Nephro-protective Effect of Clerodendrum infortunatum in Arsenic Induced Sub-acute Toxicity in Albino Rats

Jump To References Section

Authors

  • PG Department of Zoology, Ranchi University, Ranchi – 834001, Jharkhand ,IN
  • Department of Veterinary, Pharmacology and Toxicology, Ranchi Veterinary College, BAU, Ranchi – 834006, Jharkhand ,IN
  • Department of Chemistry, University of Jammu (J&K) – 180006 ,IN
  • PG Department of Zoology, Ranchi University, Ranchi – 834001, Jharkhand ,IN
  • S. S. Memorial College, Ranchi University, Ranchi – 834008, Jharkhand ,IN

DOI:

https://doi.org/10.18311/2019/v26i3&4/24244

Keywords:

Clerodendrum infortunatum, Nephrotoxicity, Phytoconstituents, Rats, Sodium Arsenite, Sub-acute

Abstract

The nephro-protective effect of Clerodendrum infortunatum Linn (C. infortunatum) in arsenic induced sub-acute toxicity (28 days) was evaluated in albino rats. 18 albino rats were divided into 3 groups representing control, sodium arsenite alone and in combination with hydro-methanolic extract of C. infortunatum leaves representing Group I, Group II and Group III respectively. Sodium arsenite (3 mg/kg b.wt.) and C. infortunatum extracts (100 mg/kg b.wt.) were administered orally once daily over a period of 28 days. At the end of treatment period (29th day), rats were sacrificed. The blood samples for hematological parameters and kidney tissues for oxidative stress indices were collected. The kidney weight was also measured. The preliminary phytochemical screening of the above plant was done to know the different phyto-constituents present. Significant reduction were observed in kidney wt., TEC, Hb% and SOD levels where as creatinine, BUN, TLC and MDA levels (P < 0.001) were significantly increased on arsenic exposure. Treatment with extract of C. infortunatum @ 100 mg/kg b.wt for 28 days, significantly reduced the creatinine, BUN, TLC and MDA levels and significantly increased the kidney wt., TEC, Hb% and SOD level (P ≤ 0.001) as compared to arsenic intoxicated group. The major phyto-constituents were present in the leaves i.e. alkaloids, flavonoids, saponins, sterols and terpenes. On the above findings, it can be concluded that treatment with C. infortunatum in sodium arsenite intoxication has significant role in protecting the animals from nephrotoxicity by modulating hemato-biochemical parameters and oxidative stress level.

Downloads

Download data is not yet available.

Published

2020-07-20

How to Cite

Singh, P., Prasad, R., Gupta, V., Kausar, H., & Nehar, S. (2020). Nephro-protective Effect of <i>Clerodendrum infortunatum</i> in Arsenic Induced Sub-acute Toxicity in Albino Rats. Toxicology International, 26(3&amp;4), 129–136. https://doi.org/10.18311/2019/v26i3&4/24244
Received 2019-09-20
Accepted 2019-12-17
Published 2020-07-20

 

References

Singh A, Goel RK, Kaur T. Mechanisms pertaining to arsenic toxicity. Toxicology International. 2011; 18(2): 87–93. PMid: 21976811 PMCid: PMC3183630. https:// doi.org/10.4103/0971-6580.84258

Ginsburg JM. Renal mechanism for excretion and transformation of arsenic in the dog. Am J Physiol.1965;208:837–76. PMid: 14286849. https://doi.org/10.1152/ ajplegacy.1965.208.5.832

Ratnaike RN. Acute and chronic arsenic toxicity.Postgrad Med J. 2003; 79:391–6. PMid: 12897217 PMCid: PMC1742758. https://doi.org/10.1136/pmj.79.933.391

Droge W. Free radicals in the physiological control of cell function. Physiol Rev. 2002; 82:47–95. PMid: 11773609.https://doi.org/10.1152/physrev.00018.2001

Das S, Bhattacharya S, Biswas M, Kar B, Kumar R, Suresh B, Pramanik G, Haldar, PK. Acute and sub-chronic toxicity study of clerodendron infortunatum leaf in adult male albino mice. American-Eurasian Journal of Scientific Research. 2011; 6(4):188–91.

Dymock W. Pharmacographiaindica. M/S periodical experts. Delhi: Vivek Vihar; 1976; 3:79–80.

Panigrahi SS, Prasad R, Ram M, Roy BK, Sharma AK, Singh KK. Clerodendrum infortunatum Linn accelerates wound healing in cutaneous excisional wound model in rats.Journal of Veterinary Pharmacology and Toxicology. 2016; 15(1):62–7.

Sofowara A. Medicinal plants and traditional medicine in Africa. Ibadan, Nigeria: Spectrum Books Ltd; 1993. p. 289.

Trease GE, Evans WC. Textbook of Pharmacognosy Balliere-Tindal: London. 1979. p. 343.

Harborne JB. Phytochemical methods to modern techniques of plant analysis. London: Chapman and Hall; 1984.PMCid: PMC1193218. https://doi.org/10.1007/978-94009-5570-7

Schalm OW, Jain NC, Carroll EJ. Veterinary Hematology, 4th ed. Philadelphia: Lea and Febiger; 1975.

Bowers LD, Wong ET. Kinetic serum creatinine assays.The role of various factors in determining specificity. Clin Chem. 1980; 26(5):551–4. PMid: 7261300. https://doi .org/10.1093/clinchem/26.5.0551

Tiffany-Castiglioni E, Garcia DM, Wu JN, Zmudzki J, Bratton GR. Effects of lead on viability and intracellular metal content of C6 rat glioma cells. J Toxicol Environ Health. 1988; 23:267–79. PMid: 3343700. https://doi .org/10.1080/15287398809531112

Stock J, Dormandy TL. The auto-oxidation of human red cell lipid-induced by hydrogen peroxidation.Br J Haematol. 1971; 20:95–111. PMid: 5540044.https://doi.org/10.1111/j.1365-2141.1971.tb00790.x

Jain, SK. Evidence for membrane lipid peroxidation during the in vivo again of human erythrocytes. Biochem Biophysica Acts. 1988; 937:205–10. https://doi.org/10.1016/0005-2736(88)90242-8

Madesh M, Balasubramanium KA. Microtitre plate assay for superoxide dismutase using MTT reduction by superoxide.Indian J Biochem Biophysics. 1998; 35:184–8.

Snedecor GW, Cochran WG. Statistical methods. 8th ed.Iowa, USA: Iowa State University Press; 1994.

Abbaszadeh G, Srivastava C, Walia S. Insecticidal and antifeedant activities of Clerodone diterpenoids isolated from the Indian bhant tree, Clerodendron infortunatum, against the cotton bollwarm, Helicoverpaarmigera. J Insect Sci.2014; 14(29):1–13. https://doi.org/10.1673/031.014.29

Kapoor LD. Handbook of Ayurvedic Medicinal Plants. 1st ed. New Delhi: CRC Press; 2001; 124–5.

Sannigrahi S, Mazumder UK, Pal D, Parida S. In vitro antioxidant activity of the methanolic extract of Clerodendron infortunatum Linn. OPEM. 2009; 9(20):128–34.https://doi.org/10.3742/OPEM.2009.9.2.128

ATSDR: Toxicological profile for Cadmium: Agency for toxic substance and disease registry. Atlanta GA 2008; 1–454.

Verma RJ, Vasu A, Saiyad AA. Arsenic toxicity in mice and its possible amelioration. J Environ Sci. 2004; 16:447–53.

Gupta R, Flora SJS. Effect of centella asiatica on arsenic induced oxidative stress and metal distribution in rats. J Appl Toxicol. 2006; 26(3):213–22. PMid: 16389662. https:// doi.org/10.1002/jat.1131

Saxena PN, Anand S, Saxena N, Bajaj P. Effect of arsenic trioxide on renal functions and its modulation by Curcuma aromatic leaf extract in albino rats. J Environ Biol. 2009; 30:527–31.

Bhattacharya MA, Lun L. Biochemical effects to toxicity of CCl4 on rosy barabs (Puntius conchonius). Our Nature.2005; 3(1):20–5. https://doi.org/10.3126/on.v3i1.330

Kant V, Kumar D , Prasad R, Gopal A, Pathak NN , Kumar P, Tandan SK. Combined effect of substance P and curcumin on cutaneous wound healing in diabetic rats. Journal of Surgical Research. 2017; 212:130–45. PMid: 28550899.https://doi.org/10.1016/j.jss.2017.01.011

Segue J, Gironella M, Sans M, Granel S, Gil F, Gimeno M, Coronel P, Pique JM, Panes, J. Superoxide dismutase ameliorates TNBS-induced colites by reducing oxidative stress, adhesion molecule expression and leukocyte recruitment into inflamed intestine. J Leukoc Boil. 2004; 76:537–44.PMid: 15197232. https://doi.org/10.1189/jlb.0304196

Sajan R, Singh SP, Varma R, Choudhary GK. Ameliorative efficacy of Piper longum in arsenic induced toxicity in cockerel. J Vet Pharmacol Toxicol. 2009; 8(1-2):41–3.

Rana T, Sarkar S, Mandal TK, Batabyal S.Haematobiochemical profiles of affected cattle at arsenic prone zone in Haringhata block of Nadia District of West Bengal in India. The Internet J Haematol. 2008; 4(2):1642– 57. https://doi.org/10.5580/5a7

Logeswari P, Usha PTA, Kumar DV, Pratha, KSM. Efficacy of Sidarhom bifolla linn. root on cadmium chloride induced haemotological alteration in rats. International Journal of Pharmacy and Technology. 2012; 4(3):4741–8.

Flora SJS, Bhadauria S, Pant SC, Dhaked RK. Arsenic induced blood and brain oxidative stress and its response to some thiol chelators in rats. Life Sci. 2005; 77(18):2324–37.PMid: 15964026. https://doi.org/10.1016/j.lfs.2005.04.016

Gokhale A, Saraf MN. Influence of ethanolic extract of Tephrosia purpurea Linn on the late phase of allergic reaction. Ind J Pharm Sci. 2000; 62(5):356–9.