Collateral sprouting of central noradrenergic neurons during aging: Histochemical and neurochemical studies in intraocular triple transplants

Nisha Srivastava, Ann Charlotte Granholm, Greg A. Gerhardt

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7 Scopus citations

Abstract

The sprouting capacity of aged noradrenergic neurons of the brain-stem nucleus locus coeruleus (LC) was examined using intraocular transplants of fetal tissues. Fetal hippocampal tissue (E18) and LC tissue (E15) were transplanted together as a double transplant into the anterior chamber of the eye of young adult Fischer 344 rats. The double transplants were allowed to mature for 14-18 months, after which an additional fetal hippocampal transplant was placed next to the LC graft. The triple transplants were monitored for overall growth and vascularization for an additional 2-6 months. Immunohistochemical examinations showed that both young (2-6 months old) and aged (16-24 months old) hippocampal cografts contained a plexus of thin varicose tyrosine hydroxylase (TH)-immunoreactive fibers extending throughout the grafted hippocampal tissues. However, the aged hippocampal grafts contained a denser uniform plexus of TH-positive fibers compared to the young transplants. Immunohistochemistry with synapsin antibodies demonstrated that both the young and the aged hippocampal transplants contained much higher densities of synaptic elements than the LC grafts. In vivo electrochemical measurements of potassium-evoked overflow of norepinephrine (NE) in the grafts showed that similar amounts of NE overflow were detected in both the young and the aged hippocampal grafts. HPLC-EC measurements of NE levels in the grafts revealed that there were similar amounts of NE in the young and the aged grafts, and the grafts did not contain serotonin or dopamine. In summary, the findings of the present study show that aged LC neurons are capable of undergoing collateral sprouting producing a functional NE neuronal system when introduced to an appropriate young target.

Original languageEnglish
Pages (from-to)524-535
Number of pages12
JournalExperimental Neurology
Volume145
Issue number2 I
DOIs
StatePublished - Jun 1997

Bibliographical note

Funding Information:
We thank Justin Mott for expert technical assistance with the microphotography. We thank Dr. Doris Dahl, Department of Neuropathology, VA Medical Center, West Roxbury, Massachusetts, for supplying the GFAP antibody and Dr. Michael Browning, Department of Pharmacology, UCHSC, Denver, Colorado, for supplying the synap-sin I and II antibodies. This work was supported by USPHS Grants AG12122 and MH49661 to A.C.G. and AG-06434 and NS09199 to G.A.G. Dr. Gerhardt received support from a Level II National Research Service Scientific Development Award (MH01245). Dr. Srivastava was supported by a fellowship from a Drug Abuse training grant (5T32AAO7464-20).

ASJC Scopus subject areas

  • Neurology
  • Developmental Neuroscience

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