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Deneysel diyabetin karaciğer dokusunda oluşturduğu bazı değişiklikler üzerine çam yağının etkisi

Year 2014, Volume: 71 Issue: 3, 113 - 124, 01.09.2014

Abstract

Amaç: Bu çalışma; deneysel diyabet oluşturulan sıçanlarda çam yağının karaciğer dokusunda yağ asidi bileşimi, malondialdehit MDA , glutatyon GSH , total protein, ADEK vitaminleri, kolesterol ve bazı sterol parametreleri üzerinde etkisinin araştırılması için tasarlandı.Yöntem: Sıçanlar; kontrol K , streptozotosin STZ ve streptozotosin STZ + çam yağı ÇY olmak üzere üç grubu ayrıldı. STZ gruplarına intraperitoneal enjeksiyonla streptozotosin 45 mg/kg verilerek diyabet oluşturuldu. Çam yağı grubundaki sıçanlara haftada iki gün 1 mL/kg dozunda intraperitoneal enjeksiyonla çam yağı ve ayrıca 0,5 mL çam yağı 500 mL içme suyuna ilave edilerek verildi. Bu uygulamalar sekiz hafta boyunca sürdürüldü.Bulgular: Kontrol grubuna göre; STZ grubunun karaciğer dokusunda MDA ve total protein düzeyinin anlamlı bir şekilde p

References

  • Ugochukwu NH, Babady NE. Antioxidant effects of Gongronema latifolium in hepatocytes of rat models of non-insulin dependent diabetes mellitus. Fitoterapia, 2002; 73(7-8): 612-8.
  • Bellamkonda R, Rasineni K, Singareddy SR, Kasetti RB, Pasurla R, Chippada AR, et al. Antihyperglycemic and antioxidant activities of alcoholic extract of Commiphora mukul gum resin in streptozotocin induced diabetic rats. Pathophysiology, 2011; 18(4): 255-61.
  • Punithavathi VR, Anuthama R, Prince PS. Combined treatment with naringin and vitamin C ameliorates streptozotocin-induced diabetes in male Wistar rats. J Appl Toxicol, 2008; 28(6): 806-13.
  • Kızılaslan Ç, Sevgi E. Ethnobotanical uses of genus Pinus L. (Pinaceae) in Turkey. Indian J Tradit Know, 2013; 12(2): 209-20.
  • Demir E, Yılmaz Ö. Streptozotosin ile tip- 2 diyabet oluşturulan sıçanlarda çam yağının antihiperglisemik parametrelere etkisi. Marmara Üniv Fen Bil Derg, 2013; 25(3): 140-56. bazı biyokimyasal
  • Clark SP, Bollag WB, Westlund KN, Ma F, Falls G, Xie D, et al. Pine oil effects on chemical and thermal injury in mice and cultured mouse dorsal root ganglion neurons. Phytother Res, 2014; 28(2): 252-60.
  • Demir E, Yılmaz Ö. Streptozotosinin neden olduğu tip-1 diyabette çam yağının karaciğer ve böbrek dokusundaki bazı biyokimyasal parametrelere etkisi. Karaelmas Fen Müh Derg, 2014; 4(1): 43-51.
  • Biswas A, Chatterjee S, Chowdhury R, Sen S, Sarkar D, Chatterjee M, et al. Antidiabetic effect of seeds of Strychnos potatorum Linn. in a streptozotocin- induced model of diabetes. Acta Pol Pharm, 2012; 69(5): 939-43.
  • Dewanjee S, Das AK, Sahu R, Gangopadhyay M. Antidiabetic activity of Diospyros peregrina fruit: effect on hyperglycemia, hyperlipidemia and augmented oxidative stress in experimental type 2 diabetes. Food Chem Toxicol, 2009; 47(10): 2679-85.
  • Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem, 1979; 95(2): 351-8.
  • Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys, 1959; 82: 70-7.
  • Demir E, Yilmaz O, Ozsahin AD. The effect of some biochemical parameters in brain tissue of rats pine oil streptozotocin with experimental diabetes in rats. Int J Diabetes Res, 2013; 2(3): 39-44.
  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem, 1951; 193(1): 265-75.
  • Hara A, Radin NS. Lipid extraction of tissues with a lowtoxicity solvent. Anal Biochem, 1978; 90: 420-6.
  • Sánchez-Machado DI, López-Hernández J, Paseiro- Losada P. High-performance liquid chromatographic determination of alpha-tocopherol in macroalgae. J Chromatogr A, 2002; 976(1-2): 277-84.
  • López-Cervantes Ríos-Vázquez chromatography method for the simultaneous quantification of retinol, alpha-tocopherol, and cholesterol in shrimp waste hydrolysate. J Chromatogr A, 2006; 1105(1-2): 135-9. DI, liquid NJ. High-performance
  • Budin SB, Othman F, Louis SR, Bakar MA, Das S, Mohamed J. The effects of palm oil tocotrienol- rich fraction supplementation on biochemical parameters, oxidative stress and the vascular wall of streptozotocin-induced diabetic rats. Clinics (Sao Paulo), 2009; 64(3): 235-44.
  • Huang CS, Yin MC, Chiu LC. Antihyperglycemic and antioxidative potential of Psidium guajava fruit in streptozotocin-induced diabetic rats. Food Chem Toxicol, 2011; 49(9): 2189-95.
  • Peerapatdit T, Likidlilid A, Patchanans N, Somkasetrin A. Antioxidant status and lipid peroxidation end products in patients of type 1 diabetes mellitus. J Med Assoc Thai, 2006; 89 Suppl 5: 141-6.
  • Fenercioglu AK, Saler T, Genc E, Sabuncu H, Altuntas Y. The effects of polyphenol-containing antioxidants on oxidative stress and lipid peroxidation in type 2 diabetes mellitus without complications. J Endocrinol Invest, 2010; 33(2): 118-24.
  • Rohdewald PA. review of the French maritime pine bark extract (pycnogenol), a herbal medication with a diverse clinical pharmacology. Int J Clin Pharmacol Ther, 2002; 40(4): 158-68.
  • Parveen K, Ishrat T, Malik S, Kausar MA, Siddiqui WA. Modulatory effects of pycnogenol in a rat model of insulin-dependent diabetes mellitus: biochemical, histological, and immunohistochemical evidences. Protoplasma, 2013; 250(1): 347-60.
  • Maritim A, Dene BA, Sanders RA, Watkins JB 3rd. Effects of pycnogenol treatment on oxidative stress in streptozotocin-induced diabetic rats. J Biochem Mol Toxicol, 2003; 17(3): 193-9.
  • Kamuren ZT, McPeek CG, Sanders RA, Watkins JB 3rd. Effects of low-carbohydrate diet and pycnogenol treatment on retinal antioxidant enzymes in normal and diabetic rats. J Ocul Pharmacol Ther, 2006; 22(1): 10-8.
  • Jankyova S, Hlavackova L, Kralova E, Slazneva J, Drobna V, Zuzik P, et al. The evaluation of efficacy of pycnogenol® fractions on endothelial dysfunction. Acta Fac Pharm Univ Comen, 2013; LX(1): 7-14.
  • Das J, Vasan V, Sil PC. Taurine exerts hypoglycemic effect in alloxan-induced diabetic rats, improves insulin-mediated glucose transport signaling pathway in heart and ameliorates cardiac oxidative stress and apoptosis. Toxicol Appl Pharmacol, 2012; 258(2): 296-308.
  • Pari L, Venkateswaran S. Protective effect of Coccinia indica on changes in the fatty acid composition in streptozotocin induced diabetic rats. Pharmazie, 2003; 58(6): 409-12.
  • Douillet C, Bost M, Accominotti M, Borson-Chazot F, Ciavatti M. Effect of selenium and vitamin E supplements on tissue lipids, peroxides, and fatty acid distribution in experimental diabetes. Lipids, 1998; 33(4): 393-9.
  • Levant B, Ozias MK, Guilford BL, Wright DE. Streptozotocin-induced attenuates the effects of a high-fat diet on liver and brain fatty acid composition in mice. Lipids, 2013; 48(9): 939-48. diabetes partially
  • Celik S, Baydaş G, Yilmaz O. Influence of vitamin E on the levels of fatty acids and MDA in some tissues of diabetic rats. Cell Biochem Funct, 2002; 20(1): 67-71.
  • Ntambi JM. Regulation of stearoyl-CoA desaturase by polyunsaturated fatty acids and cholesterol. J Lipid Res, 1999; 40(9): 1549-58.
  • Brenner RR, Bernasconi AM, Garda HA. Effect of experimental diabetes on the fatty acid composition, molecular species of phosphatidyl- choline and physical properties of hepatic microsomal membranes. Prostaglandins Leukot Essent Fatty Acids, 2000; 63(3): 167-76.
  • Nakamura MT, Nara TY. Structure, function, and dietary regulation of delta6, delta5, and delta9 desaturases. Annu Rev Nutr, 2004; 24: 345-76.
  • Shimano H. Sterol regulatory element-binding proteins (SREBPs): transcriptional regulators of lipid synthetic genes. Prog Lipid Res, 2001; 40(6): 439-52.
  • Espenshade PJ. SREBPs: transcription factors. J Cell Sci, 2006; 119(Pt 6): 973-6. sterol-regulated
  • Mimouni V, Poisson JP. Altered desaturase activities and fatty acid composition in liver microsomes of spontaneously diabetic Wistar BB rat. Biochim Biophys Acta, 1992; 1123(3): 296-302.
  • Etzl RP, Vrekoussis T, Kuhn C, Schulze S, Pöschl JM, Makrigiannakis A, et al. Oxidative stress stimulates α-tocopherol transfer protein in human trophoblast tumor cells BeWo. J Perinat Med, 2012; 40(4): 373-8.
  • Miyazaki H, Takitani K, Koh M, Takaya R, Yoden A, Tamai H. α-Tocopherol status and expression of α-tocopherol transfer protein in type 2 diabetic Goto-Kakizaki rats. J Nutr Sci Vitaminol (Tokyo), 2013; 59(1): 64-8.
  • Brown MS, Goldstein JL. The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor. Cell, 1997; 89(3): 331-40.
  • Scoggan KA, Gruber H, Chen Q, Plouffe LJ, Lefebvre JM, Wang B, et al. Increased incorporation of dietary plant sterols and cholesterol correlates with decreased expression of hepatic and intestinal Abcg5 and Abcg8 in diabetic BB rats. J Nutr Biochem, 2009; 20(3): 177-86.
  • Tuitoek PJ, Ziari S, Tsin AT, Rajotte RV, Suh M, Basu TK. Streptozotocin-induced diabetes in rats is associated with impaired metabolic availability of vitamin A (retinol). Br J Nutr, 1996; 75(4): 615-22.

The effect of pine oil on the some alterations in liver tissue of experimental diabetes

Year 2014, Volume: 71 Issue: 3, 113 - 124, 01.09.2014

Abstract

Objective: The present study was designed to evaluate the impact of pine oil on MDA malondialdehyde , GSH glutathione , total protein, fatty acid composition, ADEK vitamins, cholesterol and some sterols parameters in liver tissue of experimental diabetes in rats.Method: The rats were divided into three groups: control C streptozotocin STZ , streptozotocin STZ + pine oil PO groups. Diabetes induced in rats by a single intraperitoneal injection of streptozotocin 45 mg/kg . 1 mL/kg dose pine oil was intraperitoneally injected twice in a week to the streptozotocin STZ + pine oil PO , and additionally 0.5 mL /500 mL dose of pine oil was added to drinking water of this group. The experiment continued for eight weeks.Results: It was observed that MDA and total protein levels were significantly increased p

References

  • Ugochukwu NH, Babady NE. Antioxidant effects of Gongronema latifolium in hepatocytes of rat models of non-insulin dependent diabetes mellitus. Fitoterapia, 2002; 73(7-8): 612-8.
  • Bellamkonda R, Rasineni K, Singareddy SR, Kasetti RB, Pasurla R, Chippada AR, et al. Antihyperglycemic and antioxidant activities of alcoholic extract of Commiphora mukul gum resin in streptozotocin induced diabetic rats. Pathophysiology, 2011; 18(4): 255-61.
  • Punithavathi VR, Anuthama R, Prince PS. Combined treatment with naringin and vitamin C ameliorates streptozotocin-induced diabetes in male Wistar rats. J Appl Toxicol, 2008; 28(6): 806-13.
  • Kızılaslan Ç, Sevgi E. Ethnobotanical uses of genus Pinus L. (Pinaceae) in Turkey. Indian J Tradit Know, 2013; 12(2): 209-20.
  • Demir E, Yılmaz Ö. Streptozotosin ile tip- 2 diyabet oluşturulan sıçanlarda çam yağının antihiperglisemik parametrelere etkisi. Marmara Üniv Fen Bil Derg, 2013; 25(3): 140-56. bazı biyokimyasal
  • Clark SP, Bollag WB, Westlund KN, Ma F, Falls G, Xie D, et al. Pine oil effects on chemical and thermal injury in mice and cultured mouse dorsal root ganglion neurons. Phytother Res, 2014; 28(2): 252-60.
  • Demir E, Yılmaz Ö. Streptozotosinin neden olduğu tip-1 diyabette çam yağının karaciğer ve böbrek dokusundaki bazı biyokimyasal parametrelere etkisi. Karaelmas Fen Müh Derg, 2014; 4(1): 43-51.
  • Biswas A, Chatterjee S, Chowdhury R, Sen S, Sarkar D, Chatterjee M, et al. Antidiabetic effect of seeds of Strychnos potatorum Linn. in a streptozotocin- induced model of diabetes. Acta Pol Pharm, 2012; 69(5): 939-43.
  • Dewanjee S, Das AK, Sahu R, Gangopadhyay M. Antidiabetic activity of Diospyros peregrina fruit: effect on hyperglycemia, hyperlipidemia and augmented oxidative stress in experimental type 2 diabetes. Food Chem Toxicol, 2009; 47(10): 2679-85.
  • Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem, 1979; 95(2): 351-8.
  • Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys, 1959; 82: 70-7.
  • Demir E, Yilmaz O, Ozsahin AD. The effect of some biochemical parameters in brain tissue of rats pine oil streptozotocin with experimental diabetes in rats. Int J Diabetes Res, 2013; 2(3): 39-44.
  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. Protein measurement with the folin phenol reagent. J Biol Chem, 1951; 193(1): 265-75.
  • Hara A, Radin NS. Lipid extraction of tissues with a lowtoxicity solvent. Anal Biochem, 1978; 90: 420-6.
  • Sánchez-Machado DI, López-Hernández J, Paseiro- Losada P. High-performance liquid chromatographic determination of alpha-tocopherol in macroalgae. J Chromatogr A, 2002; 976(1-2): 277-84.
  • López-Cervantes Ríos-Vázquez chromatography method for the simultaneous quantification of retinol, alpha-tocopherol, and cholesterol in shrimp waste hydrolysate. J Chromatogr A, 2006; 1105(1-2): 135-9. DI, liquid NJ. High-performance
  • Budin SB, Othman F, Louis SR, Bakar MA, Das S, Mohamed J. The effects of palm oil tocotrienol- rich fraction supplementation on biochemical parameters, oxidative stress and the vascular wall of streptozotocin-induced diabetic rats. Clinics (Sao Paulo), 2009; 64(3): 235-44.
  • Huang CS, Yin MC, Chiu LC. Antihyperglycemic and antioxidative potential of Psidium guajava fruit in streptozotocin-induced diabetic rats. Food Chem Toxicol, 2011; 49(9): 2189-95.
  • Peerapatdit T, Likidlilid A, Patchanans N, Somkasetrin A. Antioxidant status and lipid peroxidation end products in patients of type 1 diabetes mellitus. J Med Assoc Thai, 2006; 89 Suppl 5: 141-6.
  • Fenercioglu AK, Saler T, Genc E, Sabuncu H, Altuntas Y. The effects of polyphenol-containing antioxidants on oxidative stress and lipid peroxidation in type 2 diabetes mellitus without complications. J Endocrinol Invest, 2010; 33(2): 118-24.
  • Rohdewald PA. review of the French maritime pine bark extract (pycnogenol), a herbal medication with a diverse clinical pharmacology. Int J Clin Pharmacol Ther, 2002; 40(4): 158-68.
  • Parveen K, Ishrat T, Malik S, Kausar MA, Siddiqui WA. Modulatory effects of pycnogenol in a rat model of insulin-dependent diabetes mellitus: biochemical, histological, and immunohistochemical evidences. Protoplasma, 2013; 250(1): 347-60.
  • Maritim A, Dene BA, Sanders RA, Watkins JB 3rd. Effects of pycnogenol treatment on oxidative stress in streptozotocin-induced diabetic rats. J Biochem Mol Toxicol, 2003; 17(3): 193-9.
  • Kamuren ZT, McPeek CG, Sanders RA, Watkins JB 3rd. Effects of low-carbohydrate diet and pycnogenol treatment on retinal antioxidant enzymes in normal and diabetic rats. J Ocul Pharmacol Ther, 2006; 22(1): 10-8.
  • Jankyova S, Hlavackova L, Kralova E, Slazneva J, Drobna V, Zuzik P, et al. The evaluation of efficacy of pycnogenol® fractions on endothelial dysfunction. Acta Fac Pharm Univ Comen, 2013; LX(1): 7-14.
  • Das J, Vasan V, Sil PC. Taurine exerts hypoglycemic effect in alloxan-induced diabetic rats, improves insulin-mediated glucose transport signaling pathway in heart and ameliorates cardiac oxidative stress and apoptosis. Toxicol Appl Pharmacol, 2012; 258(2): 296-308.
  • Pari L, Venkateswaran S. Protective effect of Coccinia indica on changes in the fatty acid composition in streptozotocin induced diabetic rats. Pharmazie, 2003; 58(6): 409-12.
  • Douillet C, Bost M, Accominotti M, Borson-Chazot F, Ciavatti M. Effect of selenium and vitamin E supplements on tissue lipids, peroxides, and fatty acid distribution in experimental diabetes. Lipids, 1998; 33(4): 393-9.
  • Levant B, Ozias MK, Guilford BL, Wright DE. Streptozotocin-induced attenuates the effects of a high-fat diet on liver and brain fatty acid composition in mice. Lipids, 2013; 48(9): 939-48. diabetes partially
  • Celik S, Baydaş G, Yilmaz O. Influence of vitamin E on the levels of fatty acids and MDA in some tissues of diabetic rats. Cell Biochem Funct, 2002; 20(1): 67-71.
  • Ntambi JM. Regulation of stearoyl-CoA desaturase by polyunsaturated fatty acids and cholesterol. J Lipid Res, 1999; 40(9): 1549-58.
  • Brenner RR, Bernasconi AM, Garda HA. Effect of experimental diabetes on the fatty acid composition, molecular species of phosphatidyl- choline and physical properties of hepatic microsomal membranes. Prostaglandins Leukot Essent Fatty Acids, 2000; 63(3): 167-76.
  • Nakamura MT, Nara TY. Structure, function, and dietary regulation of delta6, delta5, and delta9 desaturases. Annu Rev Nutr, 2004; 24: 345-76.
  • Shimano H. Sterol regulatory element-binding proteins (SREBPs): transcriptional regulators of lipid synthetic genes. Prog Lipid Res, 2001; 40(6): 439-52.
  • Espenshade PJ. SREBPs: transcription factors. J Cell Sci, 2006; 119(Pt 6): 973-6. sterol-regulated
  • Mimouni V, Poisson JP. Altered desaturase activities and fatty acid composition in liver microsomes of spontaneously diabetic Wistar BB rat. Biochim Biophys Acta, 1992; 1123(3): 296-302.
  • Etzl RP, Vrekoussis T, Kuhn C, Schulze S, Pöschl JM, Makrigiannakis A, et al. Oxidative stress stimulates α-tocopherol transfer protein in human trophoblast tumor cells BeWo. J Perinat Med, 2012; 40(4): 373-8.
  • Miyazaki H, Takitani K, Koh M, Takaya R, Yoden A, Tamai H. α-Tocopherol status and expression of α-tocopherol transfer protein in type 2 diabetic Goto-Kakizaki rats. J Nutr Sci Vitaminol (Tokyo), 2013; 59(1): 64-8.
  • Brown MS, Goldstein JL. The SREBP pathway: regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor. Cell, 1997; 89(3): 331-40.
  • Scoggan KA, Gruber H, Chen Q, Plouffe LJ, Lefebvre JM, Wang B, et al. Increased incorporation of dietary plant sterols and cholesterol correlates with decreased expression of hepatic and intestinal Abcg5 and Abcg8 in diabetic BB rats. J Nutr Biochem, 2009; 20(3): 177-86.
  • Tuitoek PJ, Ziari S, Tsin AT, Rajotte RV, Suh M, Basu TK. Streptozotocin-induced diabetes in rats is associated with impaired metabolic availability of vitamin A (retinol). Br J Nutr, 1996; 75(4): 615-22.
There are 41 citations in total.

Details

Primary Language Turkish
Journal Section Research Article
Authors

Ersin Demir This is me

Ökkeş Yılmaz This is me

Publication Date September 1, 2014
Published in Issue Year 2014 Volume: 71 Issue: 3

Cite

APA Demir, E., & Yılmaz, Ö. (2014). Deneysel diyabetin karaciğer dokusunda oluşturduğu bazı değişiklikler üzerine çam yağının etkisi. Türk Hijyen Ve Deneysel Biyoloji Dergisi, 71(3), 113-124.
AMA Demir E, Yılmaz Ö. Deneysel diyabetin karaciğer dokusunda oluşturduğu bazı değişiklikler üzerine çam yağının etkisi. Turk Hij Den Biyol Derg. September 2014;71(3):113-124.
Chicago Demir, Ersin, and Ökkeş Yılmaz. “Deneysel Diyabetin karaciğer Dokusunda oluşturduğu Bazı değişiklikler üzerine çam yağının Etkisi”. Türk Hijyen Ve Deneysel Biyoloji Dergisi 71, no. 3 (September 2014): 113-24.
EndNote Demir E, Yılmaz Ö (September 1, 2014) Deneysel diyabetin karaciğer dokusunda oluşturduğu bazı değişiklikler üzerine çam yağının etkisi. Türk Hijyen ve Deneysel Biyoloji Dergisi 71 3 113–124.
IEEE E. Demir and Ö. Yılmaz, “Deneysel diyabetin karaciğer dokusunda oluşturduğu bazı değişiklikler üzerine çam yağının etkisi”, Turk Hij Den Biyol Derg, vol. 71, no. 3, pp. 113–124, 2014.
ISNAD Demir, Ersin - Yılmaz, Ökkeş. “Deneysel Diyabetin karaciğer Dokusunda oluşturduğu Bazı değişiklikler üzerine çam yağının Etkisi”. Türk Hijyen ve Deneysel Biyoloji Dergisi 71/3 (September 2014), 113-124.
JAMA Demir E, Yılmaz Ö. Deneysel diyabetin karaciğer dokusunda oluşturduğu bazı değişiklikler üzerine çam yağının etkisi. Turk Hij Den Biyol Derg. 2014;71:113–124.
MLA Demir, Ersin and Ökkeş Yılmaz. “Deneysel Diyabetin karaciğer Dokusunda oluşturduğu Bazı değişiklikler üzerine çam yağının Etkisi”. Türk Hijyen Ve Deneysel Biyoloji Dergisi, vol. 71, no. 3, 2014, pp. 113-24.
Vancouver Demir E, Yılmaz Ö. Deneysel diyabetin karaciğer dokusunda oluşturduğu bazı değişiklikler üzerine çam yağının etkisi. Turk Hij Den Biyol Derg. 2014;71(3):113-24.