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Evaluation of the effects of Cyclotrichium niveum on brain acetylcholinesterase activity and oxidative stress in male rats orally exposed to lead acetate
Corresponding Author(s) : Zafer Sahin
Cellular and Molecular Biology,
Vol. 65 No. 5: Issue 5
Abstract
Cyclotrichium niveum is an endemic plant for Turkey and it appears to have in vitro antioxidant and acetylcholinesterase inhibition properties. To the best of our knowledge, there has been no study on the in vivo effects of this plant. Therefore, the purpose of this study was to evaluate the effects of C. niveum on lead (Pb)-acetate-induced potential alterations in brain acetylcholinesterase activity, as well as oxidative stress in male rats. The rats were randomly assigned to control, Pb-acetate, C. niveum and Pb-acetate+ C. niveum groups. Pb-acetate was provided in drinking water (500 ppm), and C. niveum was administered via orogastric gavage (4 ml/kg) for 30 days. The acetylcholinesterase activity in the brain significantly decreased only in the Pb-acetate group. The malondialdehyde level significantly increased, and the reduced glutathione activity decreased in the Pb-acetate group. The reduced glutathione and glutathione-S-transferase activities of the C. niveum group were higher than the control group. No Pb was detected on a ppb level in the brain tissue of the control and C. niveum groups, while it was detected in the brains of the rats in the Pb-acetate and Pb-acetate+ C. niveum groups (185+8.98 ppb and 206+56.65 ppb, respectively). The data collected in this study suggested that C. niveum may reduce inhibition of brain AChE activity and oxidative stress against Pb-acetate-induced alterations in the brain of male rats.
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- Gracia RC, Snodgrass WR. Lead toxicity and chelation therapy. Am J Health Syst Pharm 2007; 64:45-53.
- Demirdag R, Comakli V, Ozkaya A, Sahin Z, Dag U, Yerlikaya E, et al. Examination of changes in enzyme activities of erythrocyte glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase in rats given Naringenin and Lead acetate. J Biochem Mol Toxicol 2015; 29(1):43-7.
- Ozkaya A, Sahin Z, Dag U, Ozkaraca M. Effects of Naringenin on Oxidative Stress and Histopathological Changes in the Liver of Lead Acetate Administered Rats. J Biochem Mol Toxicol 2016; 30(5):243-8.
- Abdel Moneim AE. Flaxseed oil as a neuroprotective agent on lead acetate-induced monoamineric alterations and neurotoxicity in rats. Biol Trace Elem Res 2012; 148:363–370.
- Abdel Moneim AE, Dkhil MA, Al-Quraishy S. Effects of flaxseed oil on lead acetate-induced neurotoxicity in rats. Biol Trace Elem Res 2011; 144(1-3):904-13.
- Strohl WR. 2000. The role of natural products in a modern drug discovery program. Drug Discov Today 2000; 5(2):39-41.
- Baser KHC, Sarikardasoglu S, Tümen G. The Essential Oil of Cyclotrichium niveum (Boiss.) Manden. Et Scheng. J Essen Oil Res 1994; 6:9-12.
- Baytop T. Turkce bitki adlari sozlugu (A dictionary of vernacular names of wild plants of Turkey). Publication of the Turk Dil Kurumu (The Turkish Language Society), Ankara, 1997 vol. 578.
- Gülcin I, Tel AZ, Kirecci E. Antioxidant, antimicrobial, antifungal, and antiradical activities of Cyclotrichium niveum (Boiss.) Manden & Scheng. Int J Food Crops 2008; 11:450–471.
- Cetinus SA, Goze I, Sarac B, Vural N. Scavenging effect and antispasmodic activity of the essential oil of Cyclotrichium niveum. Fitoterapia 2007; 78(2):129-133.
- Emen S, Ceken B, Kizil G, Kizil M. DNA damage protecting activity and in vitro antioxidant potential of the methanol extract of Cyclotrichium niveum. Pharm Biol 2009; 47(3): 219-229.
- Gursoy N, Sihoglu-Tepe A, Tepe B. Determination of in vitro antioxidative and antimicrobial properties and total phenolic contents of Ziziphora clinopodioides, Cyclotrichium niveum, and Mentha longifolia ssp. typhoides var. typhoides. J Med Food 2009; 12(3):684-689.
- Orhan I, Senol FS, Gülpinar AR, Kartal M, Sekeroglu N, Deveci M, et al. Acetylcholinesterase inhibitory and antioxidant properties of Cyclotrichium niveum, Thymus praecox subsp. caucasicus var. caucasicus, Echinacea purpurea and E. pallida. Food Chem Toxicol 2009; 47:1304-1310.
- Reddy GR, Basha MR, Devi CB, Suresh A, Baker JL, Shafeek A, et al. Lead induced effects on acetylcholinesterase activity in cerebellum and hippocampus of developing rat. Int J Dev Neurosci 2003; 21(6):347–352.
- Basha DC, Rani MU, Devi CB, Kumar MR, Reddy GR. Perinatal lead exposure alters postnatal cholinergic and aminergic system in rat brain: reversal effect of calcium co-administration. Int J Dev Neurosci 2012; 30:343-350.
- Phyu MP, Tangpong J. Neuroprotective effects of xanthone derivative of Garcinia mangostana against lead-induced acetylcholinesterase dysfunction and cognitive impairment. Food Chem Toxicol 2014; 70:151-6.
- Tangpong J, Satarug S. Alleviation of lead poisoning in the brain with aqueous leaf extract of the Thunbergia laurifolia (Linn.). Toxicol Lett 2010; 198:83-88.
- Ellman GL, Andres DC. New and rapid colorimetric determination of aceytlcholinesterase activity. Biochem Pharmacol 1961; 7:88–95.
- Ozmen M, Dominguez SE, Fairbrother A. Effects of dietary azinphos methyl on selected plasma and tissue biomarkers of the gray-tailed vole. Bull Environ Contam Toxicol 1998; 60:194-201.
- Bradford MM. A rapid sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976; 72:248–254.
- Placer ZA, Cushman LL, Johnson BC. Estimation of product of lipid peroxidation (malonyl dialdehyde) in biochemical systems. Analytical biochemistry 1966; 16:359–364.
- Moron MS, Depierre JW, Mannervik B. Levels of glutathione, glutathione reductase and glutathione S-transferase activities in rat lung and liver. Biochim Biophys Acta 1979; 582:67–78.
- Carlberg I, Mannervik B. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. J Biol Chem 1975; 250:5475–5480.
- Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J Biol Chem 1974; 249(22):7130–7139.
- Rattanachongkiat S, Millward GE, Foulkes ME. Determination of arsenic species in fish, crustacean and sediment samples from Thailand using high performance liquid chromatography (HPLC) coupled with inductively coupled plasma mass spectrometry (ICP-MS). J Environ Monit 2004; 6(4):254-61.
- De Blas Bravo I, Sanz Castro R, López Riquelme N, Tormo Díaz C, Apraiz Goyenaga D. Optimization of the trace element determination by ICP-MS in human blood serum. J Trace Elem Med Biol 2007; 21(Suppl 1):14-7.
- Tüzmen MN, Yücel NC, Kalburcu T, Demiryas N. Effects of curcumin and tannic acid on the aluminum- and lead-induced oxidative neurotoxicity and alterations in NMDA receptors. Toxicol Mech Methods. 2015; 25(2):120-7.
- Pedroso TF, Oliveira CS, Fonseca MM, Oliveira VA, Pereira ME. Effects of Zinc and N-Acetylcysteine in Damage Caused by Lead Exposure in Young Rats. Biol Trace Elem Res 2017; 180(2):275-284.
- Inan M, Tel AZ. Determination of Cyclotrichium niveum Essential Oil and Its Components at Different Altitudes. Not Bot Horti Agrobo 2014; 42(1):128-131.
- Shukla PK, Khanna VK, Khan MY, Srimal RC. Protective effect of curcumin against lead neurotoxicity in rat. Hum Exp Toxicol 2003; 22(12):653-8.
- Saxena G, Pathak U, Flora SJS. Beneficial role of monoesters of meso-2,3- dimercaptosuccinic acid in the mobilization of lead and recovery of tissue oxidative injury in rats. Toxicology 2005; 214:39–56.
- Parke DV, Piotrowski J. Glutathione: Its role in detoxication of reactive oxygen and environmental chemicals. Acta Pol Toxicol 1996; 4:1-14.
- Dringer A. Metabolism and function of glutathione in brain. Prog Neurobiol 2000; 62(6):649-71.
- Reed DJ. Glutathione: Toxicological implications. Annu Rev Pharmacol Toxicol 1990; 30:603-31.
- Strange C, Jones PW, Fryer AA. Glutathione S-transferase: genetics and role in toxicology. Toxicol Lett 2000; 112-113:357-63.
- Boon PJ, Marinho HS, Oosting R, Mulder GJ. Glutathione conjugation of 4-hydroxy-trans-2.3-nonenal in the rat in vivo, the isolated perfused liver and erythrocytes. Toxicol Appl Pharmacol. 1999; 159(3):214-23.
- Laurent A, Perdu-Durand E, Alary J, Debrauwer L, Cravedi JP. Metabolism of 4-hydroxynonenal, a cytotoxic product of lipid peroxidation, in rat precision-cut liver slices. Toxicol Lett 2000; 114(1-3):203-14.
- Liu CM, Ma JQ, Sun YZ. Protective role of puerarin on lead-induced alterations of the hepatic glutathione antioxidant system and hyperlipidemia in rats. Food Chem Toxicol 2011; 49(12):3119-27.
References
Gracia RC, Snodgrass WR. Lead toxicity and chelation therapy. Am J Health Syst Pharm 2007; 64:45-53.
Demirdag R, Comakli V, Ozkaya A, Sahin Z, Dag U, Yerlikaya E, et al. Examination of changes in enzyme activities of erythrocyte glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase in rats given Naringenin and Lead acetate. J Biochem Mol Toxicol 2015; 29(1):43-7.
Ozkaya A, Sahin Z, Dag U, Ozkaraca M. Effects of Naringenin on Oxidative Stress and Histopathological Changes in the Liver of Lead Acetate Administered Rats. J Biochem Mol Toxicol 2016; 30(5):243-8.
Abdel Moneim AE. Flaxseed oil as a neuroprotective agent on lead acetate-induced monoamineric alterations and neurotoxicity in rats. Biol Trace Elem Res 2012; 148:363–370.
Abdel Moneim AE, Dkhil MA, Al-Quraishy S. Effects of flaxseed oil on lead acetate-induced neurotoxicity in rats. Biol Trace Elem Res 2011; 144(1-3):904-13.
Strohl WR. 2000. The role of natural products in a modern drug discovery program. Drug Discov Today 2000; 5(2):39-41.
Baser KHC, Sarikardasoglu S, Tümen G. The Essential Oil of Cyclotrichium niveum (Boiss.) Manden. Et Scheng. J Essen Oil Res 1994; 6:9-12.
Baytop T. Turkce bitki adlari sozlugu (A dictionary of vernacular names of wild plants of Turkey). Publication of the Turk Dil Kurumu (The Turkish Language Society), Ankara, 1997 vol. 578.
Gülcin I, Tel AZ, Kirecci E. Antioxidant, antimicrobial, antifungal, and antiradical activities of Cyclotrichium niveum (Boiss.) Manden & Scheng. Int J Food Crops 2008; 11:450–471.
Cetinus SA, Goze I, Sarac B, Vural N. Scavenging effect and antispasmodic activity of the essential oil of Cyclotrichium niveum. Fitoterapia 2007; 78(2):129-133.
Emen S, Ceken B, Kizil G, Kizil M. DNA damage protecting activity and in vitro antioxidant potential of the methanol extract of Cyclotrichium niveum. Pharm Biol 2009; 47(3): 219-229.
Gursoy N, Sihoglu-Tepe A, Tepe B. Determination of in vitro antioxidative and antimicrobial properties and total phenolic contents of Ziziphora clinopodioides, Cyclotrichium niveum, and Mentha longifolia ssp. typhoides var. typhoides. J Med Food 2009; 12(3):684-689.
Orhan I, Senol FS, Gülpinar AR, Kartal M, Sekeroglu N, Deveci M, et al. Acetylcholinesterase inhibitory and antioxidant properties of Cyclotrichium niveum, Thymus praecox subsp. caucasicus var. caucasicus, Echinacea purpurea and E. pallida. Food Chem Toxicol 2009; 47:1304-1310.
Reddy GR, Basha MR, Devi CB, Suresh A, Baker JL, Shafeek A, et al. Lead induced effects on acetylcholinesterase activity in cerebellum and hippocampus of developing rat. Int J Dev Neurosci 2003; 21(6):347–352.
Basha DC, Rani MU, Devi CB, Kumar MR, Reddy GR. Perinatal lead exposure alters postnatal cholinergic and aminergic system in rat brain: reversal effect of calcium co-administration. Int J Dev Neurosci 2012; 30:343-350.
Phyu MP, Tangpong J. Neuroprotective effects of xanthone derivative of Garcinia mangostana against lead-induced acetylcholinesterase dysfunction and cognitive impairment. Food Chem Toxicol 2014; 70:151-6.
Tangpong J, Satarug S. Alleviation of lead poisoning in the brain with aqueous leaf extract of the Thunbergia laurifolia (Linn.). Toxicol Lett 2010; 198:83-88.
Ellman GL, Andres DC. New and rapid colorimetric determination of aceytlcholinesterase activity. Biochem Pharmacol 1961; 7:88–95.
Ozmen M, Dominguez SE, Fairbrother A. Effects of dietary azinphos methyl on selected plasma and tissue biomarkers of the gray-tailed vole. Bull Environ Contam Toxicol 1998; 60:194-201.
Bradford MM. A rapid sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976; 72:248–254.
Placer ZA, Cushman LL, Johnson BC. Estimation of product of lipid peroxidation (malonyl dialdehyde) in biochemical systems. Analytical biochemistry 1966; 16:359–364.
Moron MS, Depierre JW, Mannervik B. Levels of glutathione, glutathione reductase and glutathione S-transferase activities in rat lung and liver. Biochim Biophys Acta 1979; 582:67–78.
Carlberg I, Mannervik B. Purification and characterization of the flavoenzyme glutathione reductase from rat liver. J Biol Chem 1975; 250:5475–5480.
Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J Biol Chem 1974; 249(22):7130–7139.
Rattanachongkiat S, Millward GE, Foulkes ME. Determination of arsenic species in fish, crustacean and sediment samples from Thailand using high performance liquid chromatography (HPLC) coupled with inductively coupled plasma mass spectrometry (ICP-MS). J Environ Monit 2004; 6(4):254-61.
De Blas Bravo I, Sanz Castro R, López Riquelme N, Tormo Díaz C, Apraiz Goyenaga D. Optimization of the trace element determination by ICP-MS in human blood serum. J Trace Elem Med Biol 2007; 21(Suppl 1):14-7.
Tüzmen MN, Yücel NC, Kalburcu T, Demiryas N. Effects of curcumin and tannic acid on the aluminum- and lead-induced oxidative neurotoxicity and alterations in NMDA receptors. Toxicol Mech Methods. 2015; 25(2):120-7.
Pedroso TF, Oliveira CS, Fonseca MM, Oliveira VA, Pereira ME. Effects of Zinc and N-Acetylcysteine in Damage Caused by Lead Exposure in Young Rats. Biol Trace Elem Res 2017; 180(2):275-284.
Inan M, Tel AZ. Determination of Cyclotrichium niveum Essential Oil and Its Components at Different Altitudes. Not Bot Horti Agrobo 2014; 42(1):128-131.
Shukla PK, Khanna VK, Khan MY, Srimal RC. Protective effect of curcumin against lead neurotoxicity in rat. Hum Exp Toxicol 2003; 22(12):653-8.
Saxena G, Pathak U, Flora SJS. Beneficial role of monoesters of meso-2,3- dimercaptosuccinic acid in the mobilization of lead and recovery of tissue oxidative injury in rats. Toxicology 2005; 214:39–56.
Parke DV, Piotrowski J. Glutathione: Its role in detoxication of reactive oxygen and environmental chemicals. Acta Pol Toxicol 1996; 4:1-14.
Dringer A. Metabolism and function of glutathione in brain. Prog Neurobiol 2000; 62(6):649-71.
Reed DJ. Glutathione: Toxicological implications. Annu Rev Pharmacol Toxicol 1990; 30:603-31.
Strange C, Jones PW, Fryer AA. Glutathione S-transferase: genetics and role in toxicology. Toxicol Lett 2000; 112-113:357-63.
Boon PJ, Marinho HS, Oosting R, Mulder GJ. Glutathione conjugation of 4-hydroxy-trans-2.3-nonenal in the rat in vivo, the isolated perfused liver and erythrocytes. Toxicol Appl Pharmacol. 1999; 159(3):214-23.
Laurent A, Perdu-Durand E, Alary J, Debrauwer L, Cravedi JP. Metabolism of 4-hydroxynonenal, a cytotoxic product of lipid peroxidation, in rat precision-cut liver slices. Toxicol Lett 2000; 114(1-3):203-14.
Liu CM, Ma JQ, Sun YZ. Protective role of puerarin on lead-induced alterations of the hepatic glutathione antioxidant system and hyperlipidemia in rats. Food Chem Toxicol 2011; 49(12):3119-27.