Hepatoprotective effect of seabuckthorn leaf-extract in lead acetate-intoxicated Wistar rats

References

• Ahmed, N., 2009. Alloxan diabetes-induced oxidative stress and impairment of oxidative defense system in rat brain: neuroprotective effects of Cichorium intybus. International Journal of Diabetes and Metabolism, 17, 105–109.
   Google Scholar
• Alwaleedi, S.A., 2015. Haemato-biochemical changes induced by lead intoxication in male and female albino mice. International Journal of Recent Scientific Research, 6, 3999–4004.
   Google Scholar
• Anderson, M., 1996. Glutathione In: N.A. Punchard, and F.J. Kelly (eds). Free Radicals, A Practical Approach. New York: Oxford University Press. 213.
   Google Scholar
• Bergmeyer, H.U., 1980. IFCC methods for the measurement of catalytic concentrations of enzymes. Part 3. IFCC method for alanine aminotransferase (L-alanine: 2-Oxoglutarate aminotransferase ec 2.6.1.2). Clinica Chimica Acta, 105, 145–172.
   Web of Science ®Google Scholar
• Bergmeyer, H.U., et al., 1976. Provisional recommendations on IFCC methods for the measurement of catalytic concentrations of enzymes. Part 2. IFCC method for aspartate aminotransferase. Clinica Chimica Acta, 70, 19–29.
   PubMed Web of Science ®Google Scholar
• Bhardwaj, P., et al., 2015. In vitro evaluation of antidiabetic and antioxidant activity of Seabuckthorn (Hippophae rhamnoides L.) leaves. Journal of Medicinal Plants Research, 9, 929–932.
   Google Scholar
• Brraich, O.S., and Kaur, M., 2017. Histopathological alterations in the kidneys of Labeo rohita due to lead toxicity. Journal of Environmental Biology, 38 (2), 257–262.
   Web of Science ®Google Scholar
• Buraimoh, A.A., Bako, I.G., and Ibrahim, F.B., 2011. Hepatoprotective effect of ethanolic leaves extract of Moringa oleifera on the histology of Paracetamol induced liver damage in Wistar Rat. Journal of Animal and Veterinary Advances, 3, 10–13.
   Google Scholar
• Demirezen, D., and Kadiriye, U., 2006. Comparative study of trace elements in certain fish, meat and meat products. Meat Science, 74 (2), 255–260.
   PubMed Web of Science ®Google Scholar
• Duncan, D.B., 1955. Multiple range and multiple F-Tests. Biometrics, 11 (1), 1–42.
   Web of Science ®Google Scholar
• Duruibe, J.O., Ogwuegbu, M.C., and Egwurugw, J.N., 2007. Heavy metal pollution and human biotoxic effects. International Journal of Physical Sciences, 2, 112–118.
   Web of Science ®Google Scholar
• Elayat, W., and Bakheetf, M.S., 2010. Effects of chronic lead toxicity on liver and kidney functions. Journal of Medical Laboratory Science, 1, 29–36.
   Google Scholar
• Flora, G., Gupta, D., and Tiwari, A., 2012. Toxicity of lead: a review with recent updates. Interdisciplinary Toxicology, 5 (2), 47–58.
   PubMedGoogle Scholar
• Geetha, S., et al., 2008. Hepatoprotective effects of Seabuckthorn (Hippophae rhamnoides L.) against carbon tetrachloride induced liver injury in rats. Journal of the Science of Food and Agriculture, 88, 592–1597.
   Web of Science ®Google Scholar
• Geetha, S., et al., 2003. Evaluation of antioxidant activity of leaf extract of Seabuckthorn (Hippophae rhamnoides L.) on chromium induced oxidative stress in albino rats. Journal of Ethnopharmacology, 87 (2–3), 247–251.,
   PubMed Web of Science ®Google Scholar
• Gregus, Z., et al., 1996. Lipoic acid impairs glycine conjugation of benzoic acid and renal excretion of benzoylglycine. Drug Metabolism and Disposition: The Biological Fate of Chemicals, 24 (6), 682–688.
   PubMed Web of Science ®Google Scholar
• Gu, X., and Manautou, J.E., 2012. Molecular mechanisms underlying chemical liver injury. Expert Reviews in Molecular Medicine, 14, e4.
   PubMed Web of Science ®Google Scholar
• Harbison, R. D., 1998. Lead. In: Hamilton & Hardy’s Industrial Toxicology, 5th ed., Philadelphia: Mosby. 70–76.
   Google Scholar
• Ibrahim, N.M., et al., 2012. Effect of lead acetate toxicity on experimental male albino rat. Asian Pacific Journal of Tropical Biomedicine, 2 (1), 41–46.
   PubMedGoogle Scholar
• Jawhar, L., et al., 2017. Berberis vulgaris effects on oxidative stress and liver injury in lead-intoxicated mice. Journal of Complementary and Integrative Medicine, 14, 1–7.
   Google Scholar
• Kanchana, N., and Sadiq, A.M., 2011. Hepatoprotective effect of Plumbago Zeylanica on paracetamol induced liver toxicity in rats. International Journal of Pharmacy and Pharmaceutical Sciences., 3, 151–154.
   Google Scholar
• Kansal, L., et al., 2011. Protective role of coriandrum sativum (coriander) extracts against lead nitrate induced oxidative stress and tissue damage in the liver and kidney in male mice. International Journal of Applied Biology and Pharmaceutical Technology, 2, 65–83.
   Google Scholar
• Khajuria, P., et al., 2018. Hepatoprotective effect of seabuckthorn leaf extract in streptozotocin induced diabetes mellitus in Wistar rats. Indian Journal of Animal Research, 52, 1745–1750.
   Web of Science ®Google Scholar
• Kumar, Y.M.S., et al., 2011. Subcritical water extraction of antioxidant compounds from Seabuckthorn (Hippophae Rhamnoides) leaves for the comparative evaluation of antioxidant activity. Food Chemistry, 127 (3), 1309–1316.,
   PubMed Web of Science ®Google Scholar
• Lamidi, I.Y., and Akefe, I.O., 2017. Mitigate effects of antioxidants in Lead Toxicity. Basic & Clinical Pharmacology & Toxicology, 1, 1–9.
   Google Scholar
• Li, T.S.C., and Schroeder, W.R., 1996. Seabuckthorn (Hippophae rhamnoides): a multipurpose plant. HortTechnology, 6 (4), 370–380.
   Google Scholar
• Maheshwari, D.T., et al., 2011. Antioxidant and hepatoprotective activities of phenolic rich fraction of Seabuckthorn (Hippophae rhamnoides L.) leaves. Food and Chemical Toxicology, 49 (9), 2422–2428.,
   PubMed Web of Science ®Google Scholar
• Masella, R., et al., 2005. Novel mechanisms of natural antioxidant compounds in biological systems: involvement of glutathione and glutathione-related enzymes. The Journal of Nutritional Biochemistry, 16 (10), 577–586.
   PubMed Web of Science ®Google Scholar
• Mehrotra, V., Saxena, V.L., and Saxena, A.K., 2008. Impact of different doses of lead on internal organs of quails. Journal of Environmental Biology., 29, 147–149.
   PubMed Web of Science ®Google Scholar
• Nariya, A., et al., 2018. Ameliorative effects of curcumin against lead induced toxicity in human peripheral blood lymphocytes culture. Drug and Chemical Toxicology, 41 (1), 1–8.
   PubMed Web of Science ®Google Scholar
• Omotoso, B.R., et al., 2015. Lead-induced damage on hepatocytes and hepatic reticular fibres in rats; protective role of aqueous extract of Moringa oleifera leaves (Lam). Journal of Biosciences and Medicines, 03 (05), 27–35.
   Google Scholar
• Roy, A.V., Brower, M.E., and Hayden, J.E., 1971. Sodium thymolphthalein monophosphate: a new acid phosphatase substrate with greater specificity for the prostatic enzyme in serum. Clinical Chemistry, 17 (11), 1093–1102.
   PubMed Web of Science ®Google Scholar
• Saggu, S., et al., 2007. Adaptogenic and safety evaluation of Seabuckthorn (Hippophae rhamnoides) leaf extract: a dose dependent study. Food and Chemical Toxicology: An International Journal Published for the British Industrial Biological Research Association, 45 (4), 609–617.,
   PubMed Web of Science ®Google Scholar
• Sagrawat, H., Mann, A.S., and Kharya, M.D., 2006. Pharmacological potential of Eugenia jambolana: a review. Pharmacognosy Magazine., 2, 96–105.
   Google Scholar
• Samir, D., et al., 2017. Protective effects of Aristolochia longa and Aquilaria malaccensis against lead induced acute liver injury in rats. Journal of Acute Disease, 6 (5), 193–197.
   Web of Science ®Google Scholar
• Shah, F.C., and Jain, N.K., 2016. Ameliorative action of synthetic and herbal antioxidants on lead induced hepatotoxicity: an in vitro study. Asian Journal of Pharmaceutical and Clinical Research., 9, 364–370.
   Google Scholar
• Sharma, S.K., Singh, L., and Singh, S., 2013. A review on medicinal plants having antioxidant potential. Indian Journal of Research in Pharmacy and Biotechnology, 3, 404–409.
   Google Scholar
• Shawky, N.M., et al., 2014. Levocetirizine ameliorates high fructose diet-induced insulin resistance, vascular dysfunction and hepatic steatosis in rats. European Journal of Pharmacology, 740, 353–363.
   PubMed Web of Science ®Google Scholar
• Simagol, G., et al., 2017. Beneficial effects of garlic on learning and memory deficits and brain tissue damages induced by lead exposure during juvenile rat growth is comparable to the effect of ascorbic acid. Drug and Chemical Toxicology., 40, 206–214.
   PubMed Web of Science ®Google Scholar
• Snedecor, G. W., and Cochran, W. G., 1994. Statistical methods. 8th ed. New Delhi: East West Press Private Limited.
   Google Scholar
• Suganthi, V., Gowri, S., and Gurusamy, K., 2013. Hepatoprotective activity of Cayratia carnosa on liver damage caused by lead acetate in rats. Journal of Natural Product and Plant Resources, 3, 76–79.
   Google Scholar
• Suradkar, S.G., et al., 2009. Hemato biochemical Alterations induced by lead acetate toxicity in Wistar rats. Veterinary World, 11, 429–439.
   Google Scholar
• Suryakumar, G., and Gupta, A., 2011. Medicinal and therapeutic potential of Sea buckthorn (Hippophae rhamnoides L.). Journal of Ethnopharmacology, 138 (2), 268–278.
   PubMed Web of Science ®Google Scholar
• Townsend, D.M., Tew, K.D., and Tapiero, H., 2003. The importance of glutathione in human disease. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie, 57 (3–4), 145–155.
   PubMed Web of Science ®Google Scholar
• Upadhyay, N.K., Kumar, M.S., and Gupta, A., 2010. Antioxidant, cytoprotective and antibacterial effects of Sea buckthorn (Hippophae rhamnoides L.) leaves. Food and Chemical Toxicology : An International Journal Published for the British Industrial Biological Research Association, 48 (12), 3443–3448.
   PubMed Web of Science ®Google Scholar
• Velaga, M.K., et al., 2014. Hydroalcoholic seed extract of Coriandrum sativum (Coriander) alleviates lead-induced oxidative stress in different regions of rat brain. Biological Trace Element Research, 159 (1–3), 351–363.
   PubMed Web of Science ®Google Scholar
• Virk, P., et al. 2017. Characterization of nanorosemary and encapsulated rosemary nanoparticles and their effect on lead induced toxicity in Wistar rats. Journal of Environmental Biology, 38 (6), 1333–1340.
   Web of Science ®Google Scholar
• Wilkinson, J.H., Boutwell, J.H., and Winsten, S., 1969. Evaluation of a new system for the kinetic measurement of serum alkaline phosphatase. Clinical Chemistry, 15 (6), 487–495.
   PubMed Web of Science ®Google Scholar
• Witte, V.C., Krause, G.F., and Bailey, M.E., 1970. A new extraction method for determining 2-thiobarbituric acid value of pork and beef during storage. Journal of Food Science, 35 (5), 582–585.
   Google Scholar
• Zargar, R., et al., 2016. Protective and ameliorative effect of sea buckthorn leaf extract supplementation on lead induced hemato-biochemical alterations in Wistar rats. Veterinary World, 9 (9), 929–934.,
   PubMed Web of Science ®Google Scholar
• Zhang, W., et al., 2010. Hypoglycemic effect of aqueous extract of Seabuckthorn (Hippophae rhamnoides L.) seed residues in Streptozotocin-induced diabetic rats. Phytotherapy Research, 24 (2), 228–232.
   PubMed Web of Science ®Google Scholar