By Sudarshan K. Malhotra
A part of a sequence which goals to hide contemporary wisdom within the box of neural technological know-how, this quantity discusses such themes as: the molecular bases of nerve regeneration; plasticity of descending spinal pathways in constructing mammals; and improvement of the mammalian auditory hindbrain.
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As described earlier in this review, the ontogenesis of most peptidergic neurons in the CNS occurs early in development and coincides with the period of neural crest migration. The evidence supporting the notion of a peptide influence on neuronal phenotypic expression is accumulating as researchers pursue the exact identity of these peptide factors. , 1985). Dal Toso et al. (1988) have identified a basic neurono- Neuropeptides in Development 33 trophic protein of 14 kDa derived from the striatum.
5 days) in the chick embryo. We have found catecholaminergic expression as early as E4 in the avian model system, using TH activity as a biochemical marker for catecholaminergic neurons (Kentroti and Vernadakis, 1989). Recently we have found that the critical period for neuroblasts to respond to GHRH is between E 1 and E3 in the chick, a period characterized by active neuronal proliferation and differentiation (Bennett and DiLullo, 1985a, b). , 1982). Embryos treated with GHRH in ovo on embryonic days 1,3, 5, and 7 exhibit a significant increase in TH activity.
Specific SRIF receptors are first detected at E 15, reach a maximum at P 13, and gradually decline between P 13 and P23. Virtually no SRIF receptors can be detected in the adult rat cerebellum. , 1990) characterized the SRIF receptors in the immature (13-day-old) rat cerebellum using membrane enriched preparations and autoradiography for binding of two ligands, 125I-Tyr~ D-Trp 8 SRIF-14 and 125I-SMS 204-090. The pharmacological profiles observed are similar to that of 22 SUSAN KENTROTI and ANTONIA VERNADAKIS adult rat cortex.
Advances in Neural Science, Volume 2 (Advances in Neural Science) by Sudarshan K. Malhotra