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前列环素对大鼠颅骨钙摄取的刺激作用。

Stimulation of calcium uptake in rat calvaria by prostacyclin.

作者信息

Walenga R W, Bergstrom W

出版信息

Prostaglandins. 1985 Feb;29(2):191-202. doi: 10.1016/0090-6980(85)90201-1.

Abstract

Treatment of newborn rat calvaria discs with a variety of unsaturated fatty acids led to a 50% enhancement of calcium uptake. Arachidonic acid was effective at lower concentrations than cis-vaccenic or oleic acid, while trans-vaccenic acid and saturated fatty acids did not enhance calcium uptake. Cyclooxygenase inhibitors indomethacin and acetylsalicylic acid abolished the enhancement of calcium uptake seen in response to cis-vaccenic acid and inhibited calcium uptake by otherwise untreated bones. Prostacyclin was found to produce up to 2 fold stimulation of calcium uptake with an EC50 of approximately 0.1 microM. No statistically significant stimulation of calcium uptake was seen in response to PGE2 or PGE1 alpha up to 25 microM, while slight stimulation was produced by 6-keto PGE1 alpha but only at concentrations of 10 microM. Prostacyclin production by calvaria was demonstrated and was stimulated over 50% by cis-vaccenic acid. These results suggest that not only is enhanced prostacyclin production responsible for elevation of calcium uptake in response to unsaturated fatty acids, but also that prostacyclin may be an important regulator of bone calcium homeostasis.

摘要

用多种不饱和脂肪酸处理新生大鼠颅骨椎间盘,可使钙摄取增加50%。花生四烯酸在比顺式- vaccenic酸或油酸更低的浓度下就有效,而反式- vaccenic酸和饱和脂肪酸则不会增强钙摄取。环氧化酶抑制剂吲哚美辛和乙酰水杨酸消除了顺式- vaccenic酸引起的钙摄取增强,并抑制了未处理骨骼的钙摄取。发现前列环素可使钙摄取最多增加2倍,其半数有效浓度(EC50)约为0.1微摩尔。在高达25微摩尔的浓度下,未观察到PGE2或PGE1α对钙摄取有统计学意义的刺激作用,而6 -酮- PGE1α仅在10微摩尔的浓度下产生轻微刺激。已证明颅骨可产生前列环素,且顺式- vaccenic酸可使其产生量增加超过50%。这些结果表明,不仅增强的前列环素产生导致了不饱和脂肪酸作用下钙摄取的升高,而且前列环素可能是骨钙稳态的重要调节因子。

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