Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    In: Neuroembryology and Aging, S. Karger AG, Vol. 3, No. 2 ( 2004), p. 92-98
    Abstract: 〈 i 〉 Background: 〈 /i 〉 Nitric oxide synthase (NOS) produces nitric oxide (NO) from arginine, and both NOS and NO play important roles in the normal aging of the hippocampus. 〈 i 〉 Aim: 〈 /i 〉 To study the age-related distribution patterns of the neuronal (nNOS) and the inducible (iNOS) isoforms of NOS in the mouse hippocampus, and their roles in the aging mechanism. 〈 i 〉 Result: 〈 /i 〉 The nNOS significantly decreased in the aged hippocampus whereas iNOS increased significantly. The nNOS expressed in interneuron-like cells distributed mainly in the dentate gyrus and the pyramidal layer. iNOS was possibly expressed in both old and newly proliferated astrocytes mainly found in the stratum oriens, stratum lacunosum-moleculare and to a lesser extent in the fimbria and dentate gyrus. The astrocyte number also significantly increased in the aged hippocampus. In fact, iNOS was almost absent in the young hippocampus. Those cells expressing the two isoforms were not apoptotic. 〈 i 〉 Conclusion: 〈 /i 〉 The results suggested different expression patterns for nNOS and iNOS during aging in terms of the localization, expression levels and cell types involved. These changes were unlikely to involve apoptosis. This might signify an alteration in the normal functions of the hippocampus during aging such as long-term potentiation.
    Type of Medium: Online Resource
    ISSN: 1661-3406 , 1661-3414
    Language: English
    Publisher: S. Karger AG
    Publication Date: 2004
    detail.hit.zdb_id: 2206059-5
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. Further information can be found on the KOBV privacy pages