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恒河猴黄体产生前列腺素:孵育条件的特征及假定调节因子的检测

Prostaglandin production by corpora lutea of rhesus monkeys: characterization of incubation conditions and examination of putative regulators.

作者信息

Johnson M S, Ottobre A C, Ottobre J S

机构信息

Department of Dairy Science, College of Agriculture, Ohio State University, Columbus 43210.

出版信息

Biol Reprod. 1988 Nov;39(4):839-46. doi: 10.1095/biolreprod39.4.839.

Abstract

Prostaglandins (PGs) are produced by the corpus luteum (CL) of many domestic and laboratory species and may play a role in CL regulation. The production of PGs by luteal tissue of the rhesus monkey has yet to be clearly elucidated. The production of PGE2, PGF2 alpha, and 6-keto-PGF1 alpha by CL from rhesus monkeys and the incubation conditions (time and cell number) that permit assessment of their synthesis were examined. CL (n = 3 per characterization) were surgically removed from nonpregnant monkeys during the mid-luteal phase of the menstrual cycle (approximately 8-10 days after ovulation). Luteal tissue was dissociated and the cells were incubated at varying concentrations for increasing periods of time at 37 degrees C. Subsequent to defining incubation conditions, various exogenous factors were examined for their potential to modify PG production. Indomethacin, calcium ionophore, human chorionic gonadotropin (hCG), estradiol-17 beta (E2), progesterone (P), testosterone (T), dihydrotestosterone (DHT), and 1-4-6 androstatriene-3, 17-dione (ATD) were incubated with luteal cells in increasing doses. PG and P concentrations in the medium were determined by radioimmunoassay. PGs in the medium after 6 h incubation were detectable at all cell concentrations tested (50,000, 100,000, 200,000 cells/tube). Concentrations of PGs and P increased with cell number (p less than 0.05). Luteal cells (50,000 cells/tube) were incubated for times of 0-24 h. Concentrations of P, PGE2, and PGF2 alpha in the medium were relatively low prior to incubation (0 h), increased (p less than 0.05) linearly within the first 6-12 h, and plateaued through the remaining 24 h.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

前列腺素(PGs)由许多家养及实验动物的黄体(CL)产生,可能在黄体调节中发挥作用。恒河猴黄体组织中PGs的产生情况尚未完全阐明。本研究检测了恒河猴黄体中前列腺素E2(PGE2)、前列腺素F2α(PGF2α)和6-酮-前列腺素F1α(6-keto-PGF1α)的产生情况以及能评估其合成的孵育条件(时间和细胞数量)。在月经周期的黄体中期(排卵后约8 - 10天),通过手术从未怀孕的猴子体内取出黄体(每次特征分析n = 3)。将黄体组织解离,细胞在37℃下以不同浓度孵育不同时间。在确定孵育条件后,检测了各种外源性因素改变PG产生的潜力。将吲哚美辛、钙离子载体、人绒毛膜促性腺激素(hCG)、雌二醇-17β(E2)、孕酮(P)、睾酮(T)、双氢睾酮(DHT)和1,4,6-雄甾三烯-3,17-二酮(ATD)以递增剂量与黄体细胞一起孵育。通过放射免疫分析法测定培养基中PG和P的浓度。在所有测试的细胞浓度(50,000、100,000、200,000个细胞/管)下,孵育6小时后培养基中的PG均可检测到。PG和P的浓度随细胞数量增加而升高(p < 0.05)。将黄体细胞(50,000个细胞/管)孵育0 - 24小时。孵育前(0小时)培养基中P、PGE2和PGF2α的浓度相对较低,在最初6 - 12小时内呈线性增加(p < 0.05),并在剩余24小时内达到平稳。(摘要截短于250字)

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