Author(s): Neeli Parvathi, Iyyam Pillai Subramanian, Sorimuthu Pillai Subramanian

Email(s): subbus2020@yahoo.co.in

DOI: 10.52711/0974-360X.2023.00027   

Address: Neeli Parvathi1, Iyyam Pillai Subramanian2, Sorimuthu Pillai Subramanian1
1Department of Biochemistry, University of Madras, Guindy Campus, Chennai – 600025.
2Associate Professor, PG and Research Department of Chemistry, Pachaiyappa's College, Chennai - 600030.
*Corresponding Author

Published In:   Volume - 16,      Issue - 1,     Year - 2023


ABSTRACT:
Zinc is an essential trace element next to iron in the human system. Its central role in the synthesis, storage, and functional aspects of insulin is well established. Ever since the insulin-mimetic activity of zinc was recognized, several zinc complexes have been synthesized and studied for their antidiabetic and other pharmacological properties. However, its clinical application is narrow due to poor absorption, toxicity associated with prolonged use. Hence, endeavors are being made for the advancement of zinc complexes with various organic ligands of known therapeutic values to avert the toxicity of zinc. Avicularin, a bioactive flavonol originally isolated from the leaves of Polygonum aviculare Linn., is a quercetin derivative in which the a-L-arabinofuranosyl residue is linked at position 3 of quercetin via a glycosidic linkage. It is non-toxic and reported to possess a wide range of pharmacological properties. Though Avicularin is a glycoside of quercetin, it is hydrophilic while quercetin is lipophilic and hence they may differ in absorption rate. In view of the beneficial and pharmacological properties bestowed with Avicularin, recently we have reported the synthesis, spectral characterization and evaluation of antidiabetic properties of a new Zn-Avicularin complex in HFD fed low dose STZ induced experimental type 2 diabetes in rats. In the present study, an attempt has been made to evaluate the antioxidant properties of the Zn-Avicularin complex by analyzing the levels of oxidative stress markers such as lipid peroxides, hydroperoxides and protein carbonyls in the plasma, pancreas, hepatic and renal tissues. The status of enzymatic antioxidants such as SOD, catalase, Glutathione peroxidase as well as non-enzymatic antioxidants such as vitamin C, vitamin E and ceruloplasmin were assayed. Oral administration of the Zn-Avicularin complex at a concentration of 5mg/kg b.w/rat/day for 30 days significantly ameliorates the hyperglycemia-induced oxidative stress in the diabetic groups of rats and the efficacy was comparable with metformin.


Cite this article:
Neeli Parvathi, Iyyam Pillai Subramanian, Sorimuthu Pillai Subramanian. Biochemical Evaluation of Antioxidant properties of A Zn-Avicularin Complex Studied in High Fat Diet Fed- Low Dose Streptozotocin Induced Experimental Type 2 Diabetes in Rats. Research Journal of Pharmacy and Technology 2023; 16(1):145-2. doi: 10.52711/0974-360X.2023.00027

Cite(Electronic):
Neeli Parvathi, Iyyam Pillai Subramanian, Sorimuthu Pillai Subramanian. Biochemical Evaluation of Antioxidant properties of A Zn-Avicularin Complex Studied in High Fat Diet Fed- Low Dose Streptozotocin Induced Experimental Type 2 Diabetes in Rats. Research Journal of Pharmacy and Technology 2023; 16(1):145-2. doi: 10.52711/0974-360X.2023.00027   Available on: https://www.rjptonline.org/AbstractView.aspx?PID=2023-16-1-27


REFERENCES:
1.    Saeedi P. Petersohn I. Salpea P. Malanda B. Karuranga S. Unwin N. Colagiuri S. Guariguata L. Motala AA. Ogurtsova K. Shaw JE. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas. Res. Clin. Pract. 2019; 157-107843. doi.org/10.1016/j.diabres.2019.107843
2.    Karamanou M. Protogerou A. Tsoucalas G. Androutsos G. Poulakou-Rebelakou E. Milestones in the history of diabetes mellitus: The main contributors. World Journal of Diabetes. 2016; 7(1):1. doi.org/10.4239/wjd.v7.i1.1
3.    Fu Z. R Gilbert E. Liu D. Regulation of insulin synthesis and secretion and pancreatic Beta-cell dysfunction in diabetes. Current diabetes reviews. 2013; 9(1):25-53.
4.    Casqueiro J. Casqueiro J. Alves C. Infections in patients with diabetes mellitus: A review of pathogenesis. Indian journal of endocrinology and metabolism. 2012; 16(7): S27-36. doi.org/10.4103/2230-8210.94253
5.    Vijayakumar K. Anand AV. Protective effects of Psidium guajava and its isolated fraction on CCl4 induced oxidative stress. Research Journal of Pharmacy and Technology. 2016; 9(8):1155-60. doi.org/10.5958/0974-360X.2016.00220.1
6.    Choi SW. Ho CK. Antioxidant properties of drugs used in Type 2 diabetes management: could they contribute to, confound or conceal effects of antioxidant therapy. Redox Report. 2018; 23(1):1-24. doi.org/10.1080/13510002.2017.1324381
7.    Osredkar J. Sustar N. Copper and zinc, biological role and significance of copper/zinc imbalance. Journal of Clinical Toxicology.2011; 3(2161): 0495. doi.org/10.4172/2161-0495.S3-001
8.    Babula P. Kohoutková V. Opatrilova R. Dankova I. Masarik M. Kizek R. Pharmaceutical importance of zinc and metallothionein in cell signalling. Chimca Oggi-Chemistry. Today. 2010; 28(3):18-21.
9.    Maret W. Zinc in pancreatic islet biology, insulin sensitivity, and diabetes. Preventive nutrition and food science. 2017; 22(1):1-8. doi.org/10.3746/pnf.2017.22.1.1
10.    Scott DA. Fisher AM. The insulin and the zinc content of normal and diabetic pancreas. The Journal of clinical investigation. 1938; 17(6): 725-8. doi.org/10.1172/JCI101000
11.    Kelleher SL. McCormick NH. Velasquez V. Lopez V. Zinc in specialized secretory tissues: roles in the pancreas, prostate, and mammary gland. Advances in nutrition. 2011; 2(2):101-11. doi.org/10.3945/an.110.000232
12.    Sakurai H. Kojima Y. Yoshikawa Y. Kawabe K. Yasui H. Antidiabetic vanadium (IV) and zinc (II) complexes. Coordination Chemistry Reviews. 2002; 226(1-2):187-98.
13.    Plum LM. Rink L. Haase H. The essential toxin: impact of zinc on human health. International journal of environmental research and public health. 2010; 7(4):1342-65. doi.org/10.3390/ijerph7041342
14.    Skrovanek S. DiGuilio K. Bailey R. Huntington W. Urbas R. Mayilvaganan B. Mercogliano G. Mullin JM. Zinc and gastrointestinal disease. World journal of gastrointestinal pathophysiology. 2014; 5(4):496-513. doi.org/10.4291/wjgp.v5.i4.496
15.    HOU K. The dictionary of genera of seed plants Chinese. ience Press, 1982: 291. Beijing: Sc
16.    Parvathi N. Iyyampillai S. Subramanian S. Design, synthesis and spectral characterization of a new Zinc–Avicularin, a metal flavonol complex and evaluation of its toxicity and antidiabetic efficacy in HFD-Low Dose Streptozotocin Induced Experimental Type 2 Diabetes in Rats. Diabesity. 2020; 6(2):9-18. doi.org/10.15562/diabesity.2020.64
17.    Suman RK. Ray Mohanty I. Borde MK. Maheshwari U. Deshmukh YA. Development of an experimental model of diabetes co-existing with metabolic syndrome in rats. Advances in pharmacological sciences. 2016; 1-11. doi.org/10.1155/2016/9463476.
18.    Nath S. Ghosh SK. Choudhury Y. A murine model of type 2 diabetes mellitus developed using a combination of high fat diet and multiple low doses of streptozotocin treatment mimics the metabolic characteristics of type 2 diabetes mellitus in humans. Journal of pharmacological and toxicological methods. 2017; 84:20-30. doi.org/10.1016/j.vascn.2016.10.007
19.    Vento PJ. Swartz ME. Martin LB. Daniels D. Food intake in laboratory rats provided standard and fenbendazole-supplemented diets. Journal of the American Association for Laboratory Animal Science. 2008; 47(6):46-50.
20.    Jiang ZY. Hunt JV. Wolff SP.  Ferrous ion oxidation in the presence of xylenol orange for detection of lipid hydroperoxide in low density lipoprotein. Analytical biochemistry. 1992; 202(2):384-9. doi.org/10.1016/0003-2697(92)90122-n
21.    Uchida K. Stadtman E. Covalent attachment of 4-hydroxynonenal to glyceraldehyde-3-phosphate dehydrogenase. A possible involvement of intra-and intermolecular cross-linking reaction. Journal of Biological Chemistry. 1993; 268(9):6388-93.
22.    Misra HP. Fridovich I. The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. Journal of Biological chemistry.1972; 247(10):3170-5.
23.    Takahara S. Hamilton HB. Neel JV. Kobara TY. Ogura Y. Nishimura ET. Hypocatalasemia: a new genetic carrier state. The Journal of Clinical Investigation. 1960; 39(4):610-9. doi.org/ 10.1172/JCI104075
24.    Rotruck JT. Pope AL. Ganther HE. Swanson AB. Hafeman DG. Hoekstra W. Selenium: biochemical role as a component of glutathione peroxidase. Science. 1973; 179(4073):588-90. doi.org/10.1126/science.179.4073.588
25.    Habig WH. Pabst MJ. Jakoby WB. Glutathione S-transferases: the first enzymatic step in mercapturic acid formation. Journal of biological Chemistry. 1974; 249(22):7130-9. doi.org/10.1016/S0021-9258(19)42083-8
26.    Omaye ST. Turnbull JD. Sauberlich HE. Selected methods for the determination of ascorbic acid in animal cells, tissues, and fluids. Methods in enzymology. 1979; 62: 3-11. doi.org/ 10.1016/0076-6879(79)62181-x
27.    Desai ID. Vitamin E analysis methods for animal tissues. Methods in enzymology. 1984; 105:138-47. doi.org/ 10.1016/s0076-6879(84)05019-9
28.    Ravin HA. An improved colorimetric enzymatic assay of ceruloplasmin. The Journal of laboratory and clinical medicine. 1961; 58:161–168. doi.org/ 10.1111/j.1651-2227.1960.tb07712.x.
29.    Sedlak J. Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman's reagent. Analytical biochemistry. 1968; 25:192-205. doi.org/ 10.1016/0003-2697(68)90092-4
30.    Marx JL. Oxygen free radicals linked to many diseases; the oxygen free radicals, although made as by-products of normal oxygen-using reactions, nevertheless have a wide potential for causing cell injury. Science. 1987; 235: 529-32. doi.org/ 10.1046/j.1365-2249.2003.02104.x
31.    Nielsen F. Mikkelsen BB. Nielsen JB. Andersen HR. Grandjean P. Plasma malondialdehyde as biomarker for oxidative stress: reference interval and effects of life-style factors. Clinical chemistry. 1997; 43(7):1209-14.
32.    Turko IV. Marcondes S. Murad F. Diabetes-associated nitration of tyrosine and inactivation of succinyl-CoA: 3-oxoacid CoA-transferase. American Journal of Physiology-Heart and Circulatory Physiology. 2001; 281(6):H2289-94. doi.org/10.1152/ajpheart.2001.281.6.H2289
33.    Ponnanikajamideen M. Rajeshkumar S. Annadurai G. In Vivo antidiabetic and in vitro antioxidant and antimicrobial activity of aqueous leaves extract of Chamaecostus cuspidatus. Research Journal of Pharmacy and Technology. 2016; 9(8):1204. doi.org/10.5958/0974-360X.2016.00230.4   
34.    Fatehi D. Moayeri A. Rostamzadeh O. Rostamzadeh A. Kebria MM. Reactive oxygenated species (ROS) in male fertility; source, interaction mechanism and antioxidant therapy. Research Journal of Pharmacy and Technology. 2018; 11(2):791-6.
35.    Biradar KV. Patil CB. Chivde BV. Malipatil MH. Biradar SD. Effect of Superoxide Dismutase Mimetic Tempol on Dexamethasone Induced Insulin Resistance-Role of Oxidative Stress. Research Journal of Pharmacology and Pharmacodynamics. 2011; 3(3):134-7.
36.    Ling PR. Mueller C. Smith RJ. Bistrian BR. Hyperglycemia induced by glucose infusion causes hepatic oxidative stress and systemic inflammation, but not STAT3 or MAP kinase activation in liver in rats. Metabolism. 2003; 52(7):868-74. doi.org/10.1016/s0026-0495(03)00057-x
37.    Vijayakumar K. Anand AV. Protective effects of Psidium guajava and its isolated fraction on CCl4 induced oxidative stress. Research Journal of Pharmacy and Technology. 2016; 9(8):1155-60. doi.org/10.5958/0974-360X.2016.00220.1
38.    Jadhav GB. Saudagar RB. Free radical scavenging and antioxidant activity of Punica granatum Linn. Asian Journal of Research in Pharmaceutical Science. 2014; 4(2):51-4.
39.    Selvam R. Anandhi D. Saravanan D. Revathi K. Antioxidant Properties of Punica grantum Fruit rind extract against liver Hepatocellular Carcinoma studied in HEPG2 Cell Line. Research J. Pharm. and Tech. 2019; 12(10):4719-23. doi.org/10.5958/0974-360X.2019.00813.8
40.    Biradar KV. Patil CB. Chivde BV. Malipatil MH. Biradar SD. Effect of Superoxide Dismutase Mimetic Tempol on Dexamethasone Induced Insulin Resistance-Role of Oxidative Stress. Research Journal of Pharmacology and Pharmacodynamics. 2011; 3(3):134-7.
41.    Davari SA. Talaei SA. Alaei HO. Probiotics treatment improves diabetes-induced impairment of synaptic activity and cognitive function: behavioral and electrophysiological proofs for microbiome–gut–brain axis. Neuroscience. 2013; 240: 287-96. doi.org/10.1016/j.neuroscience.2013.02.055
42.    Wang C. Li S. Shang DJ. Wang XL. You ZL, Li HB. Antihyperglycemic and neuroprotective effects of one novel Cu–Zn SOD mimetic. Bioorganic & medicinal chemistry letters. 2011; 21(14):4320-4. doi.org/10.1016/j.bmcl.2011.05.051
43.    Chelikani P. Fita I. Loewen PC. Diversity of structures and properties among catalases. Cellular and Molecular Life Sciences CMLS. 2004; 61(2):192-208. doi.org/10.1007/s00018-003-3206-5
44.    Takemoto K. Tanaka M. Iwata H. Nishihara R. Ishihara K. Wang DH. Ogino K. Taniuchi K. Masuoka N. Low catalase activity in blood is associated with the diabetes caused by alloxan. Clinica Chimica Acta. 2009; 407(1-2):43-6. doi.org/10.1016/j.cca.2009.06.028
45.    Goth L. Eaton JW. Hereditary catalase deficiencies and increased risk of diabetes. The Lancet. 2000; 356(9244):1820-1. doi.org/ 10.1016/S0140-6736(00)03238-4
46.    Vijayakumar K. Anand AV. Protective effects of Psidium guajava and its isolated fraction on CCl4 induced oxidative stress. Research Journal of Pharmacy and Technology. 2016; 9(8):1155-60. doi.org/10.5958/0974-360X.2016.00220.1
47.    Dash S. Sahoo AC. Mishra B. In vitro and In vivo Antioxidant assessment and Hepatoprotective activity of Aponogeton natans (Linn.) Engl. and Krause on Diclofenac sodium induced Liver Toxicity. Research Journal of Pharmacy and Technology. 2018;11(10):4431-8. doi.org/10.5958/0974-360X.2018.00811.9
48.    Tsai CJ. Hsieh CJ. Tung SC. Kuo MC. Shen FC. Acute blood glucose fluctuations can decrease blood glutathione and adiponectin levels in patients with type 2 diabetes. Diabetes research and clinical practice. 2012; 98(2):257-63. doi.org/10.1016/j.diabres.2012.09.013
49.    Chakravarty S. Rizvi SI. Day and night GSH and MDA levels in healthy adults and effects of different doses of melatonin on these parameters. International journal of cell biology.2011;1-5. doi.org /10.1155/2011/404591
50.    Dinçer Y. Akçay T. Alademir Z. İlkova H. Assessment of DNA base oxidation and glutathione level in patients with type 2 diabetes. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 2002; 505(1-2):75-81. doi.org/10.1016/s0027-5107(02)00143-4

Recomonded Articles:

Research Journal of Pharmacy and Technology (RJPT) is an international, peer-reviewed, multidisciplinary journal.... Read more >>>

RNI: CHHENG00387/33/1/2008-TC                     
DOI: 10.5958/0974-360X 

1.3
2021CiteScore
 
56th percentile
Powered by  Scopus


SCImago Journal & Country Rank

Journal Policies & Information


Recent Articles




Tags


Not Available