乳腺癌大鼠乳腺和肝脏总atp酶和线粒体atp酶活性的变化

S. Marutyan, Gayane A. Petrosyan, Anna R. Muradyan, Lilit A. Marutyan, S. Marutyan, N. Avtandilyan
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引用次数: 0

摘要

在乳腺癌实验模型中对atp酶进行了初步评价。研究了dmba诱导的乳腺癌大鼠乳腺和肝脏中总atp酶和线粒体atp酶的活性。研究表明,在乳腺癌的发展过程中这些组织的atp酶活性显著增加。同时,在大鼠肝脏中观察到atp酶活性的增加。在用H.alpestre治疗癌症大鼠的情况下,与癌症动物相比,大鼠肝脏匀浆和线粒体中的atp酶活性几乎没有变化。在与化学抑制剂和H.alpestre联合治疗的情况下,使用L-NAME显著降低了atp酶活性,即使与健康动物相比,所获得的值也更低。然而,使用noha后,观察到atp酶活性进一步增加。所获得的结果将允许通过改变能量平衡来评估治疗模型的有效性,并选择进一步的有效剂量,以阐明这些组合模型的影响机制。
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ALTERATION OF TOTAL AND MITOCHONDRIAL ATPASE ACTIVITY IN THE BREAST AND LIVER IN BREAST CANCER-INDUCED RATS
A preliminary evaluation of ATPase was performed in an experimental model of breast cancer. Total and mitochondrial ATPase activities were studied in the breast and liver of rats with DMBA-induced breast cancer. It has been shown that during the development of breast cancer in these tissues there is a significant increase in ATPase activity. At the same time, an increase in ATPase activity is seen in the liver of rats. In the case of treatment cancer rats with H.alpestre, there are almost no changes in ATPase activity in rats' liver homogenate and mitochondria compared to cancer animals. In the case of combined treatment with chemical inhibitors and H.alpestre, ATPase activity is significantly reduced with the use of L-NAME, the values obtained are lower even compared to healthy animals. However, with the use of nor-NOHA, a further increase in ATPase activity is observed. The obtained results will allow evaluation of the effectiveness of the therapeutic model by changing the energy balance, and selecting furthermore effective doses, to clarify the mechanisms of influence of these combination models.
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