Literature DB >> 10478945

NADPH-diaphorase activity in normally developing and intracranially transplanted retinas.

S T Chen1, J P Wang, C L Shen, L S Jen.   

Abstract

The activity and distribution of nicotinamide dinucleotide phosphate diaphorase (NADPH-d), an enzyme that is widely distributed in the central nervous system and involved in the production of the free radical nitric oxide, were investigated histochemically in the normal developing and intracranially transplanted retinas. In the normal rat retina, NADPH-d activity was first detected in cells in the ganglion cells layer (GCL) and blood vessels on the first postnatal day (P0). A small but distinct population of NADPH-d positive cells were observed along the inner border of the inner nuclear layer at P7. NADPH-d positive sublaminae began to appear in the inner plexiform layer during the second postnatal week, and several strongly reactive sublaminae resembling those observed in the adult were observed by the fourth postnatal week. The overall spatio- temporal sequence of development of NADPH-d positive cells in the transplanted retina was similar to that of the normal retina, except a lack of reactive in the inner plexiform layer in more mature transplants as compared with normal retinas of corresponding ages. These results indicate that the time course of development and distribution of NADPH-d cells in early postnatal retina requires signals mainly of intraretinal origin and is independent of influence from the surroundings. While this finding is supportive to the notion that neurons that are rich in NADPH-d are resistant to injury or perturbation, the observation of a lack of well organized NADPH-d reactive sublaminae in the inner plexiform layer in older transplants suggests a possible alteration in the synaptic circuitry in the inner retina with increasing postgrafting survival time.

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Year:  1999        PMID: 10478945     DOI: 10.1023/a:1021013011808

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  29 in total

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Authors:  D S Bredt; S H Snyder
Journal:  Neuron       Date:  1992-01       Impact factor: 17.173

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Authors:  L S Jen; D Tsang; R M Chau; W Z Shen
Journal:  Brain Res       Date:  1990-07-16       Impact factor: 3.252

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Authors:  X X Yan; L J Garey; L S Jen
Journal:  Cereb Cortex       Date:  1996 Sep-Oct       Impact factor: 5.357

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Authors:  J I Patel; S M Gentleman; L S Jen; L J Garey
Journal:  Brain Res       Date:  1997-06-27       Impact factor: 3.252

5.  Role of the target in directing the outgrowth of retinal axons: transplants reveal surface-related and surface-independent cues.

Authors:  M H Hankin; R D Lund
Journal:  J Comp Neurol       Date:  1987-09-15       Impact factor: 3.215

6.  Light-evoked cortical activity produced by illumination of intracranial retinal transplants: experimental studies in rats.

Authors:  S L Craner; J D Radel; L S Jen; R D Lund
Journal:  Exp Neurol       Date:  1989-05       Impact factor: 5.330

7.  NADPH diaphorase histochemistry in the rabbit retina.

Authors:  S M Sagar
Journal:  Brain Res       Date:  1986-05-14       Impact factor: 3.252

8.  Localisation of neuronal nitric oxide synthase-immunoreactivity in rat and rabbit retinas.

Authors:  M T Perez; B Larsson; P Alm; K E Andersson; B Ehinger
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

9.  Nitric oxide-mediated death of cultured neonatal retinal ganglion cells: neuroprotective properties of glutamate and chondroitin sulfate proteoglycan.

Authors:  K A Nichol; M W Schulz; M R Bennett
Journal:  Brain Res       Date:  1995-10-30       Impact factor: 3.252

10.  At least two mechanisms are involved in the death of retinal ganglion cells following target ablation in neonatal rats.

Authors:  Q Cui; A R Harvey
Journal:  J Neurosci       Date:  1995-12       Impact factor: 6.167

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