54
Views
0
CrossRef citations to date
0
Altmetric
Original Articles

The Efficacy of Carvacrol on Renal Damage in Rats with Acute Pancreatitis

, , , , &
Pages 847-858 | Received 16 Feb 2014, Accepted 24 May 2014, Published online: 23 Dec 2014

References

  • Naumovski-Mihalic, S. (2009). Treatment of acute pancreatitis. Lijec Vjesnik. 131: 15–18.
  • Chen, L., Lu, G., Zhou, Q., Zhan, Q. (2013). Evaluation of the BISAP Score in Predicting Severity and Prognoses of Acute Pancreatitis in Chinese Patients. International Surgery. 98: 6–12. doi: 10.9738/0020-8868-98.1.6
  • Mohmand, H., Goldfarb, S. (2011). Renal dysfunction associated with intra-abdominal hypertension and the abdominal compartment syndrome. Journal of the American Society of Nephrology. 22: 615–621. doi: 10.1681/ASN.2010121222
  • Lin, H.Y., Lai, J.I., Lai, Y.C., Lin, P.C., Chang, S.C., Tang, G.J. (2011). Acute renal failure in severe pancreatitis: A population-based study. Upsala Journal of Medical Sciences. 116: 155–159 doi: 10.3109/03009734.2010.547636
  • Blundell, R., Adam, F. (2013). Haemolytic anaemia and acute pancreatitis associated with zinc toxicosis in a dog. Veterinary Record. 172: 17–25. doi: 10.1136/vr.100376
  • Zhou, M., Chen, B., Sun, H., Deng, Z., Andersson, R., Zhang, Q. (2011). The protective effects of Lipoxin A4 during the early phase of severe acute pancreatitis in rats. Scandinavian Journal of Gastroenterology. 46: 211–219. doi: 10.3109/00365521.2010.525715
  • Wen, Z., Liao, Q., Hu, Y., Liu, S., You, L., Zhao, Y. (2013). Human adipose-derived stromal/stem cells: A novel approach to inhibiting acute pancreatitis. Medical Hypotheses. 5: 598–600. doi: 10.1016/j.mehy.2013.01.034
  • Dababneh, B.F. (2007). Antimicrobial activity and genetic diversity of Thymus species on pathogenic microorganisms. Journal of Food Agrýculture and Environment. 5: 158–162.
  • Adorjan, B., Buchbauer, G. (2010). Biological properties of essential oils: an updated review. Flavour and Fragrance Journal. 25: 407–426. doi: 10.1002/ffj.2024
  • Elhabazi, K., Dicko, A., Desor, F., Dalal, A., Younos, C., Soulimani, R. (2006). Preliminary study on immunological and behavioural effects of Thymus broussonetii Boiss., an endemic species in Morocco. Journal of Ethnopharmacology. 103: 413–419. doi: 10.1016/j.jep.2005.08.034
  • Beena. Kumar, D., Rawat, D.S. (2013). Synthesis and antioxidant activity of thymol and carvacrol based Schiff bases. Bioorganic & Medicinal Chemistry Letters. 23: 641–645. doi: 10.1016/j.bmcl.2012.12.001
  • Yu, J., Deng, W., Wang, W., Ding, Y., Jin, H., Chen, C., Chen, X., Xiong, X., Xu, S. (2012). Inhibition of poly (ADP-ribose) polymerase attenuates acute kidney injury in sodium taurocholate-induced acute pancreatitis in rats. Pancreas. 41: 1299–1305. doi: 10.1097/MPA.0b013e318252dbc3
  • National Research Council (US). (1999). International Committee of the Institute for Laboratory Animal Research. Microbial Status and Genetic Evaluation of Mice and Rats. Proceedings of the 1999 US/Japan Conference. Washington (DC): National Academies Press (US); 2000.p.166. ISBN-10: 0-309-07195-X.
  • Hagiwara, S., Iwaska, H., Uchida, T., Hasegawa, A., Asai, N., Noguchi, T. (2009). Danaparoid sodium prevents cerulein-induced acute pancreatitis in rats. Shock. 32: 94–99. doi: 10.1097/SHK.0b013e31818ec2c2
  • Misra, H.P., Fridovich, I. (1972). The role of superoxide anion in the auto oxidation of epin-ephrine and a simple assay for superoxide dismutase. J. Biol. Chem. 247: 3170–3175.
  • Beers, R.F., Sizer, I.W. (1952). A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. Journal of Biological Chemistry. 195: 133–140.
  • Rotruck, J.T., Pope, A.L., Ganther, H.E., Swanson, A.B., Hafeman, D.G., Hoekstra, W.G. (1973). Selenium: biochemical role as a component of glutathione peroxidase. Science. 179: 588–590. doi: 10.1126/science.179.4073.588
  • Ohkawa, H., Ohishi, N., Yagi, K. (1979). Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry. 95: 351–358. doi: 10.1016/0003-2697(79)90738-3
  • Teixeira, R.B., Kelly, J., Alpert, H., Pardo, V., Vaamonde, C.A. (1982). Complete protection from gentamicin-induced acute renal failure in the diabetes mellitus rat. Kidney International. 21: 600–612. doi: 10.1038/ki.1982.67
  • Kamei, K., Yasuda, T., Ueda, T., Qiang, F., Takeyama, Y., Shiozaki, H. (2010). Role of triggering receptor expressed on myeloid cells-1 in experimental severe acute pancreatitis. Journal of Hepatobiliary Pancreatic Science. 17: 305–312. doi: 10.1007/s00534-009-0191-6
  • Halliwell, B. (1994). Free radicals, antioxidant and human disease: Curiosity, cause or consequence?. Lancet. 344: 721–724. doi: 10.1016/S0140-6736(94)92211-X
  • Bhatia, M., Brady, M., Shokuhi, S., Christmas, S., Neoptolemos, J.P., Slavin, J. (2000). Inflammatory mediators in acute pancreatitis. Journal of Pathology. 190: 117–125. doi: 10.1002/(SICI)1096-9896(200002)190:2<117::AID-PATH494>3.0.CO;2-K
  • Okamura, D., Starr, ME., Lee, E.Y., Stromberg, A.J., Evers, B.M., Saito, H. (2012). Age-dependent vulnerability to experimental acute pancreatitis is associated with increased systemic inflammation and thrombosis. Aging Cell. 11: 760–769. doi: 10.1111/j.1474-9726.2012.00841.x
  • Assaly, R., Olson, D., Hammersley, J., Fan, P.S., Liu, J., Shapiro, J.I., Kahaleh, M.B. (2001). Initial evidence of endothelial cell apoptosis as a mechanism of systemic capillary leak syndrome. Chest. 120: 1301–1308. doi: 10.1378/chest.120.4.1301
  • Grigor'eva, I.N., Romanova, T.I., Ragino, I.I. (2011). Lipid peroxidation in patients with acute and chronic pancreatitis. Experimental and Clinical Gastroenterology. 7: 24–27.
  • Zhang, D.Q., Zhu, J.H. (2012). Experimental studies of effects of hydrogen-rich saline in rats with severe acute pancreatitis. Zhonghua Yi Xue Za Zhi. 92: 2436–2440.
  • Ienaga, K., Park, C.H., Yokozawa, T. (2012). Protective effect of an intrinsic antioxidant, HMH (5-hydroxy-1-methylhydantoin; NZ-419), against cellular damage of kidney tubules. Experimental and Toxicologic Pathology in press, doi: 10.1016/j.etp.2012.05.001.
  • Rahman, S.H., Ammori, B.J., Holmfield, J., Larvin, M., McMahon, M.J. (2003). Intestinal hypoperfusion contributes to gut barrier failure in severe acute pancreatitis. Journal of Gastroýntestýnal Surgery. 7: 26–36. doi: 10.1016/S1091-255X(02)00090-2
  • Reiner, G.N., Delgado-Marín, L., Olguín, N., Sánchez-Redondo, S., Sánchez-Borzone, M., Rodríguez-Farré, E., Suñol, C., García, D.A. (2013). Gabaergic Pharmacological Activity of Propofol Related Compounds as Possible Enhancers of General Anesthetics and Interaction with Membranes. Cell Býochemýstry and Býophysýcs in press, doý: 10.1007/s12013-013-9537-4.
  • Aeschbach, R., Löliger, J., Scott, B.C., Murcia, A., Butler, J., Halliwell, B., Aruoma, O.I. (1994). Antioxidant actions of thymol, carvacrol, 6-gingerol, zingerone and hydroxyltyrosol. Food and Chemical Toxicology. 32: 31–36. doi: 10.1016/0278-6915(84)90033-4
  • Schulz, H.U., Niederau, C. (1994). Oxidative stress-induced changes in pancreatic acinar cells: Insights from in vitro studies. Hepatogastroenterology. 41: 309–312.
  • Willemer, S., Elsässer, H.P., Adler, G. (1992). Hormone-induced pancreatitis. European Surgical Research. 24: 29–39. doi: 10.1159/000129237
  • Snook, J.H., Li, J., Helmke, B.P., Guilford, W.H. (2008). Peroxynitrite inhibits myofibrillar protein function in an in vitro assay of motility. Free Radical Biology and Medicine. 44: 14–23. doi: 10.1016/j.freeradbiomed.2007.09.004
  • Iaremchuk, O.Z., Posokhov,a K.A. (2011). The liver and kidneys biochemical indices at the experimental pancreatitis in case of the administration of nitric oxide synthesis modulators and recombinant superoxide dismutase. Ukrainski- Biokhimicheski- Zhurnal. 83: 57–66.
  • Luan, Z.G., Zhang, J., Yin, X.H., Ma, X.C., Guo, R.X. (2013). Ethyl pyruvate significantly inhibits tumour necrosis factor-á, interleukin-1â and high mobility group box 1 releasing and attenuates sodium taurocholate-induced severe acute pancreatitis associated with acute lung injury. Clinical and Experimental Immunology. 172: 417–426. doi: 10.1111/cei.12062
  • Petrov, M.S. (2010). Therapeutic implications of oxidative stress in acute and chronic pancreatitis. Current Opinion in Clinical Nutrition & Metabolic Care. 13: 562–568. doi: 10.1097/MCO.0b013e32833b64b9
  • Suppiah, A., Malde, D., Arab, T., Hamed, M., Allgar, V., Smith, A.M., Morris-Stiff, G. (2013). The Prognostic Value of the Neutrophil-Lymphocyte Ratio (NLR) in Acute Pancreatitis: Identi- fication of an Optimal NLR. Journal of Gastrointestinal Surgury. 17: 675–681. doi: 10.1007/s11605-012-2121-1
  • Zhao, G., Zhang, J.G., Wu, H.S., Tao, J., Qin, Q., Deng, S.C., Liu, Y., Liu, L., Wang, B., Tian, K., Li, X., Zhu, S., Wang, C.Y. (2013). Effects of different resuscitation fluid on severe acute pancreatitis. World Journal of Gastroenterology. 19: 2044–2052. doi: 10.3748/wjg.v19.i13.2044
  • Mifkovic, A., Skultety, J., Sykora, P., Prochotsky, A., Okolicany, R. (2013). Intra-abdominal hypertension and acute pancreatitis. Bratýslava Medical Journal-Bratýslavske Lekarske Lýsty. 114: 166–171. doi: 10.4149/BLL_2013_036
  • Kes, P., Vuciceviæ, Z., Ratkoviæ-Gusiæ, I. (1996). A. Fotivec Acute renal failure complicating severe acute pancreatitis. Renal Failure. 187: 621–628. doi: 10.3109/08860229609047686
  • Shields, C.J., Winter, D.C., Redmond, H.P. (2002). Lung injury in acute pancreatitis: mechanisms, prevention, and therapy. Current Opinion in Critical Care. 8: 158–163. doi: 10.1097/00075198-200204000-00012
  • Muñoz-Casares, F.C., Padillo, F.J., Briceño, J., Collado, J.A., Muñoz-Castañeda, J.R., Ortega, R., Cruz, A., Túnez, I., Montilla, P., Pera, C., Muntané, J. (2006). Melatonin reduces apoptosis and necrosis induced by ischemia/reperfusion injury of the pancreas. Journal of Pineal Research. 40: 195–203. doi: 10.1111/j.1600-079X.2005.00291.x
  • Esmaeili, A. (2013). Biological activities and chemical composition of the stems and roots of Helichrysum oligocephalum DC grown in Iran. Pakistan Journal of Pharmacological Science. 26: 599–604.
  • Silva, F.V., Guimarães, A.G., Silva, E.R., Sousa-Neto, B.P., Machado, F.D., Quintans-Júnior, L.J., Arcanjo, D.D., Oliveira, F.A., Oliveira, R.C. (2012). Anti-inflammatory and anti-ulcer activities of carvacrol, a monoterpene present in the essential oil of oregano. Journal of Medicinal Food. 15: 984–991. doi: 10.1089/jmf.2012.0102
  • Hotta, M., Nakata, R., Katsukawa, M., Hori, K., Takahashi, S., Inoue, H. (2010). Carvacrol, a component of thyme oil, activates PPARalpha and gamma and suppresses COX-2 expression. Journal Lipid Research. 51: 132–139. doi: 10.1194/jlr.M900255-JLR200
  • Fabian, E., Pölöskey, P., Kósa, L., Elmadfa, I., Réthy, L.A. (2013). Nutritional supplements and plasma antioxidants in childhood asthma. The Central European Journal of Medicine in press, doi: 10.1007/s00508-013-0359-6.
  • Aristatile, B., Al-Numair, K.S., Veeramani, C., Pugalendi, K.V. (2009). Effect of carvacrol on hepatic marker enzymes and antioxidant status in D-galactosamine-induced hepatotoxicity in rats. Fundamental & Clýnýcal Pharmacology. 23: 757–765. doi: 10.1111/j.1472-8206.2009.00721.x
  • Saei-Dehkordi, S.S., Tajik, H., Moradi, M., Khalighi-Sigaroodi, F. (2010). Chemical composition of essential oils in Zataria multiflora Boiss. from different parts of Iran and their radical scavenging and antimicrobial activity. Food and Chemical Toxicology. 48: 1562–1567. doi: 10.1016/j.fct.2010.03.025
  • Oke, F., Aslim, B., Ozturk, S., Altundag, S. (2009). Essential oil composition, antimicrobial and antioxidant activities of Satureja cuneifolia Ten. Food Chemistry. 112: 874–879. doi: 10.1016/j.foodchem.2008.06.061
  • Bousta, D., Soulimani, R., Jarmouni, S., Belon, P., Falla, J., Froment, N., Younos, C. (2001). Neurotropic, immunological and gastric effects of low doses of Atropa Belladona L., Gelsemium sempervirens L. and Poumon histamine in stressed mice. Journal of Ethnopharmacology. 74: 205–215. doi: 10.1016/S0378-8741(00)00346-9
  • Thamilselvan, S., Byer, K.J., Hackett, R.L., Khan, S.R. (2000). Free radical scavengers, catalase and superoxide dismutase provide protection from oxalate-associated injury to LLC-PK1 and MDCK cells. Journal of Urology. 164: 224–229. doi: 10.1016/S0022-5347(05)67499-X
  • Romeu, M., Mulero, M., Giralt, M., Folch, J., Nogués, M.R., Torres, A., Fortuño, A., Sureda, F.X., Cabré, M., Paternáin, J.L., Mallol, J. (2002). Parameters related to oxygen free radicals in erythrocytes, plasma and epidermis of the hairless rat. Life Sciences. 71: 1739–1749. doi: 10.1016/S0024-3205(02)01946-X
  • Zhou, X., Yao, Y. (2013). Unexpected Nephrotoxicity in Male Ablactated Rats Induced by Cordyceps militaris: The Involvement of Oxidative Changes. Evid Based Complement Alternative Medicine in press, doi: 10.1155/2013/786528.
  • Boskabady, M.H., Jalali, S. (2013). Effect of carvacrol on tracheal responsiveness, inflammatory mediators, total and differential WBC count in blood of sensitized guinea pigs. Exp Biol Med (Maywood). 238: 200–208. doi: 10.1177/1535370212474604
  • Jayakumar, S., Madankumar, A., Asokkumar, S., Raghunandhakumar, S., Gokula, D.K., Kamaraj, S., Divya, M.G., Devaki, T. (2012). Potential preventive effect of carvacrol against diethylnitrosamine-induced hepatocellular carcinoma in rats. Molecular and cellular býochem ýstry. 360: 51–60. doi: 10.1007/s11010-011-1043-7
  • Le Campion, E.R., Jukemura, J., Coelho, A.M., Patzina, R., Carneiro D'Albuquerque, L.A. (2012). Effects of intravenous administration of pentoxifylline in pancreatic ischaemia-reperfusion injury. HPB (Oxford). doi: 10.1111/hpb.12013.
  • Undeðer, U., Baþaran, A., Degen, G.H., Baþaran, N. (2009). Antioxidant activities of major thyme ingredients and lack of (oxidative) DNA damage in V79 Chinese hamster lung fibroblast cells at low levels of carvacrol and thymol. Food and Chemical Toxicology. 47: 2037–2043. doi: 10.1016/j.fct.2009.05.020
  • Gomez, S.A., Abrey-Recalde, M.J., Panek, C.A., Ferrarotti, N.F., Repetto, M.G., Mejías, M.P., Fernández, G.C., Vanzulli, S., Isturiz, M.A., Palermo, M.S. (2013). The Oxidative Stress Induced in Vivo by Shiga Toxin-2 Contributes to The Pathogenicity of Hemolytic Uremic Syndrome. Clinical and Experimental Immunology in press, doi: 10.1111/cei.12124.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.