Neuroprotective effects of Alpinia katsumadai against experimental ischemic damage via control of oxidative stress

References

• Au AM, Chan PH, Fishman RA. (1985). Stimulation of phospholipase A2 activity by oxygen-derived free radicals in isolated brain capillaries. J Cell Biochem, 27, 449–453.
   PubMedGoogle Scholar
• Bora KS, Shri R, Monga J. (2011). Cerebroprotective effect of Ocimum gratissimum against focal ischemia and reperfusion-induced cerebral injury. Pharm Biol, 49, 175–181.
   PubMed Web of Science ®Google Scholar
• Brown JE, Rice-Evans CA. (1998). Luteolin-rich artichoke extract protects low density lipoprotein from oxidation in vitro. Free Radic Res, 29, 247–255.
   PubMed Web of Science ®Google Scholar
• Chan PH, Kawase M, Murakami K, Chen SF, Li Y, Calagui B, Reola L, Carlson E, Epstein CJ. (1998). Overexpression of SOD1 in transgenic rats protects vulnerable neurons against ischemic damage after global cerebral ischemia and reperfusion. J Neurosci, 18, 8292–8299.
   PubMed Web of Science ®Google Scholar
• Choi JK, Kim KM, Kim DK, Yeom MH, Koh JY, Jung SJ, Kim HJ, Oh SH, Kim SY, Lee CH. (2009). Topical anti-inflammatory and antipruritic effects of Alpinia katsumadai extracts. J Dermatol Sci, 53, 81–84.
   PubMedGoogle Scholar
• Coyle JT, Puttfarcken P. (1993). Oxidative stress, glutamate, and neurodegenerative disorders. Science, 262, 689–695.
   PubMed Web of Science ®Google Scholar
• Dalle-Donne I, Rossi R, Colombo R, Giustarini D, Milzani A. (2006). Biomarkers of oxidative damage in human disease. Clin Chem, 52, 601–623.
   PubMed Web of Science ®Google Scholar
• Crack PJ, Taylor JM, de Haan JB, Kola I, Hertzog P, Iannello RC. (2003). Glutathione peroxidase-1 contributes to the neuroprotection seen in the superoxide dismutase-1 transgenic mouse in response to ischemia/reperfusion injury. J Cereb Blood Flow Metab, 23, 19–22.
   PubMedGoogle Scholar
• Dawson TM, Dawson VL, Snyder SH. (1992). A novel neuronal messenger molecule in brain: The free radical, nitric oxide. Ann Neurol, 32, 297–311.
   PubMed Web of Science ®Google Scholar
• Dhanasekaran M, Holcomb LA, Hitt AR, Tharakan B, Porter JW, Young KA, Manyam BV. (2009). Centella asiatica extract selectively decreases amyloid beta levels in hippocampus of Alzheimer’s disease animal model. Phytother Res, 23, 14–19.
   PubMed Web of Science ®Google Scholar
• Fujimura M, Morita-Fujimura Y, Kawase M, Copin JC, Calagui B, Epstein CJ, Chan PH. (1999). Manganese superoxide dismutase mediates the early release of mitochondrial cytochrome C and subsequent DNA fragmentation after permanent focal cerebral ischemia in mice. J Neurosci, 19, 3414–3422.
   PubMed Web of Science ®Google Scholar
• Giulivi C, Boveris A, Cadenas E. (1995). Hydroxyl radical generation during mitochondrial electron transfer and the formation of 8-hydroxydesoxyguanosine in mitochondrial DNA. Arch Biochem Biophys, 316, 909–916.
   PubMed Web of Science ®Google Scholar
• Gordon KB, Macrae IM, Carswell HV. (2005). Effects of 17beta-oestradiol on cerebral ischaemic damage and lipid peroxidation. Brain Res, 1036, 155–162.
   PubMed Web of Science ®Google Scholar
• Hall ED, Braughler JM. (1989). Central nervous system trauma and stroke. II. Physiological and pharmacological evidence for involvement of oxygen radicals and lipid peroxidation. Free Radic Biol Med, 6, 303–313.
   PubMed Web of Science ®Google Scholar
• Horiguchi T, Shima H, Suga S, Ogino M, Shimizu K, Toya S, Nagao M, Kawase T. (2002). Transient forebrain ischemia induces expression of serine/threonine protein phosphatase 1 mRNA in the vulnerable regions of gerbil brain. Neurosci Lett, 325, 115–118.
   PubMed Web of Science ®Google Scholar
• Hua SZ, Luo JG, Wang XB, Wang JS, Kong LY. (2009). Two novel monoterpene-chalcone conjugates isolated from the seeds of Alpinia katsumadai. Bioorg Med Chem Lett, 19, 2728–2730.
   PubMedGoogle Scholar
• Hwang IK, Lim SS, Yoo KY, Lee YS, Kim HG, Kang IJ, Kwon HJ, Park J, Choi SY, Won MH. (2008). A phytochemically characterized extract of Cordyceps militaris and cordycepin protect hippocampal neurons from ischemic injury in gerbils. Planta Med, 74, 114–119.
   PubMedGoogle Scholar
• Hwang IK, Yoo KY, Kim DS, Jeong YK, Kim JD, Shin HK, Lim SS, Yoo ID, Kang TC, Kim DW, Moon WK, Won MH. (2004). Neuroprotective effects of grape seed extract on neuronal injury by inhibiting DNA damage in the gerbil hippocampus after transient forebrain ischemia. Life Sci, 75, 1989–2001.
   PubMed Web of Science ®Google Scholar
• Irmak MK, Fadillioglu E, Sogut S, Erdogan H, Gulec M, Ozer M, Yagmurca M, Gozukara ME. (2003). Effects of caffeic acid phenethyl ester and alpha-tocopherol on reperfusion injury in rat brain. Cell Biochem Funct, 21, 283–289.
   PubMed Web of Science ®Google Scholar
• Jeong GS, Li B, Lee DS, Byun E, Kang DG, Lee HS, Kim YC. (2007). Cytoprotective constituents of Alpinia katsumadai seeds against glutamate-induced oxidative injury in HT22 Cells. Nat Prod Sci, 13, 268–271.
   Google Scholar
• Jenner P. (2003). Oxidative stress in Parkinson’s disease. Ann Neurol, 53 Suppl 3, S26–36; discussion S36.
   Google Scholar
• Ji X, Li C, Lu Y, Chen Y, Guo L. (2007). Post-ischemic continuous administration of galantamine attenuates cognitive deficits and hippocampal neurons loss after transient global ischemia in gerbils. Neurosci Lett, 416, 92–95.
   PubMed Web of Science ®Google Scholar
• Kim GW, Lewén A, Copin J, Watson BD, Chan PH. (2001). The cytosolic antioxidant, copper/zinc superoxide dismutase, attenuates blood-brain barrier disruption and oxidative cellular injury after photothrombotic cortical ischemia in mice. Neuroscience, 105, 1007–1018.
   PubMed Web of Science ®Google Scholar
• Kim JH, Kim SH, Lee EJ, Gao J, Wu Z, Mar W, Chang IM. (1998). Radioprotective effect of Lifukang, a Chinese medicinal plants prescription. Nat Prod Sci, 4, 26–31.
   Google Scholar
• Kimura Y, Takahashi S, Yoshida I. (1968). Studies on the constituents of Alpinia. XII. On the constituents of the seeds of Alpinia katsumadai hayata. I. The structure of cardamomin. Yakugaku Zasshi, 88, 239–241.
   PubMedGoogle Scholar
• Kirino T. (1994). Cerebral ischemia and neuronal death. No To Hattatsu, 26, 130–135.
   PubMedGoogle Scholar
• Lawrence BM, Hogg JW, Terhune SJ. (1972). Terpenoids of two amomum species from Thailand. Phytochemistry, 11, 1534–1535.
   Web of Science ®Google Scholar
• Lee MY, Seo CS, Lee JA, Shin IS, Kim SJ, Ha H, Shin HK. (2012). Alpinia katsumadai H(AYATA) seed extract inhibit LPS-induced inflammation by induction of heme oxygenase-1 in RAW264.7 cells. Inflammation, 35, 746–757.
   PubMed Web of Science ®Google Scholar
• Lee SE, Shin HT, Hwang HJ, Kim JH. (2003). Antioxidant activity of extracts from Alpinia katsumadai seed. Phytother Res, 17, 1041–1047.
   PubMed Web of Science ®Google Scholar
• Li M, Chen M, Huang H, Tao W, Cui J, Xiang H. (2011). Neuroprotective effects of active ingredients isolated from Pegasus laternarius on cultured cerebral neurons. Cell Mol Neurobiol, 31, 73–82.
   PubMedGoogle Scholar
• Lohr JB. (1991). Oxygen radicals and neuropsychiatric illness. Some speculations. Arch Gen Psychiatry, 48, 1097–1106.
   PubMed Web of Science ®Google Scholar
• Mattson MP, Culmsee C, Yu ZF. (2000). Apoptotic and antiapoptotic mechanisms in stroke. Cell Tissue Res, 301, 173–187.
   PubMed Web of Science ®Google Scholar
• McCord JM, Roy RS, Schaffer SW. (1985). Free radicals and myocardial ischemia. The role of xanthine oxidase. Adv Myocardiol, 5, 183–189.
   PubMedGoogle Scholar
• Murakami K, Kondo T, Kawase M, Li Y, Sato S, Chen SF, Chan PH. (1998). Mitochondrial susceptibility to oxidative stress exacerbates cerebral infarction that follows permanent focal cerebral ischemia in mutant mice with manganese superoxide dismutase deficiency. J Neurosci, 18, 205–213.
   PubMed Web of Science ®Google Scholar
• Nade VS, Kawale LA, Dwivedi S, Yadav AV. (2010). Neuroprotective effect of Hibiscus rosa sinensis in an oxidative stress model of cerebral post-ischemic reperfusion injury in rats. Pharm Biol, 48, 822–827.
   PubMed Web of Science ®Google Scholar
• Radi R, Rodriguez M, Castro L, Telleri R. (1994). Inhibition of mitochondrial electron transport by peroxynitrite. Arch Biochem Biophys, 308, 89–95.
   PubMed Web of Science ®Google Scholar
• Radi R, Sims S, Cassina A, Turrens JF. (1993). Roles of catalase and cytochrome c in hydroperoxide-dependent lipid peroxidation and chemiluminescence in rat heart and kidney mitochondria. Free Radic Biol Med, 15, 653–659.
   PubMedGoogle Scholar
• Rajasankar S, Manivasagam T, Surendran S. (2009). Ashwagandha leaf extract: A potential agent in treating oxidative damage and physiological abnormalities seen in a mouse model of Parkinson’s disease. Neurosci Lett, 454, 11–15.
   PubMed Web of Science ®Google Scholar
• Saberi M, Rezvanizadeh A, Bakhtiarian A. (2008). The antiepileptic activity of Vitex agnus castus extract on amygdala kindled seizures in male rats. Neurosci Lett, 441, 193–196.
   PubMed Web of Science ®Google Scholar
• Saiki Y, Ishikawa Y, Uchida M, Fukushima S. (1978). Essential oil from Chinese drug ‘caodoukou’, the seeds of Alpinia katsumadai. Phytochemistry, 17, 808–809.
   Google Scholar
• Sayre LM, Smith MA, Perry G. (2001). Chemistry and biochemistry of oxidative stress in neurodegenerative disease. Curr Med Chem, 8, 721–738.
   PubMed Web of Science ®Google Scholar
• Sevanian A, Muakkassah-Kelly SF, Montestruque S. (1983). The influence of phospholipase A2 and glutathione peroxidase on the elimination of membrane lipid peroxides. Arch Biochem Biophys, 223, 441–452.
   PubMed Web of Science ®Google Scholar
• Suc I, Meilhac O, Lajoie-Mazenc I, Vandaele J, Jürgens G, Salvayre R, Nègre-Salvayre A. (1998). Activation of EGF receptor by oxidized LDL. FASEB J, 12, 665–671.
   PubMed Web of Science ®Google Scholar
• Sugawara T, Noshita N, Lewén A, Gasche Y, Ferrand-Drake M, Fujimura M, Morita-Fujimura Y, Chan PH. (2002). Overexpression of copper/zinc superoxide dismutase in transgenic rats protects vulnerable neurons against ischemic damage by blocking the mitochondrial pathway of caspase activation. J Neurosci, 22, 209–217.
   PubMedGoogle Scholar
• Won MH, Kang TC, Jeon GS, Lee JC, Kim DY, Choi EM, Lee KH, Choi CD, Chung MH, Cho SS. (1999). Immunohistochemical detection of oxidative DNA damage induced by ischemia-reperfusion insults in gerbil hippocampus in vivo. Brain Res, 836, 70–78.
   PubMed Web of Science ®Google Scholar
• Yang J, Dai Y, Xia YF, Huang WZ, Wang ZT. (2009). Alpinia katsumadai Hayata prevents mouse sepsis induced by cecal ligation and puncture through promoting bacterial clearance and downregulating systemic inflammation. Phytother Res, 23, 267–273.
   PubMedGoogle Scholar
• Yang Y, Kinoshita K, Koyama K, Takahashi K, Tai T, Nunoura Y, Watanabe K. (1999). Two novel anti-emetic principles of Alpinia katsumadai. J Nat Prod, 62, 1672–1674.
   PubMedGoogle Scholar
• Yushiro K, Shuhiti T, Ikuo Y. (1968). Studies on the constituents of the seeds of Alpinia katsumadai. Yakugaku Zasshi, 88, 239–241.
   PubMedGoogle Scholar
• Zhang Y, Marcillat O, Giulivi C, Ernster L, Davies KJ. (1990). The oxidative inactivation of mitochondrial electron transport chain components and ATPase. J Biol Chem, 265, 16330–16336.
   PubMed Web of Science ®Google Scholar
• Zheng M, Liu C, Pan F, Shi D, Ma F, Zhang Y, Zhang Y. (2011). Protective effects of flavonoid extract from Apocynum venetum leaves against corticosterone-induced neurotoxicity in PC12 cells. Cell Mol Neurobiol, 31, 421–428.
   PubMedGoogle Scholar