beta-carotene has been researched along with acetoacetic-acid* in 3 studies
3 other study(ies) available for beta-carotene and acetoacetic-acid
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[Studies on the antioxidant activities of leaves from Senecio argunensis].
To study antioxidant activities of different extracts of Senecio argunensis.. The antioxidant activities of S. argunensis extracts with acetoacetate, n-Butanol and water were detected by DPPH * free radical-scavenging method and beta-carotene/linoleic acid system.. The acetoacetate, n-Butanol and water extracts from S. argunensis eliminated DPPH * in dose-dependent manner, their EC50 values were 0.0198, 0.0219 and 0.092 mg/ml, respectively. The strength order of the antioxidant activities of the three parts in beta-carotene/linoleic acid system was acetoacetate, n-Butanol and water extracts.. The extracts of the three parts of S. argunensis all have antioxidant activities. Among these extracts, extracts with acetoacetate have the highest antioxidant activity. Topics: Acetoacetates; Antioxidants; Asteraceae; beta Carotene; Biphenyl Compounds; Dose-Response Relationship, Drug; Free Radical Scavengers; Linoleic Acid; Picrates; Plant Extracts; Plant Leaves; Solvents | 2008 |
Effects of oxygen and antioxidants on the mitochondrial Ca-retention capacity.
2-Oxoglutarate-supported rat liver mitochondria were loaded with moderate amounts of calcium and submitted to O2 deprivation and reoxygenation. In the presence of acetoacetate, anaerobic energy production maintained Ca2+ retention by mitochondria during the anoxia period unless the Pi concentration of the incubation solution was raised to 4-6 mM. Acetoacetate prompted Ca2+ release from O2-deprived mitochondria at elevated Pi levels, presumably due to occurrence of a permeability transition of the inner membrane. Providing 3-hydroxybutyrate and malate, together with acetoacetate, was found to delay the permeability transition until O2 was reintroduced, i.e., O2 triggered a paradoxical release of Ca2+ from mitochondria under these conditions. Whether initiated by O2 in the presence of Pi or by Pi under aerobic conditions, Ca2+ release was initially activated and subsequently inhibited or reversed in the presence of alpha-tocopherol (10-90 mumol.g protein-1). Similar effects were exerted by alpha-tocopherol during Pi-induced Ca2+ release from oligomycin-treated mitochondria supported by succinate (+ rotenone). In addition, the permeability transition was delayed by retinol (3-30 mumol.g protein-1) while beta-carotene, ubiquinone, and water-soluble antioxidants, including Trolox C, were ineffective. Other observations suggest that the Ca(2+)-releasing and/or -retaining effects of alpha-tocopherol and retinol may be independent from pro- and/or antioxidant activities. Effects resembling those of alpha-tocopherol were exerted by alpha-tocopherol succinate, which is devoid of antioxidant activity. Our data indicate that the permeability transition of Ca(2+)-loaded liver mitochondria may be triggered by O2, in the presence of ketone bodies, and affected by lipid-soluble antioxidants through mechanisms seemingly unrelated to free-radical generation or scavenging. Topics: Acetoacetates; Anaerobiosis; Animals; Antioxidants; beta Carotene; Calcium; Carotenoids; Chromans; Hypoxia; Kinetics; Mitochondria, Liver; Oligomycins; Oxygen; Oxygen Consumption; Rats; Rats, Sprague-Dawley; Ubiquinone; Vitamin A; Vitamin E | 1993 |
Effects of interferents on the kinetic Jaffé reaction and an enzymatic colorimetric test for serum creatinine concentration determination in cats, cows, dogs and horses.
The effects of acetoacetic acid, acetone, bilirubin, beta-carotene, three cephalospoprin antibiotics, glucose, hemoglobin and lipid on the kinetic Jaffé reaction and an enzymatic reaction for the determination of creatinine concentration were studied in bovine, canine, feline and equine serum. There were no obvious species' differences. The kinetic Jaffé reaction was unaffected by the addition of beta-carotene and hemoglobin. Acetone, cefazolin, cefoxitin, ceftiofur and glucose caused a positive bias while acetoacetic acid, bilirubin, and lipid caused a negative bias when added to the kinetic Jaffé reaction. The enzymatic reaction was unaffected by the addition of acetoacetic acid, acetone, beta-carotene, cefazolin, cefoxitin, glucose and hemoglobin while added lipid, bilirubin and ceftiofur caused a negative bias in the test results. Over all species and interferents, there was no difference in the precision of the two assay methods. In a series of sera from hospitalized patients, the two methods were highly correlated in a linear fashion. The enzymatic creatinine assay deals effectively with most interferents but has a greater cost and shorter shelf-life compared with the kinetic Jaffé reaction. Topics: Acetoacetates; Acetone; Animals; beta Carotene; Bilirubin; Carotenoids; Cats; Cattle; Cephalosporins; Colorimetry; Creatinine; Dogs; Glucose; Hemoglobins; Horses; Kinetics; Lipids | 1991 |