Jahn G A, Deis R P
Laboratorio de Reproducción y Lactancia, LARLAC-CRICYT, Mendoza, Argentina.
J Endocrinol. 1991 Jun;129(3):343-50. doi: 10.1677/joe.0.1290343.
The part played by the adrenergic system on the release of prolactin and lactogenesis induced by prostaglandin F2 alpha and the antiprogesterone RU 486 was studied in pregnant rats. Two doses of prostaglandin F2 alpha (150 micrograms) administered at 08.00 and 12.00 h on day 19 of pregnancy induced, at 12.00 h on day 20 (24 h after administration), a significant increase in the serum concentration of prolactin, with a significant decrease in serum progesterone levels. These hormonal changes significantly augmented casein and lactose levels in the mammary gland. Treatment with RU 486 (2 mg/kg) at 08.00 h on day 19 augmented casein and lactose concentrations in the mammary gland at 12.00 h on day 20 without modifying serum concentrations of prolactin and progesterone. The adrenergic antagonists, propranolol (3 mg/kg), metoprolol (10 mg/kg), ICI 118,551 (200 micrograms/kg), idazoxan (100 micrograms/kg) and prazosin (10 mg/kg), were administered s.c. at 12.00 and 20.00 h on day 19 and 08.00 h on day 20 of pregnancy to intact rats or to rats previously treated with RU 486 or prostaglandin F2 alpha. These adrenergic antagonists did not modify serum prolactin or progesterone levels in intact or RU 486-treated rats, but serum prolactin levels in the prostaglandin F2 alpha-treated group were significantly reduced by treatment with propranolol, metoprolol or prazosin. In addition, propranolol and ICI 118,551 also decreased the casein and lactose concentrations in the mammary glands of RU 486- and prostaglandin F2 alpha-treated rats, while the other compounds had no effect.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了肾上腺素能系统在前列腺素F2α和抗孕酮RU 486诱导的催乳素释放及泌乳生成过程中所起的作用,实验对象为怀孕大鼠。在妊娠第19天的08:00和12:00给予两剂前列腺素F2α(150微克),在第20天的12:00(给药后24小时),血清催乳素浓度显著升高,血清孕酮水平显著降低。这些激素变化显著提高了乳腺中酪蛋白和乳糖的水平。在妊娠第19天的08:00用RU 486(2毫克/千克)进行处理,可使第20天12:00时乳腺中酪蛋白和乳糖浓度升高,而不改变血清催乳素和孕酮的浓度。在妊娠第19天的12:00和20:00以及第20天的08:00,对完整大鼠或先前用RU 486或前列腺素F2α处理过的大鼠皮下注射肾上腺素能拮抗剂普萘洛尔(3毫克/千克)、美托洛尔(10毫克/千克)、ICI 118,551(200微克/千克)、咪唑克生(100微克/千克)和哌唑嗪(10毫克/千克)。这些肾上腺素能拮抗剂在完整大鼠或RU 486处理的大鼠中未改变血清催乳素或孕酮水平,但在前列腺素F2α处理组中,普萘洛尔、美托洛尔或哌唑嗪处理可显著降低血清催乳素水平。此外,普萘洛尔和ICI 118,551还降低了RU 486和前列腺素F2α处理大鼠乳腺中的酪蛋白和乳糖浓度,而其他化合物则无此作用。(摘要截短为250字)