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Energy Dependency of Glucocorticoid Exacerbation of gp120 Neurotoxicity
Author(s) -
Brooke Sheila M.,
Howard Sarah A.,
Sapolsky Robert M.
Publication year - 1998
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.1998.71031187.x
Subject(s) - neurotoxicity , hippocampal formation , nmda receptor , glucocorticoid , biology , neurotoxin , calcium , glucocorticoid receptor , pharmacology , medicine , endocrinology , chemistry , receptor , toxicity
The HIV envelope glycoprotein, gp120, a well documented neurotoxin, may be involved in AIDS‐related dementia complex. gp120 works through an NMDA receptor‐ and calcium‐dependent mechanism to damage neurons. We have previously demonstrated that both natural and synthetic glucocorticoids (GCs) exacerbate gp120‐induced neurotoxicity and calcium mobilization in hippocampal mixed cultures. GCs, steroid hormones secreted during stress, are now shown to work in conjunction with gp120 to decrease ATP levels and to work synergistically with gp120 to decrease the mitochondrial potential in hippocampal cultures. Furthermore, energy supplementation blocked the ability of GCs to worsen gp120's effects on neuronal survival and calcium mobilization. A GC‐induced reduction in glucose transport in hippocampal neurons, as previously documented, may contribute to this energetic dependency. These results may have clinical significance, considering the common treatment of severe cases of Pneumocystis carinii pneumonia, typical of HIV infection, with large doses of synthetic GCs.