Yüksek doz prednizolon enjekte edilmiş ratların karaciğer böbrek ve kalp alkalin fosfataz aktivitesi üzerine oral vitamin E ve /veya selenyumun etkisi

Yüksek doz prednizolon uygulanan ratlarda alkalin fosfataz (ALP) aktivitesi üzerine E vitamini ve Selenyum (Se) ilavesinin etkileri araştırıldı. 210 adet rat 5 gruba ayrıldı (ilk grup 10 rat, diğer her grup 50 rat). Ratlar normal bir diyetle beslendi, fakat 3, 4 ve 5. gruplara oral gavaj ile sırasıyla 20 mg E vitamini, 0.3 mg Se ve bunların kombinasyonları 30 gün boyunca günlük olarak içirildi. Bu uygulamadan sonraki 3 gün kontrole (grup 1) serum fizyolojik, diğer 4 gruba (2, 3, 4 ve 5. grup) ise prednizolon (100 mg/kg canlı ağırlık) intramuskular uygulandı. Prednizolonun son uygulanmasını takiben kontrol grubu hariç, diğer her gruptan 10 adet rat 4, 8, 12, 24 ve 48. saatlerde öldürülerek, karaciğer, böbrek ve kalplerindeki ALP aktiviteleri belirlendi. Yüksek doz prednizolon, 4 ile 24. saatler arasında, ALP aktivitesinin karaciğer dokusunda önemli olarak artmasına, kalp dokusunda önemli azalmasına sebep olmakta, böbrek dokusundaki aktiviteyi ise etkilememektedir. Vitamin E ilavesi, tüm zaman birimlerinde kontrole ve sadece prednizolon uygulanan gruba göre karaciğer ve böbrek ALP aktivitesinde artışa sebep oldu. Vitamin E ilavesi sadece prednizolon uygulanan gruba göre özellikle 4, 8, ve 12. saatlerde kalp ALP aktivitesini önemli derecede arttırarak aktiviteleri normale döndürdü. Se ilavesi sadece prednizolon uygulanan grupla karşılaştırıldığında 4. saatten itibaren karaciğer ALP aktivitesini azaltmakta ve prednizolonun sebep olduğu ALP aktivitesindeki artışları önlemekte, 24 ve 48. saatte ise ALP aktivitesini hem kontrole hem de sadece prednizolon uygulanan gruba göre önemli olarak azaltmaktadır. Se ilavesinin rat böbrek ALP aktivitesi üzerine herhangi bir etkisi saptanmadı. Kalp dokusunda ise Se hem kontrol grubuna hemde sadece prednizolon uygulanan gruba göre ALP aktivitesinin azalmasına sebep olmaktadır. Karaciğer ve böbrekte kombine grupta tüm zaman birimlerinde aktivitenin kontrol değerlerine yakın olduğu tespit edildi. Kalpte ise vitamin E ve Se kombinasyonunun ilavesi sadece prednizolon uygulanan gruba ve kontrol grubuna göre ALP aktivitesinin önemli azalmasına sebep oldu. Prednizolon uygulanan ratlarda, çalışılan dokularda genelde vitamin E ilavesi ALP aktivitesini arttırıcı, Se ise azaltıcı etkiye sahipti. ALP aktivitesinde meydana gelen azalmalar vitamin E ilavesi ile ALP aktivitesinde meydana gelen artışlar ise Se ilavesi ile engellenebilir.

Effects of oral vitamin E and/or selenium on alkaline phosphatase activity in the liver, kindneys and heart of prednisolone-injected rats

The effects of dietary intake vitamin E and Se on alkaline phosphatase (ALP) activity in rats treated with high doses of prednisolone were investigated. 210 rats were divided into five groups (50 rats per groups, except for the first group with 10 rats). The rats were fed a normal diet, but groups 3, 4, and 5 received a daily supplement with oral gavage the 20 mg vitamin E, 0.3 mg Se, and a combination of vitamin E and Se, respectively, for 30 days. For 3 days subsequently, the control group (group 1) was given a placebo, and the remaining 4 groups (groups 2, 3, 4, and 5) were injected intramuscularly with 100 mg kg-1 body weight prednisolone. After the last administration of prednisolone, 10 rats from each of the groups other than the control were killed at 4, 8, 12, 24, and 48h and the activity ALP enzyme in the liver, kidneys and heart was measured. In the group treated with prednisolone alone, ALP activity in the liver was significantly increased between 4 and 24 h, in the heart were significantly decreased. ALP activity in the kidneys was not affected by prednisolone. Compared to the control and prednisolone groups, ALP activity in the liver and kidneys of the vitamin E supplemented groups was found to be increased at all time periods. Compared to the prednisolone group, ALP activity in the heart was significantly increased in the vitamin E administered group between 4 and 12 h, recovered to the control level at 24 and 48 h. Compared to the prednisolone groups, ALP activity in the liver was decreased significantly in the Se administered group after 4 h. The increment in the liver ALP activity induced by prednisolone was reduced by Se supplementation. But compared to both the control and prednisolone groups, the ALP activity was significantly decreased in the Se administered group at 24 and 48 h. ALP activity in the kidneys was not affected by Se supplementation. Compared to both the control and prednisolone groups, ALP activity in the heart was decreased in the Se administered group at all time periods. No significant differences were found at any time period in the liver and kidneys ALP activity in the combination group compared to the control. Compared to both the control and prednisolone groups, ALP activity in the heart was significantly decreased in the combination group. The present study demonstrates that in rats treated with prednisolone, generally, vitamin E supplementation increases ALP activity, but Se supplementation decreases. Therefore, vitamin E supplementation may prevent the decreases in ALP activity, Se supplementation may prevent the increases.

___

  • 1.Joseph J, Devkar RV, Ramachandran AV: Effect of dexamethasone and corticosterone on activity levels of ATPase, phosphomonoesterases and phosphodiesterase in liver, muscle and testis of post-hatched white leghorn chicks. Indian J Exp Biol, 35, 977-982, 1997.
  • 2.Zernik J, Kream B, Twarog K: Tissue-specific and dexamethasone-inducible expression of alkaline phosphatase from alternative promoters of the rat bone/liver/kidney/ placenta gene. Biochem Biophys Res Commun, 176 (3): 1149-1156, 1991.
  • 3.Gallo-Torres HE: Absorption, Blood Transport and Metabolism of Vitamin E. In, Machlin LJ (Ed): Vitamin E: A Comprehensive Treatise. pp. 170-267, Marcel-Dekker, New York, 1980.
  • 4.Schwarz K, Folz CM: Selenium as an integral part of factor 3 against dietary liver degeneration. J Am Chem Soc, 79, 3292-3293, 1957.
  • 5.Kalender S, Ogutcu A, Uzunhisarcikli M, Açikgoz F, Durak D, Ulusoy Y, Kalender Y: Diazinon-induced hepatotoxicity and protective effect of vitamin E on some biochemical indices and ultrastructural changes. Toxicol, 211, 197-206, 2005.
  • 6.Bansal KA, Bansal M, Soni G, Bhatnagar D: Protective role of vitamin E pre-treatment on N-nitrosodiethylamine induced oxidative stress in rat liver. Chem Biol Interact, 156, 101-111, 2005.
  • 7.Mostafavi-Pour Z, Zal F, Monabati A, Vessal M: Protective effects of a combination of quercetin and vitamin E against cyclosporine A-induced oxidative stress and hepatotoxicity in rats. Hepatol Res, 38, 385-392, 2008.
  • 8.Shrivastava S, Jadon A, Shukla S: Effect of tiron and its combination with nutritional supplements against vanadium intoxication in female albino rats. J Toxicol Sci, 32, 185-192, 2007.
  • 9.Liu GJ, Zhao JH, Liu JY, Wang LX: Effect of selenium-enriched malt on hepatocarcinogenesis, paraneoplastic syndrome and the hormones regulating blood glucose in rats treated by diethylnitrosamine. Life Sci, 78, 2315-2321, 2006.
  • 10.El-Demerdash MF: Antioxidant effect of vitamin E and selenium on lipid peroxidation, enzyme activities and biochemical parameters in rats exposed to aluminium. J Trace Elem Med Biol, 18, 113-121, 2004.
  • 11.Pekarthy MJ, Short J, Lansing IA, Lieberman I: Function and control of liver alkaline phosphatase. J Biol Chem, 247 (6): 1767-1774, 1972.
  • 12.Jung W, Gebhardt R, Mecke D: Alterations in activity and ultrastructural localization of several phosphatases on the surface of adult rat hepatocytes in primary monolayer culture. Eur J Cell Biol, 27 (2): 230-241, 1982.
  • 13.Freeman RH, Rostorfer HH: Hepatic changes in renin substrate biosynthesis and alkaline phosphatase activity in the rat. Am J Physiol, 223 (2): 364-370, 1972.
  • 14.Donald S, Verschoyle DR, Greaves P, Orr S, Jimeno J, Gescher JA: Comparison of four modulators of drug metabolism as protectants against the hepatotoxicity of the novel antitumor drug yondelis (ET-743) in the female rat and in hepatocytes in vitro. Cancer Chemother Pharmacol, 53, 305312, 2004.
  • 15.Bessey OA, Lowry OH, Brock MJ: A Method for the rapid determination of alkaline phosphatase with five cubic millimeters of serum. J Biol Chem, 164, 321-323, 1946.
  • 16.Henriquez-Hernandez LA, Flores-Morales A, Santana Farre R, Axelson M, Nilsson P, Norstedt G, Fernandez-Perez L: Role of pituitary hormones on 17α-ethinylestradiol-induced cholestasis in rat. J Pharmacol Exp Ther, 320, 695-705, 2007.
  • 17.Melani F, Farnararo M, Chiarugi VP: Molecular aspects of the regulation of rat kidney alkaline phosphatase. Biochem J, 121, 33-40, 1971.
  • 18.Yora T, Sakagishi Y, Tashima Y, Kumegawa M: Effects of dibutyryl adenosine 3’:5’-cyclic monophosphate and other agents on induction of alkaline phosphatase activity in monkey kidney cells. J Biochem, 95, 369-376, 1984.
  • 19.Brière N: Effect of hormones on hydrolase activities and DNA synthesis in kidney of the developing mouse. Can J Physiol Pharmacol, 66 (5): 580-585, 1988.
  • 20.Bertrand L, Briere N: Effect of hydrocortisone on the maturation of human foetal kidney explants in serum-free organ culture. Biochem Cell Biol, 67, 121-127, 1989.
  • 21.Dey KS, Nayak P, Roy S: Alpha-tocopherol supplementation on chromium toxicity: A study on rat liver and kidney cell membrane. J Environ Sci, 15 (3): 356-359, 2003.
  • 22.El-Demerdash MF, Yousef IM, Kedwany SF, Baghdadi HH: Cadmium-induced changes in lipid peroxidation, blood hematology, biochemical parameters and semen quality of male rats: Protective role of vitamin E and β-carotene. Food Chem Toxicol, 42, 1563-1571, 2004.
  • 23.Montilla P, Cruz A, Padillo JF, Tunez I, Gascon F, Munoz MC, Gomez M, Pera C: Melatonin versus vitamin E as protective treatment against oxidative stress after extra-hepatic bile duct ligation in rats. J Pineal Res, 31, 138-144, 2001.
  • 24.Flora SJS, Behari RJ, Ashquin M, Tandon KS: Time-dependent protective effect of selenium against cadmium-induced nephrotoxicity and hepatotoxicity. Chem Biol Int, 42, 345-351, 1982.
  • 25.Meydani M: Modulation of platelet thromboxane A2 and aortic prostacyclin synthesis by dietary selenium and Vitamin E. Biol Trace Elem Res, 33, 79-86, 1992.
Kafkas Üniversitesi Veteriner Fakültesi Dergisi-Cover
  • ISSN: 1300-6045
  • Yayın Aralığı: Yılda 6 Sayı
  • Başlangıç: 1995
  • Yayıncı: Kafkas Üniv. Veteriner Fak.
Sayıdaki Diğer Makaleler

Kene ısırığı nedeniyle Kaş Devlet Hastanesi acil servisine başvuran Hastaların değerlendirilmesi

Aziz SÜMER

Geçiş dönemindeki süt ineklerinin beslenmesi ll. bu dönemde görülen metabolik hastalıklar ve beslenme ile önlenmesi

CAVİT ARSLAN, Tuncay TUFAN

Determination of heavy metal levels in fish samples collected from the Middle Black Sea

CEVAT NİSBET, GÖKNUR TERZİ GÜLEL, Osman PİLGİR, Neslihan SARAC

The effect of air pressure with cervical artificial insemination on the fertility of awassi ewes synchronized with $PGF2alpha$

Abuzer Kafar ZONTURLU, Ümit YAVUZER, Faruk ARAL

A case of lobulated spleen in a Holstein cow

Ayşe HALIGÜR, ÖZLEM ÖZMEN, MEHMET HALIGÜR

Türkiye'de ticari broyler işletmelerinden vanA pozitif Enterococcus faecium izolasyonu

NİLGÜN ÜNAL, Zahide DİLİK, MURAT YILDIRIM

Proantosiyanidinin allograft renal oksidatif stresi önleyici etkisi: deneysel bir çalışma

Orhan YÜCEL, Adem GÜLER, MEHMET GAMSIZKAN, Nail ERSÖZ, AYŞE EKEN, Yusuf Sinan ŞİRİN, Müjdat BALKAN, Onur GENÇ

Sığır embriyolarının in vitro gelişiminde kültür medyumlarına katılan antioksidanların etkisi

Mustafa Numan BUCAK, Muharrem SATILMIŞ, SEDAT HAMDİ KIZIL, TAHİR KARAŞAHİN, NUMAN AKYOL

Estimation of optimum fattening period by cattles of Brown Swiss Hybrid (Fı) fattening

HASAN ÇİÇEK, YAVUZ CEVGER, MURAT TANDOĞAN, E. Hesna ŞAHİN

Macroscopic and light microscopic structure of fungiform papillae on the tongue of squirrels (Sciurus vulgaris)

Esin ÜNSALDI