Androgens regulate aromatase cytochrome P450 messenger ribonucleic acid in rat brain

Salah E. Abdelgadir, John A. Resko, Sergio Ojeda, Edwin D. Lephart, Michael J. Mcphaul, Charles Roselli

Research output: Contribution to journalArticle

171 Citations (Scopus)

Abstract

The conversion of androgens to estrogens by aromatase cytochrome P450 (P450(AROM)) is an important step in the mechanism of androgen action in the brain. In adult rats, P450(AROM) activity (AA) is regulated by androgens in the preoptic area and medial basal hypothalamus, but is constitutive in the amygdala. This study was undertaken to determine the distribution of P450(AROM) messenger RNA (mRNA) and AA in adult rat brain and examine the effects of steroid treatments on their concentrations in various brain regions. AA was determined by a sensitive assay that measures the production of 3H2O during the conversion of [1β-3H]androstenedione to estrone. P450(AROM) mRNA was measured by a ribonuclease protection assay using a RNA probe complementary to the 5'-coding region of rat P450(AROM) mRNA. The 32P-labeled P450(AROM) probe protected two mRNA fragments in brain tissues that expressed AA (preoptic area, medial basal hypothalamus, amygdala, and hippocampus). The larger protected RNA fragment was 430 nucleotides (nt) long and corresponded in size to the full-length protected complementary RNA, whereas the shorter protected RNA fragment was 300 nt long. Brain tissues that did not exhibit AA contained either the smaller protected RNA fragment (cingulate and parietal cortex) or no protected RNA (cerebellum). These results suggest that the 430-nt protected RNA fragment represents mRNA that encodes the functional P450(AROM) enzyme. In agreement with this conclusion, we found that immature rat ovaries that were stimulated with PMSG to synthesize estrogen contained only the 430-nt protected fragment. The levels of the 430-nt protected RNA fragment differed significantly between brain regions (amygdala >> preoptic area ≥ medial basal hypothalamus ≥ hippocampus) and were significantly correlated with AA (r = 0.994; P <0.001). After castration, the concentrations of P450(AROM) mRNA and AA decreased significantly in the preoptic area and medial basal hypothalamus (P <0.05), but not in the amygdala. Treatments with testosterone or dihydrotestosterons maintained P450(AROM) mRNA and AA at levels approximating those found in intact males. Although 17β-estradiol treatment increased AA in the preoptic area, it did not affect the P450(AROM) mRNA content. These results suggest that the increase in AA observed after exposure to androgens results from regulation of the transcription and/or stability of P450(AROM) mRNA. In contrast, estradiol appears to exert an effect on AA at the posttranscriptional level. Our results also indicate that the levels of P450(AROM) mRNA and AA are heterogeneously distributed in different regions of the brain and appear to be under different modes of regulation in the amygdala compared to the preoptic area and medial basal hypothalamus. The identity of the 300-nt RNA fragment is not yet known, but it may represent an alternately spliced form of P450(AROM) mRNA. Its presence in rat brain, which is not associated with AA, suggests that caution is warranted when measuring P450(AROM) mRNA by methods unable to distinguish between these different RNA transcripts.

Original languageEnglish (US)
Pages (from-to)395-401
Number of pages7
JournalEndocrinology
Volume135
Issue number1
DOIs
StatePublished - Jul 1994

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Aromatase
Cytochrome P-450 Enzyme System
Androgens
RNA
Messenger RNA
Preoptic Area
Middle Hypothalamus
Brain
Amygdala
Nucleotides
Estradiol
Hippocampus
Estrogens
RNA Probes
Complementary RNA
Parietal Lobe
Androstenedione
Estrone
Castration
Gyrus Cinguli

ASJC Scopus subject areas

  • Endocrinology
  • Endocrinology, Diabetes and Metabolism

Cite this

Androgens regulate aromatase cytochrome P450 messenger ribonucleic acid in rat brain. / Abdelgadir, Salah E.; Resko, John A.; Ojeda, Sergio; Lephart, Edwin D.; Mcphaul, Michael J.; Roselli, Charles.

In: Endocrinology, Vol. 135, No. 1, 07.1994, p. 395-401.

Research output: Contribution to journalArticle

Abdelgadir, Salah E. ; Resko, John A. ; Ojeda, Sergio ; Lephart, Edwin D. ; Mcphaul, Michael J. ; Roselli, Charles. / Androgens regulate aromatase cytochrome P450 messenger ribonucleic acid in rat brain. In: Endocrinology. 1994 ; Vol. 135, No. 1. pp. 395-401.
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abstract = "The conversion of androgens to estrogens by aromatase cytochrome P450 (P450(AROM)) is an important step in the mechanism of androgen action in the brain. In adult rats, P450(AROM) activity (AA) is regulated by androgens in the preoptic area and medial basal hypothalamus, but is constitutive in the amygdala. This study was undertaken to determine the distribution of P450(AROM) messenger RNA (mRNA) and AA in adult rat brain and examine the effects of steroid treatments on their concentrations in various brain regions. AA was determined by a sensitive assay that measures the production of 3H2O during the conversion of [1β-3H]androstenedione to estrone. P450(AROM) mRNA was measured by a ribonuclease protection assay using a RNA probe complementary to the 5'-coding region of rat P450(AROM) mRNA. The 32P-labeled P450(AROM) probe protected two mRNA fragments in brain tissues that expressed AA (preoptic area, medial basal hypothalamus, amygdala, and hippocampus). The larger protected RNA fragment was 430 nucleotides (nt) long and corresponded in size to the full-length protected complementary RNA, whereas the shorter protected RNA fragment was 300 nt long. Brain tissues that did not exhibit AA contained either the smaller protected RNA fragment (cingulate and parietal cortex) or no protected RNA (cerebellum). These results suggest that the 430-nt protected RNA fragment represents mRNA that encodes the functional P450(AROM) enzyme. In agreement with this conclusion, we found that immature rat ovaries that were stimulated with PMSG to synthesize estrogen contained only the 430-nt protected fragment. The levels of the 430-nt protected RNA fragment differed significantly between brain regions (amygdala >> preoptic area ≥ medial basal hypothalamus ≥ hippocampus) and were significantly correlated with AA (r = 0.994; P <0.001). After castration, the concentrations of P450(AROM) mRNA and AA decreased significantly in the preoptic area and medial basal hypothalamus (P <0.05), but not in the amygdala. Treatments with testosterone or dihydrotestosterons maintained P450(AROM) mRNA and AA at levels approximating those found in intact males. Although 17β-estradiol treatment increased AA in the preoptic area, it did not affect the P450(AROM) mRNA content. These results suggest that the increase in AA observed after exposure to androgens results from regulation of the transcription and/or stability of P450(AROM) mRNA. In contrast, estradiol appears to exert an effect on AA at the posttranscriptional level. Our results also indicate that the levels of P450(AROM) mRNA and AA are heterogeneously distributed in different regions of the brain and appear to be under different modes of regulation in the amygdala compared to the preoptic area and medial basal hypothalamus. The identity of the 300-nt RNA fragment is not yet known, but it may represent an alternately spliced form of P450(AROM) mRNA. Its presence in rat brain, which is not associated with AA, suggests that caution is warranted when measuring P450(AROM) mRNA by methods unable to distinguish between these different RNA transcripts.",
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AU - Abdelgadir, Salah E.

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N2 - The conversion of androgens to estrogens by aromatase cytochrome P450 (P450(AROM)) is an important step in the mechanism of androgen action in the brain. In adult rats, P450(AROM) activity (AA) is regulated by androgens in the preoptic area and medial basal hypothalamus, but is constitutive in the amygdala. This study was undertaken to determine the distribution of P450(AROM) messenger RNA (mRNA) and AA in adult rat brain and examine the effects of steroid treatments on their concentrations in various brain regions. AA was determined by a sensitive assay that measures the production of 3H2O during the conversion of [1β-3H]androstenedione to estrone. P450(AROM) mRNA was measured by a ribonuclease protection assay using a RNA probe complementary to the 5'-coding region of rat P450(AROM) mRNA. The 32P-labeled P450(AROM) probe protected two mRNA fragments in brain tissues that expressed AA (preoptic area, medial basal hypothalamus, amygdala, and hippocampus). The larger protected RNA fragment was 430 nucleotides (nt) long and corresponded in size to the full-length protected complementary RNA, whereas the shorter protected RNA fragment was 300 nt long. Brain tissues that did not exhibit AA contained either the smaller protected RNA fragment (cingulate and parietal cortex) or no protected RNA (cerebellum). These results suggest that the 430-nt protected RNA fragment represents mRNA that encodes the functional P450(AROM) enzyme. In agreement with this conclusion, we found that immature rat ovaries that were stimulated with PMSG to synthesize estrogen contained only the 430-nt protected fragment. The levels of the 430-nt protected RNA fragment differed significantly between brain regions (amygdala >> preoptic area ≥ medial basal hypothalamus ≥ hippocampus) and were significantly correlated with AA (r = 0.994; P <0.001). After castration, the concentrations of P450(AROM) mRNA and AA decreased significantly in the preoptic area and medial basal hypothalamus (P <0.05), but not in the amygdala. Treatments with testosterone or dihydrotestosterons maintained P450(AROM) mRNA and AA at levels approximating those found in intact males. Although 17β-estradiol treatment increased AA in the preoptic area, it did not affect the P450(AROM) mRNA content. These results suggest that the increase in AA observed after exposure to androgens results from regulation of the transcription and/or stability of P450(AROM) mRNA. In contrast, estradiol appears to exert an effect on AA at the posttranscriptional level. Our results also indicate that the levels of P450(AROM) mRNA and AA are heterogeneously distributed in different regions of the brain and appear to be under different modes of regulation in the amygdala compared to the preoptic area and medial basal hypothalamus. The identity of the 300-nt RNA fragment is not yet known, but it may represent an alternately spliced form of P450(AROM) mRNA. Its presence in rat brain, which is not associated with AA, suggests that caution is warranted when measuring P450(AROM) mRNA by methods unable to distinguish between these different RNA transcripts.

AB - The conversion of androgens to estrogens by aromatase cytochrome P450 (P450(AROM)) is an important step in the mechanism of androgen action in the brain. In adult rats, P450(AROM) activity (AA) is regulated by androgens in the preoptic area and medial basal hypothalamus, but is constitutive in the amygdala. This study was undertaken to determine the distribution of P450(AROM) messenger RNA (mRNA) and AA in adult rat brain and examine the effects of steroid treatments on their concentrations in various brain regions. AA was determined by a sensitive assay that measures the production of 3H2O during the conversion of [1β-3H]androstenedione to estrone. P450(AROM) mRNA was measured by a ribonuclease protection assay using a RNA probe complementary to the 5'-coding region of rat P450(AROM) mRNA. The 32P-labeled P450(AROM) probe protected two mRNA fragments in brain tissues that expressed AA (preoptic area, medial basal hypothalamus, amygdala, and hippocampus). The larger protected RNA fragment was 430 nucleotides (nt) long and corresponded in size to the full-length protected complementary RNA, whereas the shorter protected RNA fragment was 300 nt long. Brain tissues that did not exhibit AA contained either the smaller protected RNA fragment (cingulate and parietal cortex) or no protected RNA (cerebellum). These results suggest that the 430-nt protected RNA fragment represents mRNA that encodes the functional P450(AROM) enzyme. In agreement with this conclusion, we found that immature rat ovaries that were stimulated with PMSG to synthesize estrogen contained only the 430-nt protected fragment. The levels of the 430-nt protected RNA fragment differed significantly between brain regions (amygdala >> preoptic area ≥ medial basal hypothalamus ≥ hippocampus) and were significantly correlated with AA (r = 0.994; P <0.001). After castration, the concentrations of P450(AROM) mRNA and AA decreased significantly in the preoptic area and medial basal hypothalamus (P <0.05), but not in the amygdala. Treatments with testosterone or dihydrotestosterons maintained P450(AROM) mRNA and AA at levels approximating those found in intact males. Although 17β-estradiol treatment increased AA in the preoptic area, it did not affect the P450(AROM) mRNA content. These results suggest that the increase in AA observed after exposure to androgens results from regulation of the transcription and/or stability of P450(AROM) mRNA. In contrast, estradiol appears to exert an effect on AA at the posttranscriptional level. Our results also indicate that the levels of P450(AROM) mRNA and AA are heterogeneously distributed in different regions of the brain and appear to be under different modes of regulation in the amygdala compared to the preoptic area and medial basal hypothalamus. The identity of the 300-nt RNA fragment is not yet known, but it may represent an alternately spliced form of P450(AROM) mRNA. Its presence in rat brain, which is not associated with AA, suggests that caution is warranted when measuring P450(AROM) mRNA by methods unable to distinguish between these different RNA transcripts.

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