Effect of pineapple, orange and watermelon juices on phosphodiesterase, monoamine oxidase and angiotensin-I converting enzyme activities in rat heart and brain homogenates

被引:6
作者
Ademosun A.O. [1 ]
Oboh G. [1 ]
机构
[1] Functional Foods and Nutraceuticals Unit, Department of Biochemistry, Federal University of Technology, Akure
来源
Oriental Pharmacy and Experimental Medicine | 2017年 / 17卷 / 3期
关键词
Angiotensin; Heart; Orange; Phosphodiesterase; Pineapple; Watermelon;
D O I
10.1007/s13596-017-0279-5
中图分类号
学科分类号
摘要
Fruit juices are commonly consumed in many parts of the world for their nutritional and medicinal benefits. More specifically, Pineapple (Ananas comosus), orange (Citrus sinensis) and watermelon (Citrullus lanatus var. lanatus) juices are used in folklore for the prevention and management of cardiovascular and neurodegenerative diseases, though there is dearth of information on the mechanism for such medicinal benefits. Thetrefore, this study sought to characterize the effect of these commonly consumed fruit juices on phosphodiesterase (PDE), monoamine oxidase (MAO) and angiotensin-I converting enzyme (ACE) activities in rat heart and brain homogenates. The fruits were sourced for and the juices extracted, freeze dried and then reconstituted for the analysis. The abilities of these juices to protect the heart and brain against Fe2+ induced oxidative damage were also investigated in vitro. The results revealed that the juices inhibited PDE, MAO and ACE activities in a concentration-dependent manner in rat heart and brain homogenates with orange having the highest inhibitory ability. The juices also inhibited Fe2+ induced malondialdehyde production in rat heart and brain in a concentration-dependent manner. This study revealed that the inhibition of these enzymes and prevention of oxidative damage could be part of the mechanisms by which these fruits could serve as dietary intervention for the prevention and management of cardiovascular and neurodegenerative diseases. © 2017, Institute of Korean Medicine, Kyung Hee University and Springer Science+Business Media B.V.
引用
收藏
页码:269 / 276
页数:7
相关论文
共 39 条
[21]  
Montezano A.C., Touyz R.M., Molecular mechanisms of hypertension- reactive oxygen species and antioxidants: a basic science update for the clinician, Can J Cardiol, 28, 3, pp. 288-295, (2012)
[22]  
Guide for the care and use of laboratory animals, (2011)
[23]  
Oboh G., Ademosun A.O., Shaddock peels (Citrus maxima) phenolic extracts inhibit a-amylase, a-glucosidase and angiotensin I-converting enzyme activities: a nutraceutical approach to diabetes management, Diabetes Metab Syndr Clin Res Rev, 5, 3, pp. 148-152, (2011)
[24]  
Oboh G., Ademosun A.O., Characterization of the antioxidant properties of phenolic extracts from some citrus peels, J Food Sci Technol, 49, 6, pp. 729-736, (2012)
[25]  
Oboh G., Ademosun A.O., Akinleye M., Omojokun O.S., Boligon A.A., Athayde M.L., Starch composition, glycemic indices, phenolic constituents, and antioxidative and antidiabetic properties of some common tropical fruits, J Ethnic Food, 2, pp. 64-73, (2015)
[26]  
Ohkawa H., Ohishi N., Yagi K., Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction, Anal Biochem, 95, pp. 351-358, (1979)
[27]  
Orallo F., Camina M., Alvarez E., Et al., Implication of cyclic nucleotide phosphodiesterase inhibition in the vasorelaxant activity of the citrus-fruits flavonoid (•})-naringenin, Planta Med, 71, pp. 99-107, (2005)
[28]  
Peluso M.R., Flavonoids attenuate cardiovascular disease, inhibit phosphodiesterase, and modulate lipid homeostasis in adipose tissue and liver, Exp Biol Med (Maywood), 231, 8, pp. 1287-1299, (2006)
[29]  
Perez-Torres S., Cortes R., Tolnay M., Probst A., Palacios J.M., Mengod G., Alterations on phosphodiesterase type 7 and 8 isozyme mRNA expression in Alzheimer’s disease brains examined by in situ hybridization, Exp Neurol, 182, pp. 322-334, (2003)
[30]  
Raasch W., Bartels T., Gieselberg A., Dendorfer A., Dominiak P., Angiotensin I-converting enzyme inhibition increases cardiac catecholamine content and reduces monoamine oxidase activity via an angiotensin type 1 receptor-mediated mechanism, J Pharmacol Exp Ther, 300, pp. 428-434, (2002)