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1.
Vopr Pitan ; 88(2): 32-39, 2019.
Artículo en Ruso | MEDLINE | ID: mdl-31233686

RESUMEN

Oxidative stress is a universal mechanism of cellular damage of hepatocytes, leading to a decrease in the detoxification function of the liver, which is especially important during oncogenesis. An early correction of these mechanisms by lipophilic essential nutrients could increase the effectiveness of antitumor treatment and prevent the development and progress of cancer. Aim to study the effect of separate and combined use of ω-3 PUFA and vitamin D3 on the intensity of free radical processes, mitochondrial swelling and cytochrome c content in the liver mitochondrial fraction of the tumor-bearing rats during the intensive growth of the tumor has been studied. Material and methods. Studies were carried out on white outbred female rats weighing 130-150 g, which were divided into 5 groups (each n=12). Guerin's carcinoma was used as a model of malignant neoplasm. Carcinoma transplantation was carried out by subcutaneous injection of 0.5 ml of a 30% suspension of cancer cells into saline in the upper thigh region of the right limb. ω-3 PUFAs (120 mg/kg of body weight, per os) and vitamin D3 (600 IU/kg of body weight, per os) were pre-administered for 28 days before the transplantation of Guerin's carcinoma and after transplantation for the entire period of tumor growth in the body (14 days). Liver mitochondrial fraction was isolated by differential centrifugation. The intensity of lipid peroxidation was judged by using spectrophotometry by the content of primary, secondary, and tertiary products in isopropanol extracts. The rate of formation of the superoxide radical was recorded in a test with nitro-blue tetrazolium, the swelling of mitochondria was assessed by a decrease in the optical density of isolated mitochondria, the content of cytochrome c in the mitochondrial and cytosolic fractions was determined by multi-wavelength visible light spectroscopy. Results and discussion. An increase in the content of primary (diene and triene conjugates), secondary (ketodienes; conjugated trienes; TBA-active products) and terminal (Schiff bases) lipid peroxidation products with a simultaneous increase in the generation of superoxide anion-radical was found in the liver mitochondrial fraction of the tumorbearing rats. With the administration of ω-3 PUFA and vitamin D3, both separately and especially when used together, a decrease in the intensity of free radical processes in liver mitochondrial fraction of tumor-bearing rats has been observed. At the same time, mitochondrial swelling decreased, this prevented the release of cytochrome c from mitochondria into cytosol. Conclusion. The administration of the complex ω-3 PUFA and vitamin D3 reduces the processes of lipid peroxidation in the mitochondrial fraction of the liver of tumor-bearing rats while simultaneously restoring the functional ability of mitochondria.


Asunto(s)
Colecalciferol/farmacología , Ácidos Grasos Omega-3/farmacología , Peroxidación de Lípido/efectos de los fármacos , Mitocondrias Hepáticas/metabolismo , Neoplasias Experimentales/metabolismo , Superóxidos/metabolismo , Animales , Citocromos c/metabolismo , Femenino , Mitocondrias Hepáticas/patología , Neoplasias Experimentales/patología , Ratas
2.
Biomed Khim ; 62(1): 50-5, 2016.
Artículo en Ruso | MEDLINE | ID: mdl-26973187

RESUMEN

The effect of diet supplementation with polyunsaturated fatty acids (PUFAs) used at different ratios of w-6/w-3 was studied on the content of primary (diene conjugates, DC; triene conjugates, TC), secondary (ketodienes, CD; coupled trienes, CT; TBA-active products) and terminal (Schiff bases) lipid peroxidation products (LPO) and generation of superoxide anion-radical in rat heart mitochondrial fraction. It was shown that diet supplementation with high doses of w-6 or w-3 PUFAs increased the content of primary, secondary and terminal LPO in rat heart mitochondrial fraction. Llipid peroxidation was accompanied by the intensification of superoxide anion-radical generation in rat heart mitochondrial fraction. During diet consumption with the PUFAs leading factor affecting the intensity of lipoperoxidation in rat heart mitochondria is fatty acid composition, rather than the level of their saturation.


Asunto(s)
Suplementos Dietéticos , Ácidos Grasos Omega-3/farmacología , Ácidos Grasos Omega-6/farmacología , Peroxidación de Lípido/efectos de los fármacos , Mitocondrias Cardíacas/metabolismo , Animales , Ratas
3.
Ukr Biochem J ; 88(4): 48-56, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-29235764

RESUMEN

The aim of the study was to determine the variations of function in components of monooxygenase system (MOS) of rat Guerin's carcinoma under ω-3 polyunsaturated fatty acids (PUFAs) administration. The activity of Guerin's carcinoma microsomal NADH-cytochrome b5 reductase, the content and the rate of cytochrome b5 oxidation-reduction, the content and the rate of cytochrome Р450 oxidation-reduction have been investigated in rats with tumor under conditions of ω-3 PUFAs administration. ω-3 PUFAs supplementation before and after transplantation of Guerin's carcinoma resulted in the increase of NADH-cytochrome b5 reductase activity and decrease of cytochrome b5 level in the Guerin's carcinoma microsomal fraction in the logarithmic phases of carcinogenesis as compared to the tumor-bearing rats. Increased activity of NADH-cytochrome b5 reductase facilitates higher electron flow in redox-chain of MOS. Under decreased cytochrome b5 levels the electrons are transferred to oxygen, which leads to heightened generation of superoxide (O2•-) in comparison to control. It was shown, that the decrease of cytochrome P450 level in the Guerin's carcinoma microsomal fraction in the logarithmic phases of oncogenesis under ω-3 PUFAs administration may be associated with its transition into an inactive form ­ cytochrome P420. This decrease in cytochrome P450 coincides with increased generation of superoxide by MOS oxygenase chain.


Asunto(s)
Carcinoma/tratamiento farmacológico , Electrones , Ácidos Grasos Omega-3/farmacología , Expresión Génica/efectos de los fármacos , Microsomas/efectos de los fármacos , Sustancias Protectoras/farmacología , Animales , Carcinoma/enzimología , Carcinoma/patología , Sistema Enzimático del Citocromo P-450/genética , Sistema Enzimático del Citocromo P-450/metabolismo , Citocromo-B(5) Reductasa/genética , Citocromo-B(5) Reductasa/metabolismo , Citocromos/genética , Citocromos/metabolismo , Citocromos b5/genética , Citocromos b5/metabolismo , Transporte de Electrón/efectos de los fármacos , Femenino , Miembro Posterior , Inyecciones Subcutáneas , Microsomas/enzimología , Trasplante de Neoplasias , Oxidación-Reducción/efectos de los fármacos , Estrés Oxidativo/efectos de los fármacos , Ratas , Superóxidos/metabolismo
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