Abstract |
Neuroprotective effects of androgens have not been well-characterized, but there is evidence that 5 alpha-androstane-3 alpha, 17 beta-diol (3 alpha-diol) has anti-seizure effects. To further examine androgens' neuroprotective effects, testosterone (T), dihydrotestosterone (DHT), 3 alpha-diol (1.0 mg/kg SC daily), or sesame oil vehicle was administered to adrenalectomized or sham-operated, young, female Long Evans rats (N = 52). After seven days, animals were perfused and trunk blood was collected for radioimmunoassay of plasma corticosterone and androgens. No pyknotic cells were seen in the dentate of the sham-operated animals or those animals that had incomplete adrenalectomies (n = 20); however, cresyl violet and TUNEL stains revealed pyknotic cells in the granule layer of the dentate gyrus of adrenalectomized rats (n = 28). Testosterone, DHT, or 3 alpha-diol significantly reduced the number of pyknotic cells in the dentate gyrus compared to vehicle administered, adrenalectomized rats. Steroid-administered animals had levels of T, DHT, or 3 alpha-diol within physiological concentrations. These findings suggest that T, DHT, or 3 alpha-diol may have neuroprotective effects via a common mechanism of action.
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Authors | C A Frye, C M McCormick |
Journal | Stress (Amsterdam, Netherlands)
(Stress)
Vol. 3
Issue 3
Pg. 185-94
(May 2000)
ISSN: 1025-3890 [Print] England |
PMID | 10938579
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Neuroprotective Agents
- Dihydrotestosterone
- Androstane-3,17-diol
- Testosterone
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Topics |
- Adrenalectomy
- Analysis of Variance
- Androstane-3,17-diol
(pharmacology)
- Animals
- Apoptosis
(drug effects, physiology)
- Cell Count
(drug effects)
- Dentate Gyrus
(cytology, drug effects, metabolism)
- Dihydrotestosterone
(pharmacology)
- Female
- In Situ Nick-End Labeling
- Neurons
(cytology, drug effects)
- Neuroprotective Agents
(pharmacology)
- Radioimmunoassay
- Rats
- Rats, Long-Evans
- Testosterone
(metabolism, pharmacology)
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