Abstract
The delta opioid peptide [D-Ala(2), D-Leu(5)]enkephalin (DADLE) has been shown to enhance the survival of dopaminergic neurons. Here, we found that chronic treatment with DADLE caused a significant increase in nerve growth factor (NGF) in the hippocampus and the midbrain of adult albino Swiss (CD-1) mice, but not in the striatum or frontal cortex. Glia-derived neurotrophic factor (GDNF) was not significantly affected. Thus, the neuroprotective action of DADLE may be mediated in part by NGF.
Publication types
-
Research Support, U.S. Gov't, P.H.S.
MeSH terms
-
Animals
-
Brain / drug effects*
-
Brain / metabolism
-
Corpus Striatum / drug effects
-
Corpus Striatum / metabolism
-
Enkephalin, Leucine-2-Alanine / pharmacology*
-
Enzyme-Linked Immunosorbent Assay
-
Frontal Lobe / drug effects
-
Frontal Lobe / metabolism
-
Glial Cell Line-Derived Neurotrophic Factor
-
Hippocampus / drug effects
-
Hippocampus / metabolism
-
Injections, Intraperitoneal
-
Mesencephalon / drug effects
-
Mesencephalon / metabolism
-
Mice
-
Nerve Growth Factor / metabolism*
-
Nerve Growth Factors / metabolism
Substances
-
Gdnf protein, mouse
-
Glial Cell Line-Derived Neurotrophic Factor
-
Nerve Growth Factors
-
Enkephalin, Leucine-2-Alanine
-
Nerve Growth Factor