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溴隐亭对大鼠自发性垂体肿瘤DNA合成、生长及激素分泌的影响。

Effect of bromocriptine on DNA synthesis, growth and hormone secretion of spontaneous pituitary tumours in the rat.

作者信息

Prysor-Jones R A, Jenkins J S

出版信息

J Endocrinol. 1981 Mar;88(3):463-9. doi: 10.1677/joe.0.0880463.

Abstract

The 'spontaneous' development of pituitary tumours has been studied in the Wistar-Furth strain of rat. In females aged 64--135 weeks the incidence was as high as 69% whereas in males aged 72--116 weeks only 6% developed tumours. Hyperprolactinaemia was invariably associated with these spontaneous pituitary tumours but excessive secretion of growth hormone (GH) was found in one animal only. Bromocriptine inhibited secretion of prolactin and DNA synthesis of the tumours. In a mixed GH- and prolactin-secreting tumour transplanted to a peripheral site, bromocriptine reduced the size of the tumour as well as the secretion of both hormones. Oestradiol reversed the inhibitory action of bromocriptine on prolactin secretion and tumour growth but failed to influence the reduction in GH secretion caused by the drug.

摘要

已在Wistar-Furth品系大鼠中研究了垂体肿瘤的“自发”发展情况。在64至135周龄的雌性大鼠中,发病率高达69%,而在72至116周龄的雄性大鼠中,只有6%发生肿瘤。高催乳素血症总是与这些自发垂体肿瘤相关,但仅在一只动物中发现生长激素(GH)分泌过多。溴隐亭抑制催乳素分泌和肿瘤的DNA合成。在移植到外周部位的混合分泌GH和催乳素的肿瘤中,溴隐亭减小了肿瘤大小并降低了两种激素的分泌。雌二醇逆转了溴隐亭对催乳素分泌和肿瘤生长的抑制作用,但未能影响该药物引起的GH分泌减少。

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