C ve E vitaminlerinin, kronik olarak alkolle beslenen sıçanlarda beyin dokusu arjinaz aktivitesi, ornitin ve üre düzeylerine etkileri

Amaç: Sıçanlarda uzun süreli alkol kullanımının beyin arjinaz enzim aktivitesi ve ornitin üzerine etkisi ile C ve E vitaminlerinin bu parametreler üzerindeki etkisi araştırıldı. Çalışma Planı: Çalışmada 4-6 aylık, 75 erkek Wistar Albino cinsi sıçan kullanıldı. On beşerlik gruplar halinde beş çalışma grubu oluşturuldu. Birinci gruba alkole eşit kaloride glukoz oral yoldan verilirken, 2. gruba alkol, 3. gruba alkole ek olarak C vitamini, 4. gruba alkole ek olarak E vitamini, 5. gruba alkole ek olarak C ve E vitaminleri 20 hafta süreyle verildi. Yirminci hafta sonunda sıçanlar sakrifiye edildi. Beyin dokusu örneklerinde arjinaz enzim aktivitesi, ornitin ve üre düzeyleri ölçüldü. Bulgular: Beyin dokusu arjinaz aktivitesi, ornitin ve üre düzeyleri tedavi alan gruplarda alkol grubuna oranla anlamlı olarak yüksek bulundu. Sonuç: Kronik alkol kullanımında arttığı bilinen nitrik oksit sentazın (NOS), L-arjinin havuzunun tükenmesine yol açarak arjinaz enzim aktivitesinde azalmaya neden olabileceği, antioksidan vitaminler olarak C ve E vitaminlerinin kullanımının, oksidatif stresi azaltıp arjinaz/NOS yolağını arjinaz lehine çevirebileceği ve olumsuz etkileri bilinen nitrik oksit üretiminin azalmasının söz konusu olabileceği düşünülmektedir. Aynı anda üretimi artan poliaminler bu olumlu etkiyi daha da artırabilecektir. Dolayısı ile kronik alkol kullanımının zararlı etkilerini azaltmada C ve E vitaminlerinden yararlanılabilir.

Effects of vitamin A and E on arginase activity, ornithine and urea levels in brain tissues of rats on long-term alcohol administration

Objectives: The effect of long-term alcohol administration on brain arginase enzyme activity, ornithine and urea levels and the changes induced by administration of vitamins C and E were investigated. Study Design: Seventy-five male Wistar Albino rats between 4-6 months of age were used. Five study groups, each consisting of 15 rats were formed. The first group received oral glucose with a calorie value equivalent to alcohol. The second group received alcohol, the third, fourth and fifth groups received vitamins C, E and C+E, respectively, in addition to alcohol, for 20 weeks. All animals were sacrificed by the end of 20 weeks and arginase activity, ornithine and urea levels were measured in brain tissue samples. Results: In the treatment groups, arginase activities, ornithine and urea levels were significantly higher than the alcohol group (group 2). Conclusion: These results suggest that the nitric oxide synthase (NOS) enzyme which isshown to have increased in chronic alcohol intake, may cause a decrease in arginase enzyme activity via depleting the L-arginine pool. Antioxidant replacement therapy may increase the arginase enzyme activity and therefore lead to a decrease in nitric oxide production which has been shown to have some negative effects. On the other hand, simultaneously increased polyamine production may potentiate the beneficial effects of these vitamins.Thus, vitamins C and E may prove to be effective in reducing the deleterious effects of chronic alcohol consumption.

___

  • 1) Masoero E, Frattini P, Favalli L, Rozza A, Scelsi R, Govoni S. Effect of acute alcohol on ischemiainduced glutamate release and brain damage. Alcohol 2000;22:173-7.
  • 2) Bleich S, Degner D, Javaheripour K, Kurth C, Kornhuber J. Homocysteine and alcoholism. J Neural Transm Suppl 2000;(60):187-96.
  • 3) Özbakış G. Akut alkol intoksikasyonu ve tedavisi. Sendrom 1998;6:96-100.
  • 4) Jenkinson CP, Grody WW, Cederbaum SD. Comparative properties of arginases. Comp Biochem Physiol B Biochem Mol Biol 1996;114:107-32.
  • 5) Rodwell VW. Catabolism of proteins and amino acid metabolism. In: Murray RK, Granner DK, Mayer PA, Rodwell VW, editors. Harper's biochemistry. 23th ed. Norwalk: Appleton and Lange; 1993. p. 293-302.
  • 6) Que LG, Kantrow SP, Jenkinson CP, Piantadosi CA, Huang YC. Induction of arginase isoforms in the lung during hyperoxia. Am J Physiol 1998;275(1 Pt 1):L96-102.
  • 7) Efron DT, Barbul A. Arginine and nutrition in renal disease. J Ren Nutr 1999;9:142-4.
  • 8) Wiesinger H. Arginine metabolism and the synthesis of nitric oxide in the nervous system. Prog Neurobiol 2001;64:365-91.
  • 9) Pou S, Pou WS, Bredt DS, Snyder SH, Rosen GM. Generation of superoxide by purified brain nitric oxide synthase. J Biol Chem 1992;267:24173-6.
  • 10) Carr A, Frei B. Does vitamin C act as a pro-oxidant under physiological conditions? FASEB J 1999; 13:1007-24.
  • 11) Brigelius-Flohe R, Traber MG. Vitamin E: function and metabolism. FASEB J 1999;13:1145-55.
  • 12) Cheeseman KH. Mechanisms and effects of lipid peroxidation. Mol Aspects Med 1993;14:191-7.
  • 13) Uzbay IT, Grewal JS, Wallis CJ, Dungan LF, Lal H. Nitric oxide synthase inhibition attenuates saccharin or ethanol reinforced responding in Long-Ewans rats. Prog Neuropsychopharmacol & Biol Psychiat 1998;22:1411-23.
  • 14) Suresh MV, Sreeranjit Kumar CV, Lal JJ, Indira M. Impact of massive ascorbic acid supplementation on alcohol induced oxidative stress in guinea pigs. Toxicol Lett 1999;104:221-9.
  • 15) Uzbay IT, Oglesby MW. Nitric oxide and substance dependence. Neurosci Biobehav Rev 2001;25:43-52.
  • 16) Motoliu C, Hermenegildo C, Llansola M, Monfort M, Felipo V. Hyperammonemia impairs glutamate-nitric oxide-cGMP pathway in neurons and in rat brain in vivo. In: Yurdaydın C, Bozkaya H, editors. Advances in hepatic encephalopathy and metabolism in liver disease. Ankara: Ankara University Press; 1999.
  • 17) Geyer JW, Dabich D. Rapid method for determination of arginase activity in tissue homogenates. Anal Biochem 1971;39:412-7.
  • 18) Chinard FP. Photometric estimation of proline and ornithine. J Biol Chem 1952;199:91-5.
  • 19) Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem 1951;193:265-75.
  • 20) Tsai GE, Ragan P, Chang R, Chen S, Linnoila VM, Coyle JT. Increased glutamatergic neurotransmission and oxidative stress after alcohol withdrawal. Am J Psychiatry 1998;155:726-32.
  • 21) Calabrese V, Scapagnini G, Latteri S, Colombrita C, Ravagna A, Catalano C, et al. Long-term ethanol administration enhances age-dependent modulation of redox state in different brain regions in the rat: protection by acetyl carnitine. Int J Tissue React 2002;24:97-104.
  • 22) Zima T, Fialova L, Mestek O, Janebova M, Crkovska J, Malbohan I, et al. Oxidative stress, metabolism of ethanol and alcohol-related diseases. J Biomed Sci 2001;8:59-70.
  • 23) Dodd PR, Beckmann AM, Davidson MS, Wilce PA. Glutamate-mediated transmission, alcohol, and alcoholism. Neurochem Int 2000;37:509-33.
  • 24) Lancaster FE. Alcohol and the brain: what's NO got to do with it? Metab Brain Dis 1995;10:125-33.
  • 25) Cook HT, Jansen A, Lewis S, Largen P, O'Donnell M, Reaveley D, et al. Arginine metabolism in experimental glomerulonephritis: interaction between nitric oxide synthase and arginase. Am J Physiol 1994;267(4 Pt 2):F646-53.
  • 26) Ishii N, Ikenaga H, Carmines PK, Aoki Y, Ogawa Z, Saruta T, et al. High glucose augments arginase activity and nitric oxide production in the renal cortex. Metabolism 2004;53:868-74.
  • 27) Kim NN, Christianson DW, Traish AM. Role of arginase in the male and female sexual arousal response. J Nutr 2004;134(10 Suppl):2873-9.
  • 28) Mori M, Gotoh T. Arginine metabolic enzymes, nitric oxide and infection. J Nutr 2004;134(10 Suppl):2820-5.
  • 29) Erbas H, Aydogdu N, Kaymak K. Effects of Nacetylcysteine on arginase, ornithine and nitric oxide in renal ischemia-reperfusion injury. Pharmacol Res 2004;50:523-7.
  • 30) Nordmann R. Oxidative stress from alcohol in the brain. Alcohol Alcohol Suppl 1987;1:75-82.
  • 31) Lecomte E, Herbeth B, Pirollet P, Chancerelle Y, Arnaud J, Musse N, et al. Effect of alcohol consumption on blood antioxidant nutrients and oxidative stress indicators. Am J Clin Nutr 1994;60:255-61.
  • 32) Erisir M, Beytut E, Ozan S, Aksakal M. Effects of dietary vitamin E and selenium on arginase activity in the liver, kidneys, and heart of rats treated with high doses of glucocorticoid. Cell Biochem Funct 2003;21:331-5.
  • 33) Clarkson AN, Liu H, Pearson L, Kapoor M, Harrison JC, Sammut IA, et al. Neuroprotective effects of spermine following hypoxic-ischemic-induced brain damage: a mechanistic study. FASEB J 2004;18:1114-6.
Trakya Üniversitesi Tıp Fakültesi Dergisi-Cover
  • ISSN: 1301-3149
  • Yayın Aralığı: Yılda 2 Sayı
  • Başlangıç: 2018
  • Yayıncı: -
Sayıdaki Diğer Makaleler

Behçet hastalığında subklavian arter psödoanevrizması

Ahmet YILDIRIM, Ahmet IŞIK, Nusret SIRMA, Vedat GENCER

A case of leucocytoclastic vasculitis due to T-cell rich B-cell lymphoma

Barış AKINCI, Selda ÇENELİ, Özden PİŞKİN, Aydanur KARGI, İnci ALACACIOĞLU, Mehmet Ali ÖZCAN

Serolojik rubella enfeksiyonunda avidite testinin klinik değeri: Olgu sunumu

N. Cenk SAYIN, Nefise AHMET, Füsun G. VAROL

C ve E vitaminlerinin, kronik olarak alkolle beslenen sıçanlarda beyin dokusu arjinaz aktivitesi, ornitin ve üre düzeylerine etkileri

Ayşe A. KUNDAK, HAKAN ERBAŞ, Şendoğan GÜLEN, Gülbin DÖKMECİ, Hüseyin ÇELİK, Turgut ÖZCAN

Hepatik ve kemik-eklem tutulumunun ön planda olduğu iki bruselloz olgusu

Zerrin YULUĞKURAL, Sıla AKHAN

Fibro-Osseous pseudotumor of the digits

UFUK USTA, Murat BAŞ, Nasuhi Engin AYDIN, Servet GÜREŞÇİ

Brusellozda akciğer tutulumu: Olgu sunumu

Emrah BATMAZ, Çakır Ebru EDİS, Abdullah ÇİFTÇİ, Sevinç AKKOYUN, Osman N. HATİPOĞLU, Hakan GENÇHALLAÇ

Plasma levels of asymmetric dimethylarginine and total homocysteine in first degree relatives of type 2 diabetic patients

SİBEL GÜLDİKEN, ÇETİN HAKAN KARADAĞ, Muzaffer DEMİR, Ender ARIKAN, Müjdat KARA

Çocuklarda görülen doğuştan boyun kitlelerinin klinik özellikleri

MUSTAFA İNAN, RECEP YAĞIZ, ABDULLAH TAŞ, Süleyman AYVAZ, Servet ADA

İnaktif, proliferatif, hiperplazik endometriyumlarda ve endometriyoid karsinomda proliferatif-apopitotik aktivitenin değerlendirilmesi

UFUK USTA, Naci EDALI, Nasuhi Engin AYDIN