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1.
Lipids Health Dis ; 18(1): 53, 2019 Feb 14.
Artículo en Inglés | MEDLINE | ID: mdl-30764880

RESUMEN

BACKGROUND: Supplemented fatty acids can incorporate into cardiolipin (CL) and affect its remodeling. The change in CL species may alter the mitochondrial membrane composition, potentially disturbing the mitochondrial structure and function during inflammation. METHOD: To investigate the effect of the unsaturation of fatty acids on CL, we supplemented macrophage-like RAW264.7 cells with 18-carbon unsaturated fatty acids including oleic acid (OA, 18:1), linoleic acid (LA, 18:2), α-linolenic acid (ALA, 18:3), γ-linolenic acid (GLA, 18:3), and stearidonic acid (SDA, 18:4). Mitochondrial changes in CL were measured through mass spectrometry. RESULT: Our data indicated that OA(18:1) was the most efficient fatty acid that incorporated into CL, forming symmetrical CL without fatty acid elongation and desaturation. In addition, LA(18:2) and ALA(18:3) were further elongated before incorporation, significantly increasing the number of double bonds and the chain length of CL. GLA and SDA were not optimal substrates for remodeling enzymes. The findings of RT-qPCR experiments revealed that none of these changes in CL occurred through the regulation of CL remodeling- or synthesis-related genes. The fatty acid desaturase and transportation genes-Fads2 and Cpt1a, respectively-were differentially regulated by the supplementation of five unsaturated 18-carbon fatty acids. CONCLUSIONS: The process of fatty acid incorporation to CL was regulated by the fatty acid desaturation and transportation into mitochondria in macrophage. The double bonds of fatty acids significantly affect the incorporation process and preference. Intact OA(18:1) was incorporated to CL; LA(18:2) and ALA(18:3) were desaturated and elongated to long chain fatty acid before the incorporation; GLA(18:3) and SDA(18:4) were unfavorable for the CL incorporation.


Asunto(s)
Cardiolipinas/biosíntesis , Ácidos Grasos Omega-3/farmacología , Ácido Linoleico/farmacología , Membranas Mitocondriales/efectos de los fármacos , Ácido Oléico/farmacología , Ácido alfa-Linolénico/farmacología , Ácido gammalinolénico/farmacología , Animales , Transporte Biológico , Carnitina O-Palmitoiltransferasa/genética , Carnitina O-Palmitoiltransferasa/metabolismo , Ácido Graso Desaturasas/genética , Ácido Graso Desaturasas/metabolismo , Ácidos Grasos Omega-3/química , Ácidos Grasos Omega-3/metabolismo , Perfilación de la Expresión Génica , Regulación de la Expresión Génica , Ácido Linoleico/química , Ácido Linoleico/metabolismo , Ratones , Mitocondrias/química , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Membranas Mitocondriales/química , Membranas Mitocondriales/metabolismo , Ácido Oléico/química , Ácido Oléico/metabolismo , Células RAW 264.7 , Relación Estructura-Actividad , Ácido alfa-Linolénico/química , Ácido alfa-Linolénico/metabolismo , Ácido gammalinolénico/química , Ácido gammalinolénico/metabolismo
2.
Artículo en Inglés | WPRIM | ID: wpr-344977

RESUMEN

<p><b>OBJECTIVE</b>To study the effects and possible mechanisms of effective composite of Naodesheng (NDS) on permanent cerebral ischemia-induced injury in rats.</p><p><b>METHODS</b>Male Sprague-Dawley rats: with middle cerebral artery occlusion (MCAO) were established with the modified suture method, and they were randomly divided into the following groups: the sham-operated group, the model group, the Nimodipine group (0.012 g/kg), the NDS group (1.075 g/kg), the total extracts group (0.23 g/kg), the high-dose NEC group (0.07 g/kg), the middle-dose NEC group (0.02 g/kg), and the low-dose NEC group (0.007 g/kg). The aforesaid medicines were administered at the 2nd, 4th, and 24th h after focal cerebral ischemia, and the infarction size and water content in the brain were evaluated at the 26th h after MCAO. Then, after oral administration once daily for 7 successive days, the changes in the degree of neurological deficit, oxidative stress, and apoptosis were measured on the 7th day.</p><p><b>RESULTS</b>NEC could significantly reduce the infarction size after focal cerebral ischemia, and slightly relieve water content in the brain, significantly alleviate neurological function impairment, increase the levels of superoxide dismutase (SOD) and adenosine triphosphate enzyme (ATPase) activity, and decrease the content of malondialdehyde (MDA). NEC could also extenuate Bax and caspase-3 expression in the hippocampus tissue of the ischemic region. As compared with the three NEC treated groups, the high-dose NEC showed better efficacy.</p><p><b>CONCLUSIONS</b>NEC could significantly reduce brain injury induced by ischemia;: its mechanism was closely associated with hindering oxidative stress and apoptosis. The effective composite-guided methodology is a feasible tool to improve the neuro-protective properties of the Chinese medicine guided prescription NDS against focal cerebral ischemia in rats.</p>


Asunto(s)
Animales , Masculino , Ratas , Adenosina Trifosfatasas , Metabolismo , Western Blotting , Isquemia Encefálica , Caspasa 3 , Metabolismo , Medicamentos Herbarios Chinos , Farmacología , Hipocampo , Metabolismo , Patología , Malondialdehído , Metabolismo , Fármacos Neuroprotectores , Farmacología , Células Piramidales , Ratas Sprague-Dawley , Superóxido Dismutasa , Metabolismo , Proteína X Asociada a bcl-2 , Metabolismo
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