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Evaluation of tissue factor activities and sialic acid levels in D-galactose induced aging model

Year 2014, Volume: 4 Issue: 1, 5 - 9, 25.04.2014

Abstract

Objective: The aims of this study are to evaluate the changes in tissue factor (TF) activities and sialic acid (SA) concentrations of D-galactose induced rat hepatic and renal tissues and compare with the naturally aged and the control groups. 

Methods: In this study Sprague-Dawley male rats (n=28, 20 weeks old) were used. The experiment and the control groups were organized as follows: 1) young male control group (n= 8, 20 weeks old). 2) naturally aged male group (n= 10) 3) D-Galactose induced ageing group (D-galactose injected (60 mg/kg/day) for 6 weeks, n= 8, 20-week-old). At the end of the treatment, the rats were sacrificed following an overnight fast, kidney and liver tissues were immediately collected for homogenization. TF activity and SA levels were measured by the methods of Quick and Warren respectively.

Results: SA levels of kidney decreased whereas TFa (TF activity) increased significantly in the D-galactose induced aging group when compared with the control and the naturally aged groups. SA levels of liver did not change significantly between the groups. TFa of liver increased significantly compared with the control group.

Conclusion: Increased TFa (TF activity) of kidney and liver and decreased SA levels of kidney in D-galactose induced aging model show that this model can be used in studies related with aging, thrombosis and haemostasis.

Key words: D-galactose, aging, tissue factor, sialic acid

References

  • Lai, Kent, Louis J. Elsas, and Klaas J. Wierenga. Galactose toxicity in animals. IUBMB life. 2009; 61(11): 1063-1074.
  • Song X, Bao M, Li D, Li YM. Advanced glycation in D-galactose induced mouse aging model. Mech Ageing Dev. 1999; 108(3): 2392
  • Traving C, and R. Schauer. Structure, function and metabolism of sialic acids. Cell Mol Life Sci. 1998; 54(12): 1330-1349.
  • Varki Ajit. Sialic acids in human health and disease. Inorg Chem. 2008; 14(8): 351-360.
  • Varki Nissi M, and Ajit Varki. Diversity in cell surface sialic acid presentations: implications for biology and disease. Lab invest. 2007; 87(9): 851-857.
  • Kökoğlu E, Sönmez H, Uslu E, Uslu I. Sialic acid levels in various types of cancer. Cancer Biochem Biophys. 1992; 13(1): 57-64.
  • Nemerson Y. Tissue factor and hemostasis. Blood. 1988; 71: 1-8.
  • Yarat A, Tunali T, Pisiriciler R, Akyuz S, Ipbuker A, Emekli N. Salivary thromboplastic activity in diabetics and healthy controls. Clin Oral Invest. 2004; 8(1): 36-39.
  • Emekli-Alturfan E, Kasikci E, Yarat A. Tissue factor activities of streptozotoc in induced diabetic rat tissues and the effect of peanut consumption. Diabetes Metab Res Rev. 2007; 23(8): 653-658.
  • Emekli-Alturfan E, Kasikci E, Yarat A. Peanutsim prove blood glutathione, HDL-cholesterol level and change tissue factor activity in rats fed a high-cholesterol diet. Eur J Nutr. 2007; 46(8): 476-82.
  • Emekli-Alturfan E, Kasikci E, Alturfan AA, Pisiriciler R, Yarat A. Effect of samplestorage on stability of salivary glutathione, lipid peroxidation levels, and tissue factor activity. J Clin Lab Anal. 2009; 23(2): 93-98.
  • Emekli-Alturfan E, Basar I, Malali E, Elemek E, Oktay S, Ayan F, Emekli N, Noyan U. Plasma tissue factor levels and salivary tissue factor activities of periodontitis patients with and without cardiovascular disease. Pathophysiol Haemost Thromb. 2010; 37(2-4): 77-81.
  • Emekli-Alturfan E, Kasikci E, Yarat A. Effects of oleic acid on the tissue factor activity, blood lipids, antioxidant and oxidant parameters of streptozotoc in induced diabetic rats fed a high-cholesterol diet. Med Chem Res. 2010; 19(8): 1011-1024.
  • Morrissey JH. Tissue factor and factor VII initiation of coagulation. In: Colman RW, Hirsh J, Marder VJ, Clowes AW, George JN, editors. Hemostasis and Thrombosis. Basic Principles and Clinical Practice. Philadelphia: Lippincott Williams & Wilkins; 2001. p. 89-102.
  • Lei M, Hua X, Xiao M, Ding J, Han Q, Hu G. Impairments of astrocytes are involved in the D-galactose induced brain aging. Biochem Biophys Res Commun. 2008; 369(4): 1082-1087.
  • Aydın S, Yanar K, Atukeren P, Dalo E, Sitar ME, Uslu E, Çakatay U. Comparison of oxidative stress biomarkers in renal tissues of d-galactose induced, naturally aged and young rats. Biogerontology. 2012; 13(3): 251-260.
  • Liu A, Ma Y, Zhu Z . Protective effect of selenoarginine aganist oxidative stress in D-galactose-induced aging mice. Biosci Biotechnol Biochem. 2009; 73(7): 1461-1464.
  • Warren L. The thiobarbituric acid assay of sialic acids. J Bio Chem. 1959; 234: 1971-5.
  • Ingram GIC, Hills M. Referance method for the one stage prothrombin time test on human blood. Thromb-Haemostas. 1976; 36: 237-238.
  • Zhang X, Li WB, Zhang BL. Biochemical changes in D-galactose induced subacute toxicity and mimetic aging in mice. Chinese J Pharm Toxicol. 1990; 4: 309-310.
  • Gong GQ, Xu FB, 1991. Study of aging model in mice. J China Pharm Univ. 1992; 22: 101-103.
  • Li WB, Wei F, Fan M, Zhang JL, Zhang BL, Ma XC, Yang WP, Wei W. Mimetic brain aging effect induced by D-galactose in mice. Chinese J Pharm Toxicol. 1995; 9: 93-95.
  • Newsome PN, Plevris JN, Nelson LJ, Hayes PC. Animal models of fulminant hepatic failure: a critical evaluation. Liver Transplantation. 2000; 6(1): 21-31.
  • Keppler D, Lesch R, Reutter W, Decker K. Experimental hepatitis induced by D-galactosamine. Exp Mol Pathol. 1968; 9(2): 279-290.
  • Wilkerson WR, Sane DC. Aging and thrombosis. Semin Thromb Hemost. 2002; 28(6): 555-568.
  • Muntané J, Montero JL, Marchal T, Perez-Seoane C, Lozano JM, Fraga E, et al. Effect of PGE1 on TNF-alpha status and hepatic D-galactosamine-induced apoptosis in rats. J Gastroenterol Hepatol. 1998; 13(2): 197-207.
  • Mehdi MM, Singh P, Rizvi SI. Erythrocyte sialic acid content during aging in humans: correlation with markers of oxidative stress. Dis Markers. 2012; 32(3): 179-186.
  • Gumus A, Balcan E. Determination of Glycoconjugate Residues of Erythrocytes at Different Age Groups of Rats. International Journal of Hematology and Oncology. 2000; 20(1): 6-13.
  • Greenwalt TJ, Steane EA. Quantitative haemagglutination. 5. Influence of in vivo aging and neuraminidase treatment on the M and N antigens of human red cells. Br J Haematol. 1973; 25: 217-226. Gattegno L, Bladier D, Cornillot P. Aging in vivo and neuraminidase treatment of rabbit erythrocytes: influenceon half-life as assessed by 51Cr labelling. Hoppe Seylers Z Physiol Chem. 1975; 356: 391-397.
  • Cakatay U, Aydın S, Atukeren P, Yanar K, E Sitar M, Dalo E, Uslu E. Increased Protein Oxidation and Loss of Protein-Bound Sialic Acid in Hepatic Tissues of D-galactose Induced Aged Rats. Current Aging Science. 2013; 6(2): 135-141.
  • Yamamoto K, Shimokawa T, Yi H, Isobe K, Kojima T, Loskutoff DJ, Saito H. Aging and obesity augment the stress-induced expression of tissue factor gene in the mouse. Blood. 2002; 100(12): 4011-4018.

D-galaktoz ile oluşturulmuş yaşlanma modelinde doku faktörü aktivitesinin ve sialik asit miktarının değerlendirilmesi

Year 2014, Volume: 4 Issue: 1, 5 - 9, 25.04.2014

Abstract

Amaç: Bu çalışmada D-galaktoz ile yaşlandırılmış, doğal yaşlı ve kontrol grubu sıçanların karaciğer ve renal dokularının doku faktörü (TF) aktivitelerinin ve inflamatuvar hastalıklar için değerli bir indikatör olan sialik asit (SA) miktarlarının ölçülmesi amaçlandı. 

Yöntemler: Çalışmada yirmi haftalık 28 adet Sprague-Dawley erkek rat kullanıldı. Gruplar; 1) genç kontrol grubu (n= 8), 2) doğal yaşlı erkek grup (n= 10), 3) 6 hafta süreyle 60 mg/kg/gün i.p. D-galaktoz enjekte edilen D-galaktoz ile yaşlandırılmış grup (n= 10) şeklinde oluşturuldu. İşlemler sonunda, ratlar bir gece aç bırakılarak sakrifiye edildi ve homojenizasyon için böbrek ve karaciğer dokuları toplandı. TF aktivitesi Quick metoduna, SA miktarı ise Warren’ın metoduna göre ölçüldü. 

Bulgular: D-galaktoz grubu böbrek dokusunda SA miktarı kontrol ve doğal yaşlı gruplara oranla anlamlı derecede azalmış, TF aktivitesi ise anlamlı derecede artmıştır. Karaciğer dokusu SA miktarında gruplar arasında anlamlı bir değişiklik gözlenmemiştir. Karaciğer TF aktivitesi ise D-galaktoz grubunda kontrol grubuna göre artmıştır. 

Sonuç: D-galaktoz ile oluşturulan yaşlanma modelinde böbrek ve karaciğer dokularında meydana gelen TF aktivitesi artışı ve böbrek SA seviyelerindeki azalma D-galaktozun yaşlanma ile ilgili tromboz/hemostaz çalışmalarında kullananılabileceğini göstermektedir.

 

Anahtar Kelimeler : D-galaktoz, yaşlanma, doku faktörü, sialik asit

References

  • Lai, Kent, Louis J. Elsas, and Klaas J. Wierenga. Galactose toxicity in animals. IUBMB life. 2009; 61(11): 1063-1074.
  • Song X, Bao M, Li D, Li YM. Advanced glycation in D-galactose induced mouse aging model. Mech Ageing Dev. 1999; 108(3): 2392
  • Traving C, and R. Schauer. Structure, function and metabolism of sialic acids. Cell Mol Life Sci. 1998; 54(12): 1330-1349.
  • Varki Ajit. Sialic acids in human health and disease. Inorg Chem. 2008; 14(8): 351-360.
  • Varki Nissi M, and Ajit Varki. Diversity in cell surface sialic acid presentations: implications for biology and disease. Lab invest. 2007; 87(9): 851-857.
  • Kökoğlu E, Sönmez H, Uslu E, Uslu I. Sialic acid levels in various types of cancer. Cancer Biochem Biophys. 1992; 13(1): 57-64.
  • Nemerson Y. Tissue factor and hemostasis. Blood. 1988; 71: 1-8.
  • Yarat A, Tunali T, Pisiriciler R, Akyuz S, Ipbuker A, Emekli N. Salivary thromboplastic activity in diabetics and healthy controls. Clin Oral Invest. 2004; 8(1): 36-39.
  • Emekli-Alturfan E, Kasikci E, Yarat A. Tissue factor activities of streptozotoc in induced diabetic rat tissues and the effect of peanut consumption. Diabetes Metab Res Rev. 2007; 23(8): 653-658.
  • Emekli-Alturfan E, Kasikci E, Yarat A. Peanutsim prove blood glutathione, HDL-cholesterol level and change tissue factor activity in rats fed a high-cholesterol diet. Eur J Nutr. 2007; 46(8): 476-82.
  • Emekli-Alturfan E, Kasikci E, Alturfan AA, Pisiriciler R, Yarat A. Effect of samplestorage on stability of salivary glutathione, lipid peroxidation levels, and tissue factor activity. J Clin Lab Anal. 2009; 23(2): 93-98.
  • Emekli-Alturfan E, Basar I, Malali E, Elemek E, Oktay S, Ayan F, Emekli N, Noyan U. Plasma tissue factor levels and salivary tissue factor activities of periodontitis patients with and without cardiovascular disease. Pathophysiol Haemost Thromb. 2010; 37(2-4): 77-81.
  • Emekli-Alturfan E, Kasikci E, Yarat A. Effects of oleic acid on the tissue factor activity, blood lipids, antioxidant and oxidant parameters of streptozotoc in induced diabetic rats fed a high-cholesterol diet. Med Chem Res. 2010; 19(8): 1011-1024.
  • Morrissey JH. Tissue factor and factor VII initiation of coagulation. In: Colman RW, Hirsh J, Marder VJ, Clowes AW, George JN, editors. Hemostasis and Thrombosis. Basic Principles and Clinical Practice. Philadelphia: Lippincott Williams & Wilkins; 2001. p. 89-102.
  • Lei M, Hua X, Xiao M, Ding J, Han Q, Hu G. Impairments of astrocytes are involved in the D-galactose induced brain aging. Biochem Biophys Res Commun. 2008; 369(4): 1082-1087.
  • Aydın S, Yanar K, Atukeren P, Dalo E, Sitar ME, Uslu E, Çakatay U. Comparison of oxidative stress biomarkers in renal tissues of d-galactose induced, naturally aged and young rats. Biogerontology. 2012; 13(3): 251-260.
  • Liu A, Ma Y, Zhu Z . Protective effect of selenoarginine aganist oxidative stress in D-galactose-induced aging mice. Biosci Biotechnol Biochem. 2009; 73(7): 1461-1464.
  • Warren L. The thiobarbituric acid assay of sialic acids. J Bio Chem. 1959; 234: 1971-5.
  • Ingram GIC, Hills M. Referance method for the one stage prothrombin time test on human blood. Thromb-Haemostas. 1976; 36: 237-238.
  • Zhang X, Li WB, Zhang BL. Biochemical changes in D-galactose induced subacute toxicity and mimetic aging in mice. Chinese J Pharm Toxicol. 1990; 4: 309-310.
  • Gong GQ, Xu FB, 1991. Study of aging model in mice. J China Pharm Univ. 1992; 22: 101-103.
  • Li WB, Wei F, Fan M, Zhang JL, Zhang BL, Ma XC, Yang WP, Wei W. Mimetic brain aging effect induced by D-galactose in mice. Chinese J Pharm Toxicol. 1995; 9: 93-95.
  • Newsome PN, Plevris JN, Nelson LJ, Hayes PC. Animal models of fulminant hepatic failure: a critical evaluation. Liver Transplantation. 2000; 6(1): 21-31.
  • Keppler D, Lesch R, Reutter W, Decker K. Experimental hepatitis induced by D-galactosamine. Exp Mol Pathol. 1968; 9(2): 279-290.
  • Wilkerson WR, Sane DC. Aging and thrombosis. Semin Thromb Hemost. 2002; 28(6): 555-568.
  • Muntané J, Montero JL, Marchal T, Perez-Seoane C, Lozano JM, Fraga E, et al. Effect of PGE1 on TNF-alpha status and hepatic D-galactosamine-induced apoptosis in rats. J Gastroenterol Hepatol. 1998; 13(2): 197-207.
  • Mehdi MM, Singh P, Rizvi SI. Erythrocyte sialic acid content during aging in humans: correlation with markers of oxidative stress. Dis Markers. 2012; 32(3): 179-186.
  • Gumus A, Balcan E. Determination of Glycoconjugate Residues of Erythrocytes at Different Age Groups of Rats. International Journal of Hematology and Oncology. 2000; 20(1): 6-13.
  • Greenwalt TJ, Steane EA. Quantitative haemagglutination. 5. Influence of in vivo aging and neuraminidase treatment on the M and N antigens of human red cells. Br J Haematol. 1973; 25: 217-226. Gattegno L, Bladier D, Cornillot P. Aging in vivo and neuraminidase treatment of rabbit erythrocytes: influenceon half-life as assessed by 51Cr labelling. Hoppe Seylers Z Physiol Chem. 1975; 356: 391-397.
  • Cakatay U, Aydın S, Atukeren P, Yanar K, E Sitar M, Dalo E, Uslu E. Increased Protein Oxidation and Loss of Protein-Bound Sialic Acid in Hepatic Tissues of D-galactose Induced Aged Rats. Current Aging Science. 2013; 6(2): 135-141.
  • Yamamoto K, Shimokawa T, Yi H, Isobe K, Kojima T, Loskutoff DJ, Saito H. Aging and obesity augment the stress-induced expression of tissue factor gene in the mouse. Blood. 2002; 100(12): 4011-4018.
There are 31 citations in total.

Details

Primary Language Turkish
Journal Section Articles
Authors

Ünsal Veli Üstündağ

Şehkar Oktay This is me

Ebru Emekli-alturfan This is me

Ahmet Ata Alturfan This is me

Karolin Yanar This is me

Murat Mengi This is me

Tamer Cebe This is me

Seval Aydın This is me

Ufuk Çakatay This is me

Publication Date April 25, 2014
Submission Date April 25, 2014
Published in Issue Year 2014 Volume: 4 Issue: 1

Cite

APA Üstündağ, Ü. V., Oktay, Ş., Emekli-alturfan, E., Alturfan, A. A., et al. (2014). D-galaktoz ile oluşturulmuş yaşlanma modelinde doku faktörü aktivitesinin ve sialik asit miktarının değerlendirilmesi. Clinical and Experimental Health Sciences, 4(1), 5-9.
AMA Üstündağ ÜV, Oktay Ş, Emekli-alturfan E, Alturfan AA, Yanar K, Mengi M, Cebe T, Aydın S, Çakatay U. D-galaktoz ile oluşturulmuş yaşlanma modelinde doku faktörü aktivitesinin ve sialik asit miktarının değerlendirilmesi. Clinical and Experimental Health Sciences. December 2014;4(1):5-9.
Chicago Üstündağ, Ünsal Veli, Şehkar Oktay, Ebru Emekli-alturfan, Ahmet Ata Alturfan, Karolin Yanar, Murat Mengi, Tamer Cebe, Seval Aydın, and Ufuk Çakatay. “D-Galaktoz Ile oluşturulmuş yaşlanma Modelinde Doku faktörü Aktivitesinin Ve Sialik Asit miktarının değerlendirilmesi”. Clinical and Experimental Health Sciences 4, no. 1 (December 2014): 5-9.
EndNote Üstündağ ÜV, Oktay Ş, Emekli-alturfan E, Alturfan AA, Yanar K, Mengi M, Cebe T, Aydın S, Çakatay U (December 1, 2014) D-galaktoz ile oluşturulmuş yaşlanma modelinde doku faktörü aktivitesinin ve sialik asit miktarının değerlendirilmesi. Clinical and Experimental Health Sciences 4 1 5–9.
IEEE Ü. V. Üstündağ, “D-galaktoz ile oluşturulmuş yaşlanma modelinde doku faktörü aktivitesinin ve sialik asit miktarının değerlendirilmesi”, Clinical and Experimental Health Sciences, vol. 4, no. 1, pp. 5–9, 2014.
ISNAD Üstündağ, Ünsal Veli et al. “D-Galaktoz Ile oluşturulmuş yaşlanma Modelinde Doku faktörü Aktivitesinin Ve Sialik Asit miktarının değerlendirilmesi”. Clinical and Experimental Health Sciences 4/1 (December 2014), 5-9.
JAMA Üstündağ ÜV, Oktay Ş, Emekli-alturfan E, Alturfan AA, Yanar K, Mengi M, Cebe T, Aydın S, Çakatay U. D-galaktoz ile oluşturulmuş yaşlanma modelinde doku faktörü aktivitesinin ve sialik asit miktarının değerlendirilmesi. Clinical and Experimental Health Sciences. 2014;4:5–9.
MLA Üstündağ, Ünsal Veli et al. “D-Galaktoz Ile oluşturulmuş yaşlanma Modelinde Doku faktörü Aktivitesinin Ve Sialik Asit miktarının değerlendirilmesi”. Clinical and Experimental Health Sciences, vol. 4, no. 1, 2014, pp. 5-9.
Vancouver Üstündağ ÜV, Oktay Ş, Emekli-alturfan E, Alturfan AA, Yanar K, Mengi M, Cebe T, Aydın S, Çakatay U. D-galaktoz ile oluşturulmuş yaşlanma modelinde doku faktörü aktivitesinin ve sialik asit miktarının değerlendirilmesi. Clinical and Experimental Health Sciences. 2014;4(1):5-9.

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