首页> 美国卫生研究院文献>Nutrients >Conjugated Linoleic Acid Isomers Affect Profile of Lipid Compounds and Intensity of Their Oxidation in Heart of Rats with Chemically-Induced Mammary Tumors—Preliminary Study
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Conjugated Linoleic Acid Isomers Affect Profile of Lipid Compounds and Intensity of Their Oxidation in Heart of Rats with Chemically-Induced Mammary Tumors—Preliminary Study

机译:共轭亚油酸异构体对化学诱导的乳腺肿瘤大鼠心脏脂质化合物的影响及其氧化强度的初步研究

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摘要

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.
机译:乳腺癌和心血管疾病(CVD)具有共同的危险因素和致病性机制,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证明了这一点。不断增长的乳腺肿瘤可能对尚未接受治疗的癌症患者造成心脏伤害。这项研究旨在评估7,12-二甲基苯并(a)蒽(DMBA)诱导的雌性大鼠共轭亚油酸(CLA)对脂肪酸(FAs),共轭FAs(CFA),丙二醛(MDA)的致癌作用),心脏组织中的胆固醇和氧固醇含量。气相色谱-质谱联用测定FAs,胆固醇和氧固醇含量,高效液相色谱-光电二极管检测法测定CFA和MDA含量。我们的结果表明,补充CLA和肿瘤的存在都会影响CVD的脂质生物标志物。在多不饱和FA(PUFA),n-6 PUFA和CFA的含量中,观察到两个实验因素的显着相互作用。补充CLA可以显着抑制PUFA氧化,这可以通过大鼠心脏中MDA含量的降低来证明,而癌变过程则可以增强胆固醇的氧化,这可以通过DMBA治疗的大鼠中7-酮胆固醇水平的提高来证实。这些结果可能会在预防共存的非传染性疾病方面大大扩展有关CLA性质的知识。

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