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1α,25 - 二羟基维生素D3对由12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯和杀鱼菌素B引起的表皮鸟氨酸脱羧酶诱导的抑制作用。

Inhibition by 1 alpha, 25-dihydroxyvitamin D3 of induction of epidermal ornithine decarboxylase caused by 12-O-tetradecanoylphorbol-13-acetate and teleocidin B.

作者信息

Chida K, Hashiba H, Suda T, Kuroki T

出版信息

Cancer Res. 1984 Apr;44(4):1387-91.

PMID:6423272
Abstract

Topical application of 1 alpha, 25-dihydroxyvitamin D3 [1 alpha, 25-(OH)2D3], an active form of vitamin D3, markedly inhibited induction of ornithine decarboxylase caused by 12-O-tetradecanoylphorbol-13-acetate (TPA) and teleocidin B in mouse skin. The degree of inhibition was dependent on the dose and time of application of 1 alpha, 25(OH)2D3. Application of 1 micrograms 1 alpha, 25(OH)2D3 within 30 min before or after treatment with 10 micrograms TPA caused about 72% inhibition of ODC induction at 4 hr. Similar degrees of inhibition were obtained with dose ratios of 1 alpha, 25(OH)2D3 to TPA of 1:3, 1:10, and 1:30. The dose required for 50% inhibition was 0.063 micrograms, or 0.15 nmol, which is about one-half that of retinoic acid, a known inhibitor of induction of ODC activity by TPA. 1 alpha, 25(OH)2D3 had a specific inhibitory effect, in which 100 times higher doses or more of other derivatives of vitamin D3, such as 1 alpha-hydroxyvitamin D3, 25-hydroxyvitamin D3, 24R,25-dihydroxyvitamin D3, and vitamin D3, were required to inhibit ODC induction by TPA. 1 alpha, 25(OH)2D3 did not inhibit epidermal hyperplasia induced by TPA.

摘要

1α,25 - 二羟基维生素D3[1α,25 - (OH)2D3],即维生素D3的一种活性形式,在小鼠皮肤中的局部应用显著抑制了由12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)和teleocidin B引起的鸟氨酸脱羧酶的诱导。抑制程度取决于1α,25(OH)2D3的应用剂量和时间。在10微克TPA处理前或后30分钟内应用1微克1α,25(OH)2D3,在4小时时导致ODC诱导受到约72%的抑制。当1α,25(OH)2D3与TPA的剂量比为1:3、1:10和1:30时,可获得相似程度的抑制。50%抑制所需的剂量为0.063微克,即0.15纳摩尔,这大约是维甲酸(一种已知的TPA诱导ODC活性的抑制剂)的一半。1α,25(OH)2D3具有特异性抑制作用,其中需要高100倍或更多剂量的其他维生素D3衍生物,如1α - 羟基维生素D3、25 - 羟基维生素D3、24R,25 - 二羟基维生素D3和维生素D3,才能抑制TPA诱导的ODC。1α,25(OH)2D3不抑制TPA诱导的表皮增生。

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