No description available.

ABSTRACT The current study documents the findings from immunohistochemical examination of the brains of microbats and megabats (Chiroptera) using antibodies for cholineacetyltransferase (cholinergic neurons), tyrosine hydroxylase (dopaminergic, adrenergic and noradrenergic neurons), and serotonin (serotonergic neurons). The objective of the study was firstly to describe the anatomical organization and morphology of the neuromodulatory systems (nuclear complement) in both microbats and megabats, as there is no literature on these systems in the brains of chiropterans. Secondly, we aimed to investigate whether or not there are differences in these systems between the two suborders of chiroptera in hopes to shed some light on the phylogeny of the two, which is a controversial subject. The two groups were found to possess clear differences in their respective neuromodulatory nuclear complements. The differences observed between the two groups include a dorsal division of the locus coeruleus (A6d), which was absent in microbats but present in megabats, also the absence of an A4 in microbats but clear presence in megabats, and the parabigeminal (PBg) nucleus that was absent in microbats but clearly visible in megabats. The microbats were found to possess a complement that appeared similar to that of insectivores; whereas megabats had a complement resembling that of primates, carnivores and rodents. The differences found between the two groups suggest a diphyletic origin for the two groups.

The current study uses the head and neck of giraffe (Giraffa camelopardalis) as a model for tracking the course of evolutionary change. Gould (2002) has argued that there are three main avenues of evolutionary change that result in the genesis of new morphologies. These are phylogenetic constraints, structural or allometric scaling laws of form, and specific unique adaptations. It is well known that the unique characteristic of the giraffe is its extremely long neck and yet, it only has seven cervical vertebrae. To study the neck the vertebral body lengths of different aged giraffes were measured to determine the contribution of the cervical vertebrae to the total vertebral column. The vertebrae of several extant ungulates as well as those of fossil giraffids were used as a comparison with the giraffe. CT scans were used on several giraffe skulls to study the extent of the frontal sinus in the giraffe in an attempt to explain why the giraffe evolved such a large frontal sinus. The vertebral columns and skulls of several ungulates, including the okapi (Okapia johnstoni) were also used to compare with the results obtained from the giraffe. Immunohistochemistry was used to study the medulla and spinal cord sections of the giraffe to determine if the location and size of the nuclei remained unchanged to the basic ungulate or mammalian plan in spite of the unusually long neck, or if this long neck led to changes in the nuclei found in those regions. The results of these stains were all compared to the published literature available. Although more studies need to be conducted on other ungulates to conclusively determine why giraffe have evolved a long neck, overall the results showed that the anatomy giraffe head and neck remained true to the basic mammalian plan, with very little changing in terms of it morphology. The giraffe brain and spinal cord also resembled that of a typical ungulate. This leads to the conclusion that constraints and allometric scaling laws of form play a greater role than previously thought in the evolution of extreme morphologies.

A extinção é uma forma de aprendizado inibitório que se origina na omissão do reforço ou estímulo incondicionado, inibindo a evocação de uma resposta ou comportamento aprendido anteriormente. Muitas formas de aprendizado são moduladas por receptores β- noradrenérgicos, D1-dopaminérgicos e H2-histaminérgicos no córtex pré-frontal ventromedial (vmPFC), no complexo basolateral da amígdala (BLA) e no hipocampo dorsal (DH). Assim, o objetivo do presente trabalho foi investigar a modulação da extinção de memória aversiva nestas três regiões cerebrais. Para isso, utilizamos ratos machos Wistar, que foram submetidos ao paradigma de esquiva inibitória (EI) ou condicionamento contextual ao medo (CCM). As diferentes drogas utilizadas foram infundidas através das cânulas guias implantadas estereotaxicamente no DH, BLA ou vmPFC imediatamente após a sessão de extinção e seus efeitos sobre a extinção foram avaliados em uma sessão de teste realizada 24 h depois. A DSerina (50 μg/lado), modulador positivo do receptor NMDA, e o SKF9188 (12.5 μg/lado), inibidor da enzima histamina metil-transferase, melhoraram a consolidação da memória de extinção nas tarefas de EI e CCM. Entretanto, o AP5 (5 μg/lado), antagonista do receptor glutamatérgico NMDA, e a ranitidina (17.5 μg/lado), antagonista do receptor histaminérgico H2, prejudicaram a extinção em ambos os paradigmas, indicando que os receptores glutamatérgicos do tipo NMDA estão envolvidos na consolidação dos dois paradigmas utilizados, e que os receptores histaminérgicos H2 modulam a extinção nas três estruturas estudadas. A noradrenalina (1 μg/lado), o antagonista β-adrenoreceptor, timolol (1 μg/lado), o agonista dos receptores D1, SKF38393 (12.5 μg/lado) e o antagonista dos receptores D1, SCH23390 (1.5 μg/lado) também afetam a extinção nas duas tarefas, porém, seus efeitos são variados dependendo da tarefa e do local da infusão, sugerindo que a modulação da extinção pelos receptores β- e D1 é mais complexa. Nossos resultados mostram que as três estruturas são ativadas durante o processo de extinção da memória e que os sistemas neuromodulatórios atuam de formas distintas nessas tarefas. / Extinction consists of the learned inhibition of retrieval of previously acquired memory. Many forms of learning are modulated by β-noradrenergic, D1-dopaminergic and H2-histaminergic receptors on ventromedial prefrontal cortex (vmPFC), basolateral amygdala (BLA) and dorsal hippocampus. Therefore, the aim of this work was investigated the modulation of aversive memory extinction in these brain structures. Male Wistar rats were submitted to inhibitory avoidance paradigm (EI) or contextual fear conditioning (CCM). The drugs were infused through cannulae implanted into the DH, BLA or vmPFC immediately after the extinction session and their effects were evaluated 24 h later. D-serine (50 μg/side), a NMDA receptor stimulant, and SKF9188 (12.5 μg/side), a histamine methyl-transferase inhibitor, enhanced the consolidation of the extinction memory in EI and CCM tasks. However, AP5 (5 μg/side), a NMDA-antagonist, and ranitidine (17.5 μg/side), a H2- histaminergic antagonist, impaired the extinction of both tasks, indicated that NMDA receptors are involved in the consolidation of extinction of both tasks, and histamine H2 receptors modulate that process in all areas studied. Noradrenaline (1 μg/side), timolol 1 μg/side), a β-adrenergic antagonist, SKF38393 (12.5 μg/side) and SCH23390 (1.5 μg/side), D1 agonist and antagonist receptor, respectively, also affected the extinction, but their effects varied with the task and with the site of infusion, suggesting that extinction modulation by β- and D1 is more complex. In conclusion, the three structures investigated are activated in the aversive memory extinction and the neuromodulatory systems act of different forms in these structures.

A extinção é uma forma de aprendizado inibitório que se origina na omissão do reforço ou estímulo incondicionado, inibindo a evocação de uma resposta ou comportamento aprendido anteriormente. Muitas formas de aprendizado são moduladas por receptores β- noradrenérgicos, D1-dopaminérgicos e H2-histaminérgicos no córtex pré-frontal ventromedial (vmPFC), no complexo basolateral da amígdala (BLA) e no hipocampo dorsal (DH). Assim, o objetivo do presente trabalho foi investigar a modulação da extinção de memória aversiva nestas três regiões cerebrais. Para isso, utilizamos ratos machos Wistar, que foram submetidos ao paradigma de esquiva inibitória (EI) ou condicionamento contextual ao medo (CCM). As diferentes drogas utilizadas foram infundidas através das cânulas guias implantadas estereotaxicamente no DH, BLA ou vmPFC imediatamente após a sessão de extinção e seus efeitos sobre a extinção foram avaliados em uma sessão de teste realizada 24 h depois. A DSerina (50 μg/lado), modulador positivo do receptor NMDA, e o SKF9188 (12.5 μg/lado), inibidor da enzima histamina metil-transferase, melhoraram a consolidação da memória de extinção nas tarefas de EI e CCM. Entretanto, o AP5 (5 μg/lado), antagonista do receptor glutamatérgico NMDA, e a ranitidina (17.5 μg/lado), antagonista do receptor histaminérgico H2, prejudicaram a extinção em ambos os paradigmas, indicando que os receptores glutamatérgicos do tipo NMDA estão envolvidos na consolidação dos dois paradigmas utilizados, e que os receptores histaminérgicos H2 modulam a extinção nas três estruturas estudadas. A noradrenalina (1 μg/lado), o antagonista β-adrenoreceptor, timolol (1 μg/lado), o agonista dos receptores D1, SKF38393 (12.5 μg/lado) e o antagonista dos receptores D1, SCH23390 (1.5 μg/lado) também afetam a extinção nas duas tarefas, porém, seus efeitos são variados dependendo da tarefa e do local da infusão, sugerindo que a modulação da extinção pelos receptores β- e D1 é mais complexa. Nossos resultados mostram que as três estruturas são ativadas durante o processo de extinção da memória e que os sistemas neuromodulatórios atuam de formas distintas nessas tarefas. / Extinction consists of the learned inhibition of retrieval of previously acquired memory. Many forms of learning are modulated by β-noradrenergic, D1-dopaminergic and H2-histaminergic receptors on ventromedial prefrontal cortex (vmPFC), basolateral amygdala (BLA) and dorsal hippocampus. Therefore, the aim of this work was investigated the modulation of aversive memory extinction in these brain structures. Male Wistar rats were submitted to inhibitory avoidance paradigm (EI) or contextual fear conditioning (CCM). The drugs were infused through cannulae implanted into the DH, BLA or vmPFC immediately after the extinction session and their effects were evaluated 24 h later. D-serine (50 μg/side), a NMDA receptor stimulant, and SKF9188 (12.5 μg/side), a histamine methyl-transferase inhibitor, enhanced the consolidation of the extinction memory in EI and CCM tasks. However, AP5 (5 μg/side), a NMDA-antagonist, and ranitidine (17.5 μg/side), a H2- histaminergic antagonist, impaired the extinction of both tasks, indicated that NMDA receptors are involved in the consolidation of extinction of both tasks, and histamine H2 receptors modulate that process in all areas studied. Noradrenaline (1 μg/side), timolol 1 μg/side), a β-adrenergic antagonist, SKF38393 (12.5 μg/side) and SCH23390 (1.5 μg/side), D1 agonist and antagonist receptor, respectively, also affected the extinction, but their effects varied with the task and with the site of infusion, suggesting that extinction modulation by β- and D1 is more complex. In conclusion, the three structures investigated are activated in the aversive memory extinction and the neuromodulatory systems act of different forms in these structures.

A extinção é uma forma de aprendizado inibitório que se origina na omissão do reforço ou estímulo incondicionado, inibindo a evocação de uma resposta ou comportamento aprendido anteriormente. Muitas formas de aprendizado são moduladas por receptores β- noradrenérgicos, D1-dopaminérgicos e H2-histaminérgicos no córtex pré-frontal ventromedial (vmPFC), no complexo basolateral da amígdala (BLA) e no hipocampo dorsal (DH). Assim, o objetivo do presente trabalho foi investigar a modulação da extinção de memória aversiva nestas três regiões cerebrais. Para isso, utilizamos ratos machos Wistar, que foram submetidos ao paradigma de esquiva inibitória (EI) ou condicionamento contextual ao medo (CCM). As diferentes drogas utilizadas foram infundidas através das cânulas guias implantadas estereotaxicamente no DH, BLA ou vmPFC imediatamente após a sessão de extinção e seus efeitos sobre a extinção foram avaliados em uma sessão de teste realizada 24 h depois. A DSerina (50 μg/lado), modulador positivo do receptor NMDA, e o SKF9188 (12.5 μg/lado), inibidor da enzima histamina metil-transferase, melhoraram a consolidação da memória de extinção nas tarefas de EI e CCM. Entretanto, o AP5 (5 μg/lado), antagonista do receptor glutamatérgico NMDA, e a ranitidina (17.5 μg/lado), antagonista do receptor histaminérgico H2, prejudicaram a extinção em ambos os paradigmas, indicando que os receptores glutamatérgicos do tipo NMDA estão envolvidos na consolidação dos dois paradigmas utilizados, e que os receptores histaminérgicos H2 modulam a extinção nas três estruturas estudadas. A noradrenalina (1 μg/lado), o antagonista β-adrenoreceptor, timolol (1 μg/lado), o agonista dos receptores D1, SKF38393 (12.5 μg/lado) e o antagonista dos receptores D1, SCH23390 (1.5 μg/lado) também afetam a extinção nas duas tarefas, porém, seus efeitos são variados dependendo da tarefa e do local da infusão, sugerindo que a modulação da extinção pelos receptores β- e D1 é mais complexa. Nossos resultados mostram que as três estruturas são ativadas durante o processo de extinção da memória e que os sistemas neuromodulatórios atuam de formas distintas nessas tarefas. / Extinction consists of the learned inhibition of retrieval of previously acquired memory. Many forms of learning are modulated by β-noradrenergic, D1-dopaminergic and H2-histaminergic receptors on ventromedial prefrontal cortex (vmPFC), basolateral amygdala (BLA) and dorsal hippocampus. Therefore, the aim of this work was investigated the modulation of aversive memory extinction in these brain structures. Male Wistar rats were submitted to inhibitory avoidance paradigm (EI) or contextual fear conditioning (CCM). The drugs were infused through cannulae implanted into the DH, BLA or vmPFC immediately after the extinction session and their effects were evaluated 24 h later. D-serine (50 μg/side), a NMDA receptor stimulant, and SKF9188 (12.5 μg/side), a histamine methyl-transferase inhibitor, enhanced the consolidation of the extinction memory in EI and CCM tasks. However, AP5 (5 μg/side), a NMDA-antagonist, and ranitidine (17.5 μg/side), a H2- histaminergic antagonist, impaired the extinction of both tasks, indicated that NMDA receptors are involved in the consolidation of extinction of both tasks, and histamine H2 receptors modulate that process in all areas studied. Noradrenaline (1 μg/side), timolol 1 μg/side), a β-adrenergic antagonist, SKF38393 (12.5 μg/side) and SCH23390 (1.5 μg/side), D1 agonist and antagonist receptor, respectively, also affected the extinction, but their effects varied with the task and with the site of infusion, suggesting that extinction modulation by β- and D1 is more complex. In conclusion, the three structures investigated are activated in the aversive memory extinction and the neuromodulatory systems act of different forms in these structures.

The mammalian spinal cord contains the neuronal circuitry necessary to generate rhythmic locomotor activity in the absence of inputs from the higher brain centre or sensory system. This circuitry is regulated by local neuromodulatory inputs, which can adjust the strength and timing of locomotor output. The free radical gas nitric oxide has been shown to act as an important neuromodulator of spinal circuits, which control locomotion in other vertebrate models such as the tadpole and lamprey. Despite this, the involvement of the NO-mediated soluble guanylate cyclase/cyclic guanosine monophosphate secondary messenger-signalling pathway (NO/sGC/cGMP) in mammalian locomotion has largely been under-investigated. The NADPH diaphorase histochemical reaction was used to identify sources of NO in the lumbar spinal cord. The largest population NADPH diaphorase reactive neurons were located in the dorsal horn, followed by the laminae of the ventral horn, particularly around the central canal (lamina X) and lamina VII. NADPH diaphorase reactive neurons were found along a rostrocaudal gradient between lumbar segments L1 to L5. These results show that that discrete neuronal sources of NO are present in the developing mouse spinal cord, and that these cells increase in number during the developmental period postnatal day P1 – P12. NADPH diaphorase was subsequently used to identify NADPH diaphorase reactive neurons at P12 in the mouse model of ALS using the SODG93A transgenic mouse. Physiological recordings of ventral root output were made to assess the contribution of NO to the regulation induced rhythmic fictive locomotion in the in vitro isolated spinal cord preparation. Exogenous NO inhibits central pattern generator (CPG) output while facilitating and inhibiting motor neuron output at low and high concentrations respectively. Removal of endogenous NO increases CPG output while decreasing motor neuron output and these effects are mediated by cGMP. These data suggest that an endogenous tone of NO is involved in the regulation of fictive locomotion and that this involves the NO/sGC/cGMP pathway. Intracellular recordings from presumed motor neurons and a heterogeneous, unidentified sample of interneurons shows that NO modulates the intrinsic properties of spinal neurons. These data suggest that the net effect of NO appears to be a reduction in motor neuron excitability.

No description available.