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Antioxidant potential of guava leaves extracts and their effects on hyperlipidemia

Eman Manzoor, Ashfa Ghani, Moazzam Rafiq Khan, Muzna Sultana, Aniza Ishaque, Ehtisham Nasir, Muhammad Fahad Latif, Talha Riaz, Asad Sohail

Abstract


The present study was carried out to check out the effect of guava leaves extract on hyperlipidemia. Guava leaves were taken from different orchards of Faisalabad after this mineral and proximate analysis were performed. Three varieties of guava were taken and extract of these three varieties were prepared with different solvents. Among these extracts one of the best variety extract was given to the rats for a period of 30 days. Blood samples were taken at the start, middle and at the end of the study to analysis the level of cholesterol. The maximum effect on the value of glutathione in hypercholestrolemic rats was seen with pink guava leaves extract in S5 the value of glutathione at 0 day was 41.59 ± 1.73 and it increased up to 44.55 ± 2.94 at 30th day. The maximum effect on the value of TBARS in hypercholestrolemic rats was seen with pink guava leaves extract in S5 the value of TBARS at 0 day was 5.58 ± 0.52 and it increased to 6.31 ± 0.87 at 30th day. The maximum effect on the value of urea in hypercholestrolemic rats was seen with pink guava leaves extract in S5 the value of urea at 0 day was 26.45 ± 1.74 and it decreased to 25.54 ± 0.79 at 30th day. Maximum effective results were seen with the ethanolic extract of pink guava leaves the values at 0 day was 0.06 ± 0.02 while it decreased to 0.14 ± 0.03 at 30th day. Least effect on the creatinine was seen with the surahi guava leaves extract in S4 group the value at 0-day was0.96 ± 0.03 while at 30th day it decreases to 0.90 ± 0.03. Mean value of ALT was high in those rats were given pink guava leaves extract as compared to gola extract followed by extract of surahi leaves extract. Mean value of AST was high in those rats were given pink guava leaves extract as compared to gola extract followed by extract of surahi leaves extract. The mean value of DPPH was highest with ethanolic extract of pink guava leaves and its mean value was 66.87 ± 2.67 it was followed by ethanolic extract of gola guava leaves and its value was60.29 ± 3.11 and third best extraction was with ethanolic extract of Surahi leaves and its mean value was 56.75 ± 3.44 on the base of varieties. The mean value of FRAPP was highest with ethanolic extract of pink guava leaves and its mean value was 91.55 ± 2.85 it was followed by ethanolic extract of gola guava leaves and its value was 85.78 ± 1.72and third best extraction was with ethanolic extract of Surahi leaves and its mean value was 80.54 ± 3.05 on the base of varieties. Mean value of TG was minimum in normal rats that was 120.33, value of TG in hyperlipidemic rats was highest that was 164.44, value of TG in rats those were given gola leaves extract its value was 178.15 mg/dl, mean value of TG was 194.85 in rats those were given surahi leaves extract and mean value of TG in rats was 174.85mg/dl in rats those were given extract of pink guava leaves so value of TG was minimum in those rats that were given extract of pink guava leaves so extract of pink guava leaves was best among the gola and surahi. Mean value of cholesterol was minimum in normal rats that was 100.33, value of cholesterol in hyperlipidemic rats was highest that was 218.47mg/dl, value of cholesterol in rats those were given gola leaves extract its value was 202.88 mg/dl, mean value of cholesterol was 232.94 mg/dl in rats those were given surahi leaves extract and mean value of cholesterol in rats was 200.22mg/dl in rats those were given extract of pink guava leaves so value of cholesterol was minimum in those rats that were given extract of pink guava leaves so extract of pink guava leaves was best among the gola and surahi leaves extract. Mean value of LDL was minimum in normal rats that was 47.33, value of LDL in hyperlipidemic rats was highest that was 148.47, value of LDL in rats those were given gola leaves extract its value was 89.88 mg/dl, mean value of LDL was 128.44 mg/dl in rats those were given surahi leaves extract and mean value of LDL in rats was 86.22mg/dl in rats those were given extract of pink guava leaves so value of LDL was minimum in those rats that were given extract of pink guava leaves so extract of pink guava leaves was best among the gola and surahi. The mean value of HDL in rats was 35.52mg/dl in rats those were given extract of pink guava leaves so highest value of HDL was highest in those rats that were given extract of pink guava leaves so extract of pink guava leaves was best among the gola and surahi.

Keywords


Guava, antioxidant, hyperlipidemia, HDL, LDL

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References


Arun, N., & Nalini, N. (2002). Efficacy of turmeric on blood sugar and polyol pathway in diabetic albino rats. Plant Foods for Human Nutrition, 57(1), 41-52.

Asano, K., Kubo, M., Yonemoto, K., Doi, Y., Ninomiya, T., Tanizaki, Y., Iida, M. (2008). Impact of serum total cholesterol on the incidence of gastric cancer in a population‐based prospective study: The Hisayama study. International journal of cancer, 122(4), 909-914.

Chandrika, U., Fernando, K., & Ranaweera, K. (2009). Carotenoid content and in vitro bioaccessibility of lycopene from guava (Psidium guajava) and watermelon (Citrullus lanatus) by high-performance liquid chromatography diode array detection. International journal of food sciences and nutrition, 60(7), 558-566.

Deguchi, Y., & Miyazaki, K. (2010). Anti-hyperglycemic and anti-hyperlipidemic effects of guava leaf extract. Nutrition & metabolism, 7(1), 9.

Donnan, S. K. (1950). The thiobarbituric acid test applied to tissues from rats treated in various ways. Journal of Biological Chemistry, 182(1), 415-420.

Mahendran, T. (2011). Physico-chemical properties and sensory characteristics of dehydrated guava concentrate: effect of drying method and maltodextrin concentration. Tropical Agricultural Research and Extension, 13(2).

Manjunatha, H., & Srinivasan, K. (2007). Hypolipidemic and antioxidant effects of dietary curcumin and capsaicin in induced hypercholesterolemic rats. Lipids, 42(12), 1133.

Mohan, M., Kamble, S., Gadhi, P., & Kasture, S. (2010). Protective effect of Solanum torvum on doxorubicin-induced nephrotoxicity in rats. Food and chemical toxicology, 48(1), 436-440.

Montgomery, D. C., & Woodall, W. H. (2008). An overview of six sigma. International Statistical Review, 76(3), 329-346.

Nwinyi, O. C., Chinedu, S., & Ajani, O. O. (2008). Evaluation of antibacterial activity of Pisidium guajava and Gongronema latifolium. Journal of Medicinal Plants Research, 2(8), 189-192.

Prior, R. L., & Cao, G. (2000). Antioxidant phytochemicals in fruits and vegetables: diet and health implications. HortScience, 35(4), 588-592.

Ravi, K., & Divyashree, P. (2014). Psidium guajava: A review on its potential as an adjunct in treating periodontal disease. Pharmacognosy reviews, 8(16), 96.

Roger, V. L., Go, A. S., Lloyd-Jones, D. M., Adams, R. J., Berry, J. D., Brown, T. M., Ford, E. S. (2011). Heart disease and stroke statistics—2011 update: a report from the American Heart Association. Circulation, 123(4), e18-e209.

Unger, E., Piper, M., & Henry, J. (2001). Clinical diagnosis and management by laboratory methods.

Rafiq, K., Sherajee, S. J., Nishiyama, A., Sufiun, M. A., & Mostofa, M. (2009). Effects of indigenous medicinal plants of Bangladesh on blood glucose level and neuropathic pain in streptozotocin-induced diabetic rats. African Journal of Pharmacy and Pharmacology, 3(12), 636-642.

Rai, P. K., Jaiswal, D., Mehta, S., & Watal, G. (2009). Anti-hyperglycaemic potential of Psidium guajava raw fruit peel. Indian Journal of Medical Research, 129(5), 561.

Rai, P. K., Mehta, S., & Watal, G. (2010). Hypolipidaemic & hepato protective effects of Psidium guajava raw fruit peel in experimental diabetes. Indian J Med Res, 131(820), 820-4.

Reddy, T. P., Manczak, M., Calkins, M. J., Mao, P., Reddy, A. P., Shirendeb, U., & Reddy, P. H. (2011). Toxicity of neurons treated with herbicides and neuroprotection by mitochondria targeted antioxidant SS31. International journal of environmental research and public health, 8(1), 203-221.

Sharma, O. P., & Bhat, T. K. (2009). DPPH antioxidant assay revisited. Food chemistry, 113(4), 1202-1205.

Southon, S. (2000). Increased fruit and vegetable consumption within the EU: potential health benefits. Food Research International, 33 (3-4), 211-217.

Sumino, M., Sekine, T., Ruangrungsi, N., Igarashi, K., & Ikegami, F. (2002). Ardisiphenols and other antioxidant principles from the fruits of Ardisia colorata. Chemical and Pharmaceutical Bulletin, 50(11), 1484-1487.

Tabuchi, Y., Otsuki, M., Kasayama, S., Kosugi, K., Hashimoto, K., Yamamoto, T., & Ohashi, M. (2015). Clinical and endocrinological characteristics of adrenal incidentaloma in Osaka region, Japan. Endocrine journal, EJ15-0404.

Tseng, F. Y., Lai, M. S., Syu, C. Y., & Lin, C. C. (2006). Professional accountability for diabetes care in Taiwan. Diabetes research and clinical practice, 71(2), 192-201.

Zheng, X., Tian, S., Meng, X., & Li, B. (2007). Physiological and biochemical responses in peach fruit to oxalic acid treatment during storage at room temperature. Food Chemistry, 104 (1), 156-162.




DOI: https://doi.org/10.21746/aps.2019.8.5.3



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