PubMed Health⌕ Search

PubMed · 12143390

Neuronal changes during development and evolution (an overview).

Abstract

This overview highlights the presentations made by several authors, with sidelights commentaries on the topics covered in this session. The Neurotropic hypothesis, formulated by Cajal more than one century ago, has been one of the fundamental tenets of modern Neuroscience. Research work is unveiling highly complex molecular mechanisms by means of which neuronal processes grow in the right direction leading to the formation of neural networks. Another interesting topic covered in this session pertains to the remarkably conserved similarity of most parts of the brain between reptiles, birds and mammals. The presence of the neocortex, which occurs in mammals, is discussed on the basis of different migratory behavior during development. The question of neuronal stability throughout the life cycle raises interesting aspects on the generation of new neurons. This is a particularly timely topic because recent evidence, denied by others, has shown the generation of new neocortical neurons in the adult. In another session, it was discussed the evidence showing that pyramidal cells and intrinsic cells of the neocortex have different developmental origins. Finally, several modern analyses show the role of different transcription factors in the formation of brain cortical maps before the arrival of their proper afferent connections.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Facundo Valverde. 2002. Neuronal changes during development and evolution (an overview).. https://doi.org/10.1016/s0079-6123(02)36003-5

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Anterograde transneuronal viral tracing of central viscerosensory pathways in rats.

Previous studies demonstrated that strain H129 of herpes simplex virus-1 undergoes anterograde transneuronal transport in mice and primates after peripheral or central injection. In this study, H129 was used in rats to identify CNS regions that receive relayed viscero-sensory inputs from the stomach wall. We also examined whether transneuronal viral transport in this model is exclusively anterograde. H129 or an established retrograde transneuronal viral tracer, pseudorabies virus (PRV), was injected into the ventral stomach wall in intact rats or in rats with previous subdiaphragmatic vagal sensory deafferentation. Rats were perfused with fixative 3-5 d later, and tissues were processed for immunocytochemical detection of transported virus. In intact rats, H129 was transported transneuronally via vagal and spinal viscerosensory neurons to postsynaptic target cells in the medullary dorsal vagal complex and thoracic dorsal horn, respectively, with subsequent transport to discrete regions of the medullary and pontine reticular formation, cerebellum, parabrachial nucleus, periaqueductal gray, thalamus, hypothalamus, amygdala, bed nucleus of the stria terminalis, and other central sites. Comparison of labeling patterns in intact and vagal deafferented rats indicated that H129 also produced first-order retrograde infection of autonomic neurons that project directly to virus injection sites, similar to PRV. Unlike PRV, however, H129 was not transported transneuronally in the retrograde direction from infected neurons to central sources of presynaptic input. We conclude that transneuronal transport of H129 occurs exclusively in the anterograde direction to reveal CNS regions that receive direct and relayed viscerosensory signals.

Afferent Pathways↗

Differential effects of hindlimb peripheral afferents on motoneurons innervating different parts of longissimus muscle in cats.

Previous studies (Wada and Kanda 2001, Exp Brain Res 136:263-263; Wada et al. 1999, Exp Brain Res 128:543-549) demonstrated that input patterns from hindlimb muscles and cutaneous afferents vary among individual trunk muscle motoneurons. The purpose of the present study was to examine the relationship between the synaptic pattern from hindlimb afferents and the area innervated by motoneurons. Histologic study of m. longissimus lumborum (Long) indicated that the distribution of different fiber types (slow-twitch oxidative, SO; fast-twitch oxidative glycolytic, FOG; fast-twitch glycolytic, FG) depends on the area of the Long cross-section. The ventromedial area and dorsolateral area of the cross-section possess a high content of SO and FG, respectively. The motoneurons innervating the dorsolateral area receive muscle afferent inputs mainly from the ipsilateral side, while the motoneurons innervating the ventromedial area often receive bilateral afferent inputs. The motoneurons innervating the dorsolateral area receive excitatory post-synaptic potentials from cutaneous nerves on both sides. These findings indicate that the effects of afferent inputs from the hindlimbs are related to motoneuron type or the area innervated by the motoneurons.

Afferent Pathways↗

Neurochemical characterization of extrinsic innervation of the guinea pig rectum.

The presence of markers for parasympathetic, sympathetic, and glutamatergic or peptidergic sensory innervation was investigated by using in vitro tracing with biotinamide, combined with immunohistochemistry, to characterise quantitatively extrinsic axons to myenteric ganglia of the guinea pig rectum. Of biotinamide-filled varicose axons, 3.6 +/- 1.3% were immunoreactive for tyrosine hydroxylase (TH) and 16.0 +/- 4.8% for vesicular acetylcholine transporter (VAChT). TH and vesicular monoamine transporter (VMAT1) showed high coexistence (83-100%), indicating that varicosities lacking TH immunoreactivity also lacked VMAT1. VAChT was detectable in 77% of choline acetyltransferase (ChAT)-immunoreactive varicosities. Calcitonin gene-related peptide (CGRP) was detected in 5.3 +/- 1.6% of biotinamide-labeled varicosities, the vesicular glutamate transporter (VGluT) 1 in 2.8 +/- 0.8%, and VGluT2 in 11.3 +/- 4.2% of varicosities of extrinsic origin. Varicosities from the same axon showed consistent immunoreactivity. A novel type of nerve ending was identified, with branching, flattened lamellar endings, similar to the intraganglionic laminar endings (IGLEs) of the proximal gut. Rectal IGLEs were frequently immunoreactive for VGluT1 and VGluT2. Thus most varicose axons of extrinsic origin, which innervate rectal myenteric ganglia, lack detectable levels of immunoreactivity for TH, VMAT1, VAChT, ChAT, VGluT1/2, or CGRP, under conditions in which these markers are readily detectable in other axons. Although some unlabeled varicosities may belong to afferent axons that lack detectable CGRP or VGluT1/2 in the periphery, this suggests that a large proportion of axons do not release any of the major autonomic or sensory transmitters. We speculate that this may vary under particular circumstances, for example, inflammation or obstruction of the gut.

Afferent Pathways↗