , Retina/metabolismo , Vias Visuais/citologia , Vias Visuais/metabolismoRESUMO
Although studies in the visual cortex have found gamma-aminobutyric acid B (GABA(B)) receptor-mediated pre- and postsynaptic inhibitory effects on neurons, the subcellular localization of GABA(B) receptors in different types of cortical neurons and synapses has not been shown directly. To provide this information, we have used antibodies against the GABA(B) receptor (R)1a/b and GABA(B)R2 subunits and have studied the localization of immunoreactivities in rat visual cortex. Light microscopic analyses have shown that both subunits are expressed in cell bodies and dendrites of 65-92% of corticocortically projecting pyramidal neurons and in 92-100% of parvalbumin (PV)-, calretinin (CR)-, and somatostatin (SOM)-containing GABAergic neurons. Electron microscopic analyses of immunoperoxidase- and immunogold-labeled tissue revealed staining in the nucleus, cytoplasm and cell surface membranes with both antibodies. Colocalization of both subunits was observed in all of these structures. GABA(B)R1a/b and GABA(B)R2 were concentrated in excitatory and inhibitory synapses and in extrasynaptic membranes. In GABAergic synapses, GABA(B)R1a/b and GABA(B)R2 were more strongly expressed postsynaptically on pyramidal and nonpyramidal cells than presynaptically. In type 1 synapses GABA(B)R1a/b and GABA(B)R2 was found in pre- and postsynaptic membranes. The nuclear localization of GABA(B)R1 and GABA(B)R2 subunits suggests a novel role for neurotransmitter receptors in controlling gene expression. The synaptic colocalization of GABA(B)R1 and GABA(B)R2 indicates that subunits form heteromeric assemblies of the functional receptor in inhibitory and excitatory synapses. Subunit coexpression in GABAergic synapses that include PV-containing and PV-deficient terminals suggests that pre- and postsynaptic GABA(B) receptor activation is provided by several different types of interneurons. The coexpression of both subunits in excitatory synapses suggests a role for GABA(B) receptors in the regulation of glutamate release and raises the question how these receptors are activated in the absence of pre-or postsynaptic GABAergic synaptic inputs to excitatory synapses.
Assuntos
Neurônios/metabolismo , Ratos Long-Evans/metabolismo , Receptores de GABA-B/metabolismo , Córtex Visual/metabolismo , Animais , Membrana Celular/metabolismo , Membrana Celular/ultraestrutura , Citoplasma/metabolismo , Citoplasma/ultraestrutura , Dendritos/metabolismo , Dendritos/ultraestrutura , Imuno-Histoquímica , Interneurônios/metabolismo , Interneurônios/ultraestrutura , Microscopia Eletrônica , Inibição Neural/fisiologia , Neurônios/ultraestrutura , Organelas/metabolismo , Organelas/ultraestrutura , Terminações Pré-Sinápticas/metabolismo , Terminações Pré-Sinápticas/ultraestrutura , Células Piramidais/metabolismo , Células Piramidais/ultraestrutura , Ratos , Ratos Long-Evans/anatomia & histologia , Receptores de GABA/metabolismo , Receptores de GABA-B/química , Córtex Visual/ultraestrutura , Ácido gama-Aminobutírico/metabolismoRESUMO
The morphology of olivocerebellar (OC) axons originating from the inferior olive (IO) was investigated in the rat by reconstructing the entire trajectories of single axons that had been labeled with biotinylated dextran amine. Virtually all of the OC axons entered the cerebellum through the inferior cerebellar peduncle (ICP) contralateral to the IO, with a few exceptions. Although most OC projection was contralateral, a few axons projected bilaterally by crossing the midline within the cerebellum. Collaterals of OC axons could be classified into thick branches and thin collaterals. Thick branches of each OC axon (6.1 +/- 3.7/OC axon, mean +/- SD for n = 16 axons) terminated as climbing fibers (CFs) on single Purkinje cells (PCs) in a one-to-one relationship. Besides terminal arborization around PC thick dendrites, CFs had terminals that surrounded a PC soma, fine branchlets that extended transversely in the molecular layer, and thin retrograde collaterals that re-entered the PC and granular layers. Innervation of a single PC by two CFs originating from the same axon was seen, although infrequently. Concerning thin collaterals, about half of the OC axons had one or only a few collaterals terminating in the white matter of the ICP, most had 1 to 6 collaterals terminating in a single cerebellar nucleus, and all had 3 to 16 collaterals that terminated mainly in the granular layer, but occasionally in the cerebellar white matter and the PC layer. Some swellings of thin collaterals touched somata of presumed Golgi cells and PCs. No OC axons terminated solely in the ICP, cerebellar nucleus or granular layer without giving rise to CFs.
Assuntos
Axônios , Núcleos Cerebelares/citologia , Bulbo/citologia , Núcleo Olivar/citologia , Ratos Long-Evans/anatomia & histologia , Animais , Biotina/análogos & derivados , Tamanho Celular , Dextranos , Feminino , Corantes Fluorescentes , Lateralidade Funcional , Masculino , Terminações Nervosas/anatomia & histologia , Vias Neurais , Células de Purkinje/citologia , Células de Purkinje/ultraestrutura , RatosRESUMO
Bilateral lesions of the central tegmental field (CTF) in male rats virtually eliminate mating behavior. This study examined if mating-induced Fos expression (a measure of neuronal activation) and androgen receptors (AR) are colocalized in brain and spinal cord neurons which project to the CTF. Animals received unilateral injections of the retrograde tracer Fluorogold (FG) in the lateral part of the CTF (CTFl), and 10 days later were killed after ejaculating with females. Brains and spinal cords were examined for FG transport, AR-immunoreactivity (AR-ir), and Fos-immunoreactivity (Fos-ir). AR-ir and Fos-ir were visualized with fluorescence microscopy using cyanine-conjugated and fluorescein-conjugated secondary antibodies. The CTFl received projections from AR-containing neurons in forebrain structures (bed nucleus of stria terminalis, medial preoptic area, lateral and ventromedial hypothalamus), in the central amygdala and various mid- and hindbrain structures (dorsolateral tegmentum, superior and inferior colliculi, pedunculopontine nucleus), and in the lumbosacral spinal cord (lamina X). Some of the AR-containing neurons in bed nucleus of stria terminalis and in the dorsal part of the medial preoptic area with projections to the CTFl were activated by mating. Most AR-containing neurons in spinal lamina X with projections to the CTFl were also activated by mating. Information from spinal cord and pontine nuclei and from outputs descending from the forebrain may be relayed in the CTFl. Thus, as part of a network of hormone-sensitive neurons linking brain and spinal cord mechanisms for mating, the CTFl could participate in the integration of visceral and somatic information relevant for sexual behavior.
Assuntos
Encéfalo/fisiologia , Ejaculação/fisiologia , Neurônios/fisiologia , Proteínas Proto-Oncogênicas c-fos/genética , Ratos Long-Evans/fisiologia , Receptores Androgênicos/metabolismo , Comportamento Sexual Animal/fisiologia , Medula Espinal/fisiologia , Estilbamidinas , Animais , Transporte Axonal , Encéfalo/citologia , Corantes Fluorescentes , Regulação da Expressão Gênica , Genes fos , Masculino , Neurônios/citologia , Especificidade de Órgãos , Proteínas Proto-Oncogênicas c-fos/análise , Ratos , Ratos Long-Evans/anatomia & histologia , Receptores Androgênicos/análise , Medula Espinal/citologia , Tegmento Mesencefálico/fisiologiaRESUMO
The goal of the present study was to characterize the anatomical and neurochemical relationships that the raphe nuclear complex maintains with respect to lateralized and centralized components of the ventricular system. From this investigation, we 1) determined the ipsilateral vs. contralateral distribution of raphe efferents to the ependymal wall of the lateral ventricle, 2) assessed the degree of collateralization of individual ependymal projection neurons to other sites along the ventricular path, 3) compared the topography of raphe neurons that project to the ventricular lining as well as the lumen of the fourth and lateral ventricles, and 4) evaluated the neurochemical identity of raphe neurons that innervate the ventricular system. After tracer injections into the lateral ventricle, labeled cells were distributed evenly on both sides of the midline in the dorsomedial subregion of the intermediate dorsal raphe nucleus. Further rostrally, labeled cells were clustered bilaterally above the medial longitudinal fasciculi and extended into the median raphe nucleus. Injections that involved the ependymal wall of the lateral ventricle resulted in prominent ipsilateral labeling within the dorsal raphe nucleus, just ventral to the cerebral aqueduct. Most of the labeled cells in this latter group had collateral projections to other sites along the ventricular path. Most of the ventricle projection cells contained serotonin but not nicotinamide adenine dinucleotide phosphate diaphorase. These findings indicate that the raphe nuclear complex is topographically organized with respect to the ventricular system. Selected subsets of serotoninergic dorsal raphe neurons may influence discrete segments of the ventricular system independently as well as coordinate functions throughout the system through axon collaterals to other sites along the ventricular neuraxis.