The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, Instytucka 3, 05-110 Jabłonna, Poland.
Department of Bromatology, Medical University of Warsaw, Banacha 1, 02-097 Warsaw, Poland.
Nutrients. 2019 Aug 30;11(9):2032. doi: 10.3390/nu11092032.
Breast cancer and cardiovascular diseases (CVD) have shared risk factors and mechanisms of pathogenicity, as proven by increased cardiac risk in breast cancer patients receiving anticancerogenic therapies and in cancer survivors. A growing mammary tumor may cause heart injury in cancer patients who have not yet been treated. This study aimed to evaluate the effect of conjugated linoleic acid (CLA) supplementation of female rats with 7,12-dimethylbenz(a)anthracene (DMBA)-induced cancerogenesis on fatty acids (FAs), conjugated FAs (CFAs), malondialdehyde (MDA), cholesterol and oxysterols content in cardiac tissue. FAs, cholesterol and oxysterols contents were determined by gas chromatography coupled with mass spectrometry, while the contents of CFAs and MDA were determined by high performance liquid chromatography with photodiode detection. Our results indicate that both CLA supplementation and the presence of tumors influence the lipid biomarkers of CVD. A significant interaction of both experimental factors was observed in the content of polyunsaturated FAs (PUFAs), n-6 PUFAs and CFAs. CLA supplementation significantly inhibited PUFA oxidation, as evidenced by the lower content of MDA in rats' hearts, while the cancerous process intensified the oxidation of cholesterol, as confirmed by the elevated levels of 7-ketocholesterol in DMBA-treated rats. These results may significantly expand knowledge about CLA properties in terms of the prevention of co-existing non-communicable diseases.
乳腺癌和心血管疾病(CVD)有共同的风险因素和致病机制,这已被接受抗癌治疗的乳腺癌患者和癌症幸存者的心脏风险增加所证明。未接受治疗的癌症患者中,不断生长的乳腺肿瘤可能导致心脏损伤。本研究旨在评估共轭亚油酸(CLA)对 7,12-二甲基苯并(a)蒽(DMBA)诱导的致癌作用的雌性大鼠脂肪酸(FAs)、共轭脂肪酸(CFAs)、丙二醛(MDA)、胆固醇和氧化固醇含量的影响。通过气相色谱-质谱联用技术测定 FAs、胆固醇和氧化固醇的含量,通过高效液相色谱-光电二极管检测法测定 CFAs 和 MDA 的含量。我们的结果表明,CLA 补充和肿瘤的存在都影响 CVD 的脂质生物标志物。两种实验因素的相互作用在多不饱和脂肪酸(PUFAs)、n-6 PUFAs 和 CFAs 的含量上都有显著表现。CLA 补充显著抑制了 PUFA 的氧化,这可以从大鼠心脏中 MDA 的含量较低得到证明,而癌变过程则加剧了胆固醇的氧化,这可以从 DMBA 处理的大鼠中 7-酮胆固醇水平的升高得到证实。这些结果可能会显著扩展关于 CLA 在预防并存的非传染性疾病方面的性质的知识。