Protective Role of Pongamia Pinnata Leaf Extract on Tissue Antioxidant Status and Lipid Peroxidation in Ammonium Chloride-Induced Hyperammonemic Rats

REFERENCES

• Ahmad G., Yadav P. P., Maurya R. Furanoflavonoid glycosides from Pongamia pinnata fruits. Phytochemistry 2004; 65: 921–924
   PubMed Web of Science ®Google Scholar
• Baynes J. W. Reactive oxygen in the aetiology and complications of diabetes. In: Ioannides C. Drug, Diet and Disease, PR Flatt, eds. Mechanistic Approach to Diabetes. Hertfordshive: Ellis Horwood Limited. 1995; volume 2: 230–231
   Google Scholar
• Bruce A., Freeman D., James C. Biology of disease-free radicals and tissue injury. Lab. Invest. 1982; 47: 412–426
   PubMed Web of Science ®Google Scholar
• Chance B., Greenstein D. S., Roughton R. J. W. The mechanism of catalase action—steady state analysis. Arch. Biochem. Biophys. 1952; 37: 301–339
   PubMed Web of Science ®Google Scholar
• Chopra R. N. Indigenous Drugs of India. Academic Publishers, Calcutta, 388 1933; 388
   Google Scholar
• Dakshayani K. B., Velvizhi S., Subramanian P. Effects of ornithine alpha ketoglutarate on circulatory antioxidants and lipid peroxidation products in ammonium acetate treated rats. Ann. Nutr. Metab. 2002a; 46: 93–96
   PubMed Web of Science ®Google Scholar
• Dakshayani K. B., Velvizhi S., Subramanian P. Ornithine alpha ketoglutarate modulates the levels of antioxidants and lipid peroxidation products in ammonium acetate treated rats. Ind. J. Biochem. Biophys. 2002b; 36: 422–424
   Google Scholar
• Devipriya S., Shyamaladevi C. S. Protective effect of quercetin in cisplastin induced cell injury in the rat kidney. Ind. J. Pharmacol. 1999; 31: 422
   Google Scholar
• Elman G. L. Tissue sulfyhdryl groups. Arch. Biochem. Biophys. 1959; 82: 70–77
   PubMed Web of Science ®Google Scholar
• Essa M. M., Subramanian P., Suthakar G., Manivasagam T., Dakshayani K. B. Protective influence of Pongamia pinnata (Karanja) on blood ammonia and urea levels in ammonium chloride-induced hyperammonemia. J. Appl. Biomed. 2005; 3: 133–138
   Google Scholar
• Halliwell B., Gutteridge J. M. C. Free radicals and toxicology. In:. Free Radicals in Biology and Medicine. Clarendon Press, Oxford 1985; 1–27
   Google Scholar
• Halliwell B., Gutterridge J. M. C. Lipid peroxidation, oxygen radicals, cell damage and antioxidant therapy. Lancet 1994; 1: 1396–1397
   Google Scholar
• Hilgier W., Albrecht J., Lisy V., Stastny F. The effect of acute and repeated hyperammonemia on gamma-glutamyl transpeptidase in homogenates and capillaries of various rat brain regions. Mol. Chem. Neuropathol. 1994; 13: 47–56
   Google Scholar
• Jiang Z. Y., Hunt J. V., Wolff S. P. Detection of lipid hydroperoxides using the Fox reagent. Ana. Biochem. 1992; 202: 384–389
   PubMed Web of Science ®Google Scholar
• Kakkar P., Das B., Viswanathan P. N. A modified spectrophotometric assay of superoxide dismutase. Ind. J. Biochem. Biophys. 1984; 22: 130–132
   Google Scholar
• Kinalski M., Sledziewski A., Telejko B., Zarzycki W., Kinalska T. Lipid peroxidation and scavenging enzyme activity in streptozotocin induced diabetes. Acta. Diabeto. 2000; 37: 179–183
   PubMed Web of Science ®Google Scholar
• Kirtikar K. R., Basu B. D. Indian medicinal plants. International Book Distributors2nd ed. Dehraduneindia 1995; vol 1
   Google Scholar
• Klein R. A. The detection of oxidation in liposome preparation. Biochim. Biophys. Acta. 1979; 210: 486–489
   Google Scholar
• Kosenko E., Kaminsky A., Valencia M., Lee L., Hermenegildo C., Felipo V. Superoxide production and antioxidant enzymes in ammonia intoxication in rats. Free Radic. Res. 1997; 27: 637–644
   PubMed Web of Science ®Google Scholar
• Kosenko E., Kaminsky Y., Lopata O., Muravyov N., Kaminsky A., Hermenegildo C., Stavroskaya I. G., Felipo V. Nitroarginine, an inhibitor of nitric oxide synthase, prevents changes in superoxide radical and antioxidant enzymes induced by ammonia intoxication. Metab. Brain. Dis. 1998; 13: 29–41
   PubMed Web of Science ®Google Scholar
• Kosenko E., Kaminsky Y., Stavroskaya I. G., Felipo V. Alteration of mitochondrial calcium homeostasis by ammonia-reduced activation of NMDA receptors in rat brain in vivo. Brain Res. 2000; 880: 139–146
   PubMed Web of Science ®Google Scholar
• Krishnamurthi A. The Wealth of India. Publication and Information Directorate, CSIR, New DelhiIndia 1969; vol VIII
   Google Scholar
• Lena P. J., Subramanian P. Evaluation of the antiperoxidative effects of melatonin in ammonium acetate-treated Wistar rats. Pol. J. Pharmacol. 2003; 55: 1031–1036
   PubMedGoogle Scholar
• Lena P. J., Subramanian P. Effects of melatonin on the levels of antioxidants and lipid peroxidation products in rats treated with ammonium acetate. Pharmazie 2004; 59: 636–639
   PubMed Web of Science ®Google Scholar
• Majeed K. I. Hyperammonemia is associated with an increase in inhibitory neurotransmission as a consequence of two factors. E. Med. J. 2005; 2: 2–15
   Google Scholar
• Mathias R. S., Kostiner D., Packman S. Hyperammonemia in urea cycle disorders: role of the nephrologist. Am. J. Kidney. Dis. 2001; 37: 1069–1080
   PubMed Web of Science ®Google Scholar
• Mccord J. M., Keele B. B., Fridovich I. An enzyme based theory of obligate anaerobiosis, the physiological functions of superoxide dismutase. Proc. Natl. Acad. Sci. USA 1976; 68: 1024–7
   Web of Science ®Google Scholar
• Monfort P., Felipo V. Long-term potentiation in hippocampus involves sequential activation of soluble guanylate cyclase, cGMP-dependent protein kinase and cGMP-degrading phosphodiesterase, alterations in hyperammonemia. BMC Pharmacol. 2005; 5(Suppl 1)P66
   Google Scholar
• Murthy C. R., Rama Rao K. V., Bai G., Norenburg M. D. Ammonia induced production of free radicals in primary cultures of rat astrocytes. J. Neurosci. Res. 2001; 66: 282–288
   PubMed Web of Science ®Google Scholar
• Murthy P. B. R., Seshadri T. R. Chemical examination of the flowers of Pongamia glabra and a note on the glycosidic components of Bueta frondosa flowers. Proc. Ind. Acad. Sci. 1944; 20A: 279–291
   Google Scholar
• Nadkarni K. M. Indian Materia Medica. Popular Book Depot, BombayIndia 1954; vol 1: 1001
   Google Scholar
• Niehaus W. G., Samuelson B. Formation of malondialdehyde from phospholipid arachidonate during microsomal lipid peroxidation. Eur. J. Biochem. 1968; 6: 126–130
   PubMedGoogle Scholar
• Pathak V. P., Saini T. R., Khanna R. N. Glabrachalcone a chromenochalcone from Pongamia glabra seeds. Phytochemistry 1983; 22: 1303–1304
   Web of Science ®Google Scholar
• Prabha T., Dora Babu M., Priyambada S., Agrawal V. K., Goel R. K. Evaluation of Pongamia pinnata root extract on gastric ulcers and mucosal offensive and defensive factors in rats. Ind. J. Exp. Biol. 2003; 41: 304–310
   PubMedGoogle Scholar
• Rangasami S., Rao J. V., Seshadri T. R. Kanugin, a crystalline compound of the roots of Pongamia glabra. Proc. Ind. Acad. Sci. 1942; 16A: 319–322
   Google Scholar
• Rice-Evans C. A., Miller N. J., Paganga G. Structure-antioxidant activity relationships of flavonoids and phenolic acids. Free Radic. Biol. Med. 1996; 20: 933–956
   PubMed Web of Science ®Google Scholar
• Rodrigo R., Montoliu C., Chatauret N., Butterworth R., Behrends S., Olmo J. A. D., Serra M. A., Rodrigo J. M., Erceg S., Felipo V. Alterations in soluble guanylate cyclase content and modulation by nitric oxide in liver disease. Neurochem. Int. 2004; 45: 947–953
   PubMed Web of Science ®Google Scholar
• Rotruck J. T., Pope A. L., Ganther H. E., Swanson A. B., Hafeman D. G., Hoekstra W. G. Selenium: biochemical roles as components of glutathione peroxidase. Science 1973; 179: 588–590
   PubMed Web of Science ®Google Scholar
• Saez R., Liansola M., Felipo V. Chronic exposure to ammonia alters pathways modulating phosphorylation of microtubule associated protein 2 in cerebellar neurons in culture. J. Neurochem. 1999; 73: 2555–2562
   PubMed Web of Science ®Google Scholar
• Satyavati G. V., Gupta A. K., Neeraj T. Medicinal plants of India (ICMR, New Delhi). 1987; 2: 490
   Google Scholar
• Schliess F., Gorg B., Fischer R., Desjardins P., Bidmon H. J., Herrmann A., Butterworth R. F., Zilles K., Haussinger D. Ammonia induces MK-801-sensitive nitration and phosphorylation of protein tyrosine and residues in rat astrocytes. FASEB J. 2002; 16: 739–741
   PubMed Web of Science ®Google Scholar
• Searle A. J., Wilson R. Glutathione perioxide effect of superoxide, hydroxyl and bromine free radicals on enzyme activity. Int. J. Radiat. Biol. 1980; 37: 213–217
   Web of Science ®Google Scholar
• Sharma P., Seshadri T. R., Mukherjee S. K. Some synthetic and natural analogues of glabrachromene. Ind. J. Chem. 1973; 11: 985–986
   Google Scholar
• Shirwaikar A., Malini S., Kumari S. C. Protective effect of Pongamia pinnata flowers against cisplatin and gentamicin induced nephrotoxicity in rats. Ind. J. Exp. Biol. 2003; 41(1)58–62
   PubMedGoogle Scholar
• Simmons K. J. Defense against free radicals has therapeutic implications. JAMA 1972; 251: 2187–2192
   Google Scholar
• Singh R. K., Joshi V., Goel R. K., Gambhir S. S., Acharya S. B. Pharmacological actions of Pongamia pinnata seeds—a preliminary report. Ind. J. Exp. Biol. 1996; 34: 1204–1207
   PubMedGoogle Scholar
• Singh R. K., Pandey B. L. Anti-inflammatory activity of seed extracts of Pongamia pinnata in rats. Ind. J. Phy. Pharm. 1996; 40: 355–358
   PubMedGoogle Scholar
• Sinha K. A. Colorimetric assay of catalase. Anal. Biochem. 1972; 47: 389–394
   PubMed Web of Science ®Google Scholar
• Srinivasan K., Muruganandan S., Lal J., Chandra S., Tandan S. K., Prakash V. R. Evaluation of anti-inflammatory activity of Pongamia pinnata leaves in rats. J. Ethanopharmacol. 2001; 78: 151–157
   PubMed Web of Science ®Google Scholar
• Steinberg D., Parathasarathy S., Carew T. E., Khow J. C., Wiatum J. L. Modifications of low density lipoproteins that increase its atherogenicity. New Eng. J. Med. 1989; 320: 915–918
   PubMed Web of Science ®Google Scholar
• Talapatra S. K., Malik A. K., Talapatra B. Pongaglabol, a new hydroxyfuranoflavone and aurantimide acetate, a despite from the flower of Pongamia glabra. Phytochemistry 1980; 19: 1199–1202
   Web of Science ®Google Scholar
• Talapatra S. K., Malik A. K., Talapatra B. Isopongaglabol and 6-methoxyisopongaglabol, two new hydroxyfuranoflavone from Pongamia glabra. Phytochemistry 1982; 21: 761–766
   Web of Science ®Google Scholar
• Toshiyuki T., Munekazu L., Kaoru Y., Yuko F., Mizuo M. Flavonoids in root bark of Pongamia pinnata. Phytochemistry 1992; 31: 993–998
   Web of Science ®Google Scholar
• Tream W. R. Inherited and acquired syndromes of hyperammonemia and encephalopathy in children. Semin. Liver Dis. 1994; 14: 236–258
   PubMed Web of Science ®Google Scholar
• Trease C. E., Evan V. C. Pharmacopoeial and related drugs of biological origin. Part V. Pharmacognosy. Saunders, London 1959; 161: 466
   Google Scholar
• Varley H., Gowenlock A. H., Bell M. Practical Clinical Biochemistry4th. CBS Publishers. 1988; 1: 161–210
   Google Scholar
• Velvizhi S., Dakshayani K. B., Subramanian P. Effects of alpha ketoglutarate on antioxidants and lipid peroxidation in rats treated with ammonium acetate. Nutrition 2002a; 18: 747–750
   PubMed Web of Science ®Google Scholar
• Velvizhi S., Dakshayani K. B., Subramanian P. Protective influences of alpha ketoglutarate on lipid peroxidation and antioxidant status in ammonium acetate treated rats. Ind. J. Exp. Biol. 2002b; 40: 1183–1186
   PubMedGoogle Scholar
• Vidhya M., Subramanian P. Enhancement of circulatory antioxidants by alpha-ketoglutarate during sodium valproate treatment in Wistar rats. Pol. J. Pharmacol. 2003; 55: 31–36
   PubMedGoogle Scholar
• Wolheim D. F. Preanalytical increase of ammonia in blood specimens from healthy subjects. Clin. Chem. 1984; 30: 906–908
   PubMed Web of Science ®Google Scholar