Main Article Content

Abstract

Potassium dichromate is a chemical compound widely used in metallurgy, chrome plating, chemical industry, textile manufacture, wood preservation, photography, photoengraving, refractory, stainless steel industries and cooling systems. Potassium dichromate a compound is the most toxic form of cr (VI) and has been demonstrated to induce nephrotoxicity associated with oxidative stress in humans and animals.


Aim


The present study was aimed to investigate the protective effect of Cardiospermum halicacabum against potassium dichromate induced nephrotoxicity in rats.


Materials and Methods


Rats were divided into four groups of 6 animals each. Group III & group IV received methanolic extract of Cardiospermum halicacabum (100mg/kg, 200mg/kg b.w respectively) consecutively for 5 days. Group 1 (control) received normal saline only. Group II (toxic) received vehicle for 5 days. A single dose of K2cr2o7 (20mg/kg) was administered subcutaneously on 4th day to all the animals except group 1. The protective effects of Cardiospermum halicacabum on K2cr2o7 induced nephrotoxicity was investigated by assaying oxidative stress biomarkers, lipid peroxidation, kidney toxicity markers and by histopathological examination of kidney.


Results and Conclusion


Cardiospermum halicacabum pretreatment prevented toxic effects induced by K2cr2o7 through a protective mechanism that involved reduction of oxidative stress as well as by restoration of histopathological change against  K2cr2o7 administration. In conclusion, the results of the present study showed that the methanolic extract of Cardiospermum halicacabum has protective effect against potassium dichromate induced nephrotoxicity.  

Keywords

K2cr2o7 cardiospermum halicacabum Nephroprotective

Article Details

How to Cite
K. Somasekhar Reddy, A. Sudheer, M. Geethavani, B. Pradeep Kumar, K.V.V. Veerabhadrappa, Y. Padmanabha Reddy, J. Raveendra reddy, & K. Srinivasu. (2021). Protective effect of Cardiospermum halicacabum on potassium dichromate induced nephrotoxicity in rats. International Journal of Research in Pharmacology & Pharmacotherapeutics, 4(4), 411-415. https://doi.org/10.61096/ijrpp.v4.iss4.2015.411-415

References

  1. [1]. Mohamed NE, Saber RA. Effect of aqueous extract of Damsissa (Ambrosia maritima) on the Biochemical changes induced by potassium dichromate in rats. Journal of American science 2011, 7(3), 234-242.
  2. [2]. Hany mehany A, Amira abo-youssef M, Lamiaa ahmed A, El-Shaimaa arafa A, Hekma abd el-latif A. Protective effect of Vitamin E and atorvastatin against potassium dichromate-induced nephrotoxicity in rats. Beni-suef university journal of basic and applied sciences 2013, 2, 96-102.
  3. [3]. Jose pedraza-chaverri, Paola yam-canul, Yolanda chirino I, Dolores Javier Sanchez-gonzalez et al. Protective effects of garlic powder against potassium dichromate-induced oxidative stress and nephrotoxicity. Food and chemical toxicology 2008, 46, 619-627.
  4. [4]. Renato ivan de avila, Meirielle teixeira guerra, Kamilla de almeida souza borges et al. Punica granatum L. protects mice against hexavalent chromium induced genotoxicity. Brazilian journal of pharmaceutical sciences 2013, 49(4), 689-697.
  5. [5]. Barceloux D. Chromium. Clinical toxicology 1999, 37, 173-194.
  6. [6]. Aslam M, Dayal R, Javed K, Parray SA. Nephroprotective effects of methanolic extract of Peucedanum grande against acute renal failure induced by potassium dichromate in rats. International journal of pharmaceutical sciences and drug research 2013, 5(2), 45-49.
  7. [7]. Standevan AM, Wetterhahn KE. Ascorbate is the principal reductant of chromium (VI) in rat liver and kidney ultra W itrates. Carcinogenesis 1991, 12, 1733-1739.
  8. [8]. Liu KJ, Shi X. In-vivo reduction of chromium (VI) and its related free radical generation. Molecular cell biochem 2001, 2222, 41-47.
  9. [9]. Shi XG, Chiu A, Chen CT et al. Reduction of chromium (VI) and its relationship to carcinogenesis. Journal of toxicology environment health 1999, 2, 87-104.
  10. [10]. Sugiyama M. Role of paramagnetic chromium in chromium (VI)-induced damage in cultured mammalian cells. Environment health Perspect 1994, 102, 31-33.
  11. [11]. Bilal S, Mir MR, Parrah JD et al. Rhubarb: the wondrous drug. International journal of pharmacy and biological sciences 2013, 3 (3), 228-233.
  12. [12]. Travacio M, Polo Jm, Llesuy S. Chromium (VI) induces oxidative stress in the mouse brain. Toxicology 2001, 162, 139-148.
  13. [13]. Paola yam canul, Yolanda I et al. Nordihydro guaiaretic acid attenuates potassium dichromate induced oxidative stress and nephrotoxicity. Food and chemical toxicology 2008, 46, 1089-1096.
  14. [14]. Fatima S, Arivarasu NA, Banday AA, Yusufi AN, Mahamood R. Effect of potassium dichromate on renal brush border membrane enzymes and phosphate transport in rats. Human experimental toxicology 2005, 24, 631-638.