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Hormone and drug effects on growth of DMBA mammary tumours and plasma prolactin levels in adreno-ovariectomized rats.

机译:激素和药物对肾上腺切除卵巢大鼠DMBA乳腺肿瘤生长和血浆催乳素水平的影响。

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摘要

The effects of hormone and drug treatments on plasma prolactin (PRL) levels and mammary tumour growth were investigated in rats bearing continuously growing DMBA-induced mammary tumours that responded to bilateral adreno-ovariectomy (Ax + Ox), Oestrogen (E2) administration increased both plasma PRL and tumour growth, but was unable to sustain tumour growth when the PRL level was reduced by concurrent injection of ergocornine (Eg). Perphenazine (Pz) produced a dose-related increase in plasma PRL, but stimulation of tumour growth in the absence of E2 required a minimal level of plasma PRL induced by Pz (0.15 mg/100 g body wt/day or more). Progesterone (P) (3 mg/day) alone, although without effect on PRL levels, maintained static tumour growth (i.e. it had a slight stimulatory effect) irrespective of the duration of treatment. The increase in plasma PRL levels above the basal values in the Ax + Ox controls following injections of combined P + Pz (0.1 mg/100 g/day) was sufficient to sustain static tumour growth, but not to reactivate growth. Enhancement of both plasma PRL and tumour growth did not occur until P and higher doses of Pz (0.3 mg/100 g/day) were injected jointly; this treatment, however, while unable to stimulate continuous tumour growth, was able to maintain static growth when plasma PRL was reduced by concurrent injections of P + Pz + Eg. From these findings it is postulated that the mechanism of action whereby P maintains static tumour growth is different from that of PRL and independent of circulating PRL levels.
机译:研究了荷尔蒙和药物治疗对血浆中催乳素(PRL)水平和乳腺肿瘤生长的影响,该大鼠具有持续生长的DMBA诱发的乳腺肿瘤,该乳腺肿瘤对双侧肾上腺卵巢切除术(Ax + Ox)有反应,雌激素(E2)的使用均增加血浆PRL和肿瘤生长,但是当同时注射麦角go碱(Eg)降低PRL水平时,则无法维持肿瘤生长。奋乃静(Pz)在血浆PRL中产生剂量相关的增加,但是在没有E2的情况下刺激肿瘤生长需要Pz诱导的血浆PRL达到最低水平(0.15 mg / 100 g体重/天或更多)。单独的孕酮(P)(3 mg /天),尽管对PRL水平没有影响,但无论治疗持续时间如何,都可以维持静态肿瘤生长(即,具有轻微的刺激作用)。注射P + Pz(0.1 mg / 100 g /天)后,血浆PRL水平升高至高于Ax + Ox对照的基础值,足以维持静态肿瘤生长,但不能重新激活生长。直到同时注射P和更高剂量的Pz(0.3 mg / 100 g / day)时,血浆PRL和肿瘤生长都没有增强。然而,这种治疗虽然不能刺激连续的肿瘤生长,但是当同时注射P + Pz + Eg降低血浆PRL时能够维持静态生长。根据这些发现,推测P维持静态肿瘤生长的作用机理与PRL不同,并且与循环PRL水平无关。

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