Evidence for a physiological role for nitric oxide in the regulation of the lh surge

Effect of central administration of antisense oligonucleotides to nitric oxide synthase

Kripamoy Aguan, Virendra B. Mahesh, Lin Ping, Ganapathy Bhat, Darrell W Brann

Research output: Contribution to journalArticle

73 Citations (Scopus)

Abstract

Antisense oligonucleotides of brain-nitric oxide synthase (b-NOS) and endothelial-NOS (e-NOS) were used in steroid-primed ovariectomized rats to examine the physiological role of nitric oxide in the regulation of the LH surge. Since macrophage-NOS (m-NOS) is not produced in the hypothalamus under normal conditions, the m-NOS antisense oligonucleotide was used as control for the possible toxicity of the phosphorothioated and propynylated antisense oligonucleotides used. Female rats were ovariectomized on day 70 of age and implanted with a third ventricle cannula on day 77 of age, injected with 5 μg of estradiol on days 84 and 85 of age at 17.00 h and with 1 mg progesterone or vehicle on day 86 at 09.00 h. Blood samples were collected between 13.00 and 19.00 h on day 86 of age via a jugular cannula inserted on day 85 of age. Antisense oligonucleotides (400 or 800 ng) or vehicle were injected in the third ventricle at 17.00 h on days 84 and 85 just before the estradiol injection and at 06.00 and 12.00 h on day 86. Neither the 400-ng nor the 800-ng dose of m-NOS AS had any effect on the steroid-induced LH surge. In contrast, central administration of the 400-ng dose of e-NOS AS and the 800-ng dose of b-NOS AS significantly attenuated the steroid-induced LH surge. The 40% reduction in LH by e-NOS AS and b-NOS AS was accompanied by a 33 and 28% reduction in their respective protein levels as shown by Western blots. The higher amount of b-NOS AS needed to reduce the LH surge is probably due to the high abundance of b-NOS in the hypothalamus as compared to e-NOS. As a whole, this study provides significant evidence for a physiological role of nitric oxide in mediating the steroid-induced LH surge.

Original languageEnglish (US)
Pages (from-to)449-455
Number of pages7
JournalNeuroendocrinology
Volume64
Issue number6
DOIs
StatePublished - Jan 1 1996

Fingerprint

Antisense Oligonucleotides
Nitric Oxide Synthase
Nitric Oxide
Steroids
Brain
Third Ventricle
Macrophages
Hypothalamus
Estradiol
Nitric Oxide Synthase Type III
Progesterone
Neck
Western Blotting
Injections
Proteins
Cannula

Keywords

  • Antisense oligonucleotides
  • Gonadotropins
  • Nitric oxide
  • Nitric oxide synthase
  • Sex steroids

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology
  • Endocrine and Autonomic Systems
  • Cellular and Molecular Neuroscience

Cite this

Evidence for a physiological role for nitric oxide in the regulation of the lh surge : Effect of central administration of antisense oligonucleotides to nitric oxide synthase. / Aguan, Kripamoy; Mahesh, Virendra B.; Ping, Lin; Bhat, Ganapathy; Brann, Darrell W.

In: Neuroendocrinology, Vol. 64, No. 6, 01.01.1996, p. 449-455.

Research output: Contribution to journalArticle

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abstract = "Antisense oligonucleotides of brain-nitric oxide synthase (b-NOS) and endothelial-NOS (e-NOS) were used in steroid-primed ovariectomized rats to examine the physiological role of nitric oxide in the regulation of the LH surge. Since macrophage-NOS (m-NOS) is not produced in the hypothalamus under normal conditions, the m-NOS antisense oligonucleotide was used as control for the possible toxicity of the phosphorothioated and propynylated antisense oligonucleotides used. Female rats were ovariectomized on day 70 of age and implanted with a third ventricle cannula on day 77 of age, injected with 5 μg of estradiol on days 84 and 85 of age at 17.00 h and with 1 mg progesterone or vehicle on day 86 at 09.00 h. Blood samples were collected between 13.00 and 19.00 h on day 86 of age via a jugular cannula inserted on day 85 of age. Antisense oligonucleotides (400 or 800 ng) or vehicle were injected in the third ventricle at 17.00 h on days 84 and 85 just before the estradiol injection and at 06.00 and 12.00 h on day 86. Neither the 400-ng nor the 800-ng dose of m-NOS AS had any effect on the steroid-induced LH surge. In contrast, central administration of the 400-ng dose of e-NOS AS and the 800-ng dose of b-NOS AS significantly attenuated the steroid-induced LH surge. The 40{\%} reduction in LH by e-NOS AS and b-NOS AS was accompanied by a 33 and 28{\%} reduction in their respective protein levels as shown by Western blots. The higher amount of b-NOS AS needed to reduce the LH surge is probably due to the high abundance of b-NOS in the hypothalamus as compared to e-NOS. As a whole, this study provides significant evidence for a physiological role of nitric oxide in mediating the steroid-induced LH surge.",
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