Considering the Effect of Rosa damascena Mill. Essential Oil on Oxidative Stress and COX-2 Gene Expression in the Liver of Septic Rats
Journal: 2020/May - Turkish Journal of Pharmaceutical Sciences
Abstract:
Objectives: Sepsis is a clinical illness with a high rate of mortality all over the world. Oxidative stress is considered the main phenomenon that occurs in sepsis. Rosa damascena Mill. is an ancient herbal plant with high pharmacological activities.
Materials and methods: Cecal ligation and puncture (CLP) as a standard model was used to induce sepsis in rats. Male adult rats were randomly divided into 5 groups. Different doses of R. damascena essential oil (50 and 100 mg/kg.bw) were gavaged orally for 14 days and on day 15 CLP was performed. After 24 h, blood samples and liver tissues were removed in order to measure oxidative stress [myeloperoxidase (MPO), malondialdehyde (MDA), glutathione (GSH), glutathione-S-transferase, and ferric reducing ability of plasma (FRAP)] and biochemical parameters [alkaline phosphatase (ALP), aspartate transaminase (AST), alanine transaminase (ALT), and bilirubin] together with plasma prostaglandin E2 (PGE2) and COX-2 expression.
Results: The essential oil was capable of modulating all of the oxidative stress, antioxidant, and anti-inflammatory parameters induced by CLP as characterized by elevations in MPO and MDA levels as well as increases in AST and ALT concentrations concomitant with PGE2 and COX-2 increments. The antioxidant defense system such as GSH and FRAP was also increased in the essential oil treated groups.
Conclusion: Our results showed that the essential oil has antioxidative and hepatoprotective activities through reducing the oxidative injury in sepsis caused by CLP.
Keywords: CLP; Rosa damascena Mill.; Sepsis; hepatoprotective activity; oxidative stress.
Relations:
Content
Conditions
(1)
Drugs
(4)
Chemicals
(9)
Processes
(2)
Anatomy
(1)
Similar articles
Articles by the same authors
Discussion board
Turk J Pharm Sci 16(4): 416-424

Considering the Effect of <em>Rosa damascena</em> Mill. Essential Oil on Oxidative Stress and <em>COX-2</em> Gene Expression in the Liver of Septic Rats

Islamic Azad University, Qom Branch, Faculty of Medicine, Department of Medicine, Qom, Iran
Nuclear Science and Technology Research Institute, Materials and Nuclear Fuel Research School, Tehran, Iran
Islamic Azad University, Garmsar Branch, Faculty of Veterinary Medicine, Department of Pathobiology, Garmsar, Iran
Hakim Sabzevari University, Faculty of Science, Department of Biology, Sabzevar, Iran
Payame-e-Noor University, Faculty of Sciences, Department of Biochemistry, Tehran, Iran
* Address for Correspondence: Phone: +989122490620 E-mail:moc.oohay@oib_hahkdad
Received 2018 Apr 29; Accepted 2018 Jul 31.

Abstract

Objectives:

Sepsis is a clinical illness with a high rate of mortality all over the world. Oxidative stress is considered the main phenomenon that occurs in sepsis. Rosa damascena Mill. is an ancient herbal plant with high pharmacological activities.

Materials and Methods:

Cecal ligation and puncture (CLP) as a standard model was used to induce sepsis in rats. Male adult rats were randomly divided into 5 groups. Different doses of R. damascena essential oil (50 and 100 mg/kg.bw) were gavaged orally for 14 days and on day 15 CLP was performed. After 24 h, blood samples and liver tissues were removed in order to measure oxidative stress [myeloperoxidase (MPO), malondialdehyde (MDA), glutathione (GSH), glutathione-S-transferase, and ferric reducing ability of plasma (FRAP)] and biochemical parameters [alkaline phosphatase (ALP), aspartate transaminase (AST), alanine transaminase (ALT), and bilirubin] together with plasma prostaglandin E2 (PGE2) and COX-2 expression.

Results:

The essential oil was capable of modulating all of the oxidative stress, antioxidant, and anti-inflammatory parameters induced by CLP as characterized by elevations in MPO and MDA levels as well as increases in AST and ALT concentrations concomitant with PGE2 and COX-2 increments. The antioxidant defense system such as GSH and FRAP was also increased in the essential oil treated groups.

Conclusion:

Our results showed that the essential oil has antioxidative and hepatoprotective activities through reducing the oxidative injury in sepsis caused by CLP.

Keywords: Sepsis, Rosa damascena Mill., oxidative stress, CLP, hepatoprotective activity

Objectives:

Sepsis is a clinical illness with a high rate of mortality all over the world. Oxidative stress is considered the main phenomenon that occurs in sepsis. Rosa damascena Mill. is an ancient herbal plant with high pharmacological activities.

Materials and Methods:

Cecal ligation and puncture (CLP) as a standard model was used to induce sepsis in rats. Male adult rats were randomly divided into 5 groups. Different doses of R. damascena essential oil (50 and 100 mg/kg.bw) were gavaged orally for 14 days and on day 15 CLP was performed. After 24 h, blood samples and liver tissues were removed in order to measure oxidative stress [myeloperoxidase (MPO), malondialdehyde (MDA), glutathione (GSH), glutathione-S-transferase, and ferric reducing ability of plasma (FRAP)] and biochemical parameters [alkaline phosphatase (ALP), aspartate transaminase (AST), alanine transaminase (ALT), and bilirubin] together with plasma prostaglandin E2 (PGE2) and COX-2 expression.

Results:

The essential oil was capable of modulating all of the oxidative stress, antioxidant, and anti-inflammatory parameters induced by CLP as characterized by elevations in MPO and MDA levels as well as increases in AST and ALT concentrations concomitant with PGE2 and COX-2 increments. The antioxidant defense system such as GSH and FRAP was also increased in the essential oil treated groups.

Conclusion:

Our results showed that the essential oil has antioxidative and hepatoprotective activities through reducing the oxidative injury in sepsis caused by CLP.

Acknowledgments

This research was conducted by the Research Deputy Grand of Qom Branch, Islam Azad University.

Footnotes

Conflict of Interest: No conflict of interest was declared by the authors.

References

  • 1. Angus DC, van der Poll TSevere sepsis and septic shock. N Engl J Med. 2013;369:840–851.[PubMed][Google Scholar]
  • 2. Peters K, Unger RE, Brunner J, Kirkpatrick CJMolecular basis of endothelial dysfunction in sepsis. Cardiovasc Res. 2003;60:49–57.[PubMed][Google Scholar]
  • 3. Peters J, Cohen JSepsis. Med J. 2013;41:667–669.[PubMed][Google Scholar]
  • 4. Cho SY, Choi JHBiomarkers of sepsis. Infect Chemother. 2014;46:1–12.[Google Scholar]
  • 5. Nelson GE, Mave V, Gupta ABiomarkers for sepsis: A review with special attention to India. Biomed Res Int. 2014;2014:264351.[Google Scholar]
  • 6. Li S, Zhu FX, Zhao XJ, An YZThe immunoprotective activity of interleukin-33 in a mouse model of cecal ligation and puncture-induced sepsis. Immunol Lett. 2016;169:1–7.[PubMed][Google Scholar]
  • 7. Koh HJ, Joo J, Cho ML, Her YM, Hwang JE, Lee JProinflammatory and anti-inflammatory cytokine balance in patients with cirrhotic hepatitis during live-donor liver transplant. Exp Clin Transplant. 2013;11:39–43.[PubMed][Google Scholar]
  • 8. Lowes DA, Webster NR, Murphy MP, Galley HFAntioxidants that protect mitochondria reduce interleukin-6 and oxidative stress, improve mitochondrial function, and reduce biochemical markers of organ dysfunction in a rat model of acute sepsis. Br J Anaesth. 2013;110:472–480.[Google Scholar]
  • 9. Dejager L, Pinheiro I, Dejonckheere E, Libert CCecal ligation and puncture: the gold standard model for polymicrobial sepsis? Trends Microbiol. 2011;19:198–208.[PubMed][Google Scholar]
  • 10. Song T, Yin H, Chen J, Huang L, Jiang J, He T, Huang H, Hu XSurvival advantage depends on cecal volume rather than cecal length in a mouse model of cecal ligation and puncture. J Surg Res. 2016;203:476–482.[PubMed][Google Scholar]
  • 11. Schabbauer GPolymicrobial sepsis models: CLP versus CASP. Drug Discov Today Dis Models. 2012;9:17–21.[PubMed][Google Scholar]
  • 12. Cuenca AG, Delano MJ, Kelly-Scumpia KM, Moldawer LL, Efron PACecal ligation and puncture. Curr Protoc Immunol. 2010;91:19.13.1–19.13.11.[PubMed][Google Scholar]
  • 13. Hajhashemi V, Ghannadi A, Hajiloo MAnalgesic and anti-inflammatory effects of Rosa damascena hydroalcoholic extract and its essential oil in animal models. Iran J Pharm Res. 2010;9:163–168.[Google Scholar]
  • 14. Mahboubi MRosa damascena as holy ancient herb with novel applications. J Tradit Complement Med. 2015;6:10–16.[Google Scholar]
  • 15. Dolati K, Rakhshandeh H, Shafei MNAntidepressant-like effect of aqueous extract from Rosa damascena in mice. Avicenna J Phytomed. 2011;1:91–97.[PubMed][Google Scholar]
  • 16. Akbari M, Kazerani HR, Kamrani A, Mohri MA preliminary study on some potential toxic effects of Rosa damascena Mill. Iran J Vet Res. 2013;14:232–236.[PubMed][Google Scholar]
  • 17. Gholamhoseinian A, Fallah H, Sharifi far F. Inhibitory effect of methanol extract of Rosa damascena Mill. flowers on α-glucosidase activity and postprandial hyperglycemia in normal and diabetic rats. Phytomedicine. 2009;16:935–941.[PubMed]
  • 18. Achuthan CR, Babu BH, Padikkala JAntioxidant and hepatoprotective effects of Rosa damascena. Pharm Biol. 2003;41:357–361.[PubMed][Google Scholar]
  • 19. Baydar NG, Baydar HPhenolic compounds, antiradical activity and antioxidant capacity of oil-bearing rose (Rosa damascena Mill.) extracts. Ind Crops Prod. 2013;41:375–380.[PubMed][Google Scholar]
  • 20. Yassa N, Masoomi F, Rohani Rankouhi SE, Hadjiakhoondi AChemical composition and antioxidant activity of the extract and essential oil of Rosa damascena from Iran, population of Guilan. DARU J Pharm Sci. 2009;17:175–180.[PubMed][Google Scholar]
  • 21. Sedlak J, Lindsay RHEstimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem. 1968;25:192–205.[PubMed][Google Scholar]
  • 22. Hillegass LM, Griswold DE, Brickson B, Albrightson-Winslow CAssessment of myeloperoxidase activity in whole rat kidney. J Pharmacol Methods. 1990;24:285–295.[PubMed][Google Scholar]
  • 23. Buege JA, Aust SDMicrosomal lipid peroxidation. Methods Enzymol. 1978;52:302–310.[PubMed][Google Scholar]
  • 24. Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases. The first enzymatic step in mercapturic acid formation. J Biol Chem. 1974;249:7130–7139.[PubMed]
  • 25. Benzie IF, Strain JJThe ferric reducing ability of plasma (FRAP) as a measure of “antioxidant power”: the FRAP assay. Anal Biochem. 1996;239:70–76.[PubMed][Google Scholar]
  • 26. Zolali E, Hamishehkar H, Maleki-Dizaji N, Majidi Zolbanin N, Ghavimi H, Kouhsoltani M, Asgharian PSelenium effect on oxidative stress factors in septic rats. Adv Pharm Bull. 2014;4:289–293.[Google Scholar]
  • 27. Abd El Tawab AM, Shahin NN, AbdelMohsen MMProtective effect of Satureja montana extract on cyclophosphamide-induced testicular injury in rats. Chem Biol Interact. 2014;224:196–205.[PubMed][Google Scholar]
  • 28. Makled MN, El-Awady MS, Abdelaziz RR, Atwan N, Guns ET, Gameil NM, Shehab El-Din AB, Ammar EMPomegranate protects liver against cecal ligation and puncture-induced oxidative stress and inflammation in rats through TLR4/NF-B pathway inhibition. Environ Toxicol Pharmacol. 2016;43:182–192.[PubMed][Google Scholar]
  • 29. Cuzzocrea S, Mazzon E, Dugo L, Serraino I, Ciccolo A, Centorrino T, De Sarro A, Caputi APProtective effects of n-acetylcysteine on lung injury and red blood cell modification induced by carrageenan in the rat. FASEB J. 2001;15:1187–1200.[PubMed][Google Scholar]
  • 30. Mohamadin AM, Elberry AA, Abdel Gawad HS, Morsy GM, Al-Abbasi FAProtective effects of simvastatin, a lipid-lowering agent, against oxidative damage in experimental diabetic rats. J Lipids. 2011;2011:167958.[Google Scholar]
  • 31. Sener G, Arbak S, Kurtaran P, Gedik N, Yeğen BCEstrogen protects the liver and intestines against sepsis-induced injury in rats. J Surg Res. 2005;128:70–78.[PubMed][Google Scholar]
  • 32. Ozdulger A, Cinel I, Koksel O, Cinel L, Avlan D, Unlu A, Okcu H, Dikmengil M, Oral UThe protective effect of N-acetylcysteine on apoptotic lung injury in cecal ligation and puncture-induced sepsis model. Shock. 2003;19:366–372.[PubMed][Google Scholar]
  • 33. Zhong W, Qian K, Xiong J, Ma K, Wang A, Zou YCurcumin alleviates lipopolysaccharide-induced sepsis and liver failure by suppression of oxidative stress-related inflammation via PI3K/AKT and NF-kB related signaling. Biomed Pharmacother. 2016;83:302–313.[PubMed][Google Scholar]
  • 34. Bouzenna H, Dhibi S, Samout N, Rjeibi I, Talarmin H, Elfeki A, Hfaiedh NThe protective effect of Citrus limon essential oil on hepatotoxicity and nephrotoxicity induced by aspirin in rats. Biomed Pharmacother. 2016;83:1327–1334.[PubMed][Google Scholar]
  • 35. Dadkhah A, Fatemi F, Kazemnejad S, Rasmi Y, Ashrafi-Helan J, Allameh ADifferential effects of acetaminophen on enzymatic and non-enzymatic antioxidant factors and plasma total antioxidant capacity in developing and adult rats. Mol Cell Biochem. 2006;281:145–152.[PubMed][Google Scholar]
  • 36. Frencken JF, van Vught LA, Peelen LM, Ong DSY, Klein Klouwenberg PMC, Horn J, Bonten MJM, van der Poll T, Cremer OL; MARS ConsortiumAn unbalanced inflammatory cytokine response is not associated with mortality following sepsis: A prospective cohort study. Crit Care Med. 2017;45:e493–e499.[PubMed][Google Scholar]
  • 37. Huang YH, Tsai PS, Huang CJBupivacaine inhibits COX-2 expression, PGE2, and cytokine production in endotoxin-activated macrophages. Acta Anaesthesiol Scand. 2008;52:530–535.[PubMed][Google Scholar]
  • 38. Li B, Li YM, Li X, Shi B, He MY, Zhu XL, Zhou WC, Wachtel MS, Frezza ECOX-2 inhibition improves immune system homeostasis and decreases liver damage in septic rats. J Surg Res. 2009;157:43–47.[PubMed][Google Scholar]
  • 39. Hussein RRS, Soliman RH, Abdelhaleem Ali AM, Tawfeik MH, Abdelrahim MEAEffect of antiepileptic drugs on liver enzymes. Beni-Seuf Univ J Appl Sci. 2013;2:14–19.[PubMed][Google Scholar]
Collaboration tool especially designed for Life Science professionals.Drag-and-drop any entity to your messages.