Skip to main content

Differential regulation of tissue thiol-disulfide redox status in a murine model of peritonitis

Abstract

Background

Glutathione (GSH)/glutathione disulfide (GSSG) and cysteine (Cys)/cystine (CySS) are major redox pools with important roles in cytoprotection. We determined the impact of septic peritonitis on thiol-disulfide redox status in mice.

Methods

FVB/N mice (6–12 week old; 8/group) underwent laparotomy with cecal ligation and puncture (CLP) or laparotomy alone (control). Sections of ileum, colon, lung and liver were obtained and GSH, GSSG, Cys and CySS concentrations determined by HPLC 24 h after laparotomy. Redox potential [Eh in millivolts (mV)] of the GSH/GSSG and Cys/CySS pools was calculated using the Nernst equation. Data were analyzed by ANOVA (mean ± SE).

Results

GSH/GSSG Eh in ileum, colon, and liver was significantly oxidized in septic mice versus control mice (ileum: septic −202±4 versus control −228±2 mV; colon: -195±8 versus −214±1 mV; and liver: -194±3 vs. -210±1 mV, all P<0.01). Lung GSH/GSSG redox was similar in each group (−191±3 versus −190±2 mV). In contrast, ileal and colonic Cys/CySS Eh was unchanged with CLP, while liver and lung Cys/CySS Eh became significantly more reducing (liver: septic = −103±3 versus control −90±2 mV; lung: -101±5 versus −81±1 mV, each P<0.05).

Conclusions

Septic peritonitis induced by CLP oxidizes ileal and colonic GSH/GSSG redox but Cys/CySS Eh remains unchanged in these intestinal tissues. In liver, CLP oxidizes the GSH/GSSG redox pool and CyS/CySS Eh becomes more reducing; in lung, CLP does not alter GSH/GSSG Eh, and Cys/CySS Eh is less oxidized. CLP-induced infection/inflammation differentially regulates major thiol-disulfide redox pools in this murine model.

Background

Sepsis continues to be a primary cause of morbidity and mortality in critically ill patients in intensive care units worldwide[1, 2]. Sepsis, ischemia-reperfusion and inflammatory shock cause oxidative injury to the gut mucosa and depletion of glutathione (GSH)[3, 4]. Glutathione (GSH)/glutathione disulfide (GSSG) and cysteine (Cys)/cystine (CySS) are major redox pools with important roles in cytoprotection, cell function, proliferation, apoptosis, and detoxification[57]. GSH, and its oxidized form GSSG, are the major low-molecular weight thiol antioxidant couple in cells, and play a major role in antioxidant defense and in maintaining cellular thiol-disulfide redox[5, 6]. Intracellular GSH depletion is associated with upregulated levels of pro-inflammatory cytokines[7]. Cysteine (Cys) and its disulfide cystine (CySS) are the most abundant low-molecular weight thiol/disulfide redox couple in plasma[811], but are also present in tissues[8, 11]; an oxidized Cys/CySS redox state increases pro-inflammatory cytokine production during inflammation[9, 11].

Oxidative stress and cytoprotective capacity can be quantitated by determining the redox potentials of Cys/CySS and GSH/GSSG systems[814]. Maintained under stable, but nonequilibrium, steady-state conditions in biological systems, these redox nodes can each be disrupted, to a lesser or greater extent in plasma, tissues, and subcellular fractions depending on the type and severity of oxidative stress[5, 6, 814]. GSH has a central role as a primarily tissue antioxidant; the product of GSH oxidation, GSSG, is reduced back to GSH by GSSG reductase[5, 6]. These redox pools are useful as an index of oxidative stress, as it includes components directly reflecting the availability of GSH for protection against oxidative reactions and the generation of GSSG from oxidative reactions in the correct stoichiometry[12, 13]. Although Cys is regulated independently of GSH during inflammatory and other responses[9, 10, 15], the redox potential or reducing force (Eh) of the GSH/GSSG couple compared to Cys/CySS Eh provides an integrated picture of oxidative stress within a tissue. However, to date there have been no studies exploring concomitant responses of these two redox couples in tissues in response to an oxidative challenge.

Several studies in animal models show that intestinal ischemia, radiation injury, or infection is associated with a decrease in GSH in plasma and tissues and associated organ dysfunction[3, 4, 1619]. Although GSH synthesis is dependent upon the availability of cysteine, little is known regarding regulation of this precursor redox pool in tissue in response to infection. The aim of this study was to determine the concomitant regulation of tissue GSH/GSSG and Cys/CySS redox state in a model of cecal ligation and puncture (CLP)-induced peritonitis in mice.

Methods

Animals and experimental design

Female FVB/N strain mice (6–12 week old) were maintained on a 12 h light–dark schedule in a specific pathogen-free environment with unlimited access to standard laboratory mouse chow. All protocol procedures were approved by the Emory University Institutional Animal Care and Use Committee. A total of 16 study mice were divided into two groups (8/group): 1) mice with CLP-induced peritonitis; and 2) mice without sepsis (sham surgery as control). Mice were subjected to CLP using a 30-gauge needle, an established murine model of septic peritonitis and increased tissue proinflammatory cytokines in our laboratory[20, 21]. This model results in a 27% seven-day mortality rate[20]. Briefly, anesthesia was induced and maintained with isoflurane and 5% oxygen. A small midline abdominal incision was made and the cecum exteriorized and ligated with 4–0 silk immediately distal to the ileocecal valve without causing intestinal obstruction. The cecum was then punctured once with a 30-gauge needle and a small amount of stool was extruded. The cecum was returned to the abdomen and the abdomen wall closed. Mice received 1 mL 0.9% NaCl resuscitation fluid subcutaneously immediately post-operatively and received buprenorphine, 0.1 mg/kg, post-operatively for pain control. Metronidazole (25 mg/kg, Sigma, St. Louis, MO) and ceftriaxone (0.05 mg/kg, Sigma) treatment was initiated 1 hour after CLP and repeated at 12 hours. Animals were sacrificed at 24 hours.

HPLC analyses

Defined segments of full-thickness ileum, colon, lung and liver were derivitized with iodoacetic acid and dansyl chloride. Samples were analyzed by HPLC 24 h after laparotomy and GSH, GSSG, Cys and CySS quantitiated. The Nernst equation was used to calculate the redox potential (Eh, in millivolts or mV) of the GSH/GSSG and Cys/CySS redox pools, respectively, in each tissue. Eh values that are less negative represent a more oxidized redox pool compared to more negative values.

Quantitative real time PCR analysis

Total RNA was extracted using TRIzol (Molecular Research Center, Cincinnati, OH) from proximal ileum and colon. RNA concentration was spectrophotometrically determined at 260nm, and 1ug of total RNA was used to synthesize 10ul of cDNA using the iScript kit (Bio-Rad, Hercules, CA). Quantitative real- time PCR was performed on cDNA samples using iQ SYBR Green Supermix kit (Bio-Rad, Hercules, CA) with the Gene Amp 7000 system (PE Biosystem). Changes in relative gene expression between groups were calculated using the 2-ΔΔCT method with normalization to B-actin. Specific primers were designed using the Primer Express Program (Applied Biosystems, Foster City, CA)[21]. The sequence of primers used were: 5′- AGGCTGCCCCGACTACGT- 3′ (forward) and 5′- GACTTTCTCCTGGTATGAGATAGCAAA-3′ (reverse) for TNF-α, 5′- ACAAGTCGGAGGCTTAATTACACAT-3′ (forward) and 5′- TTGCCATTGCACAACTCTTTTC-3′ (reverse) for IL-6, 5′- ACCCACACTGTGCCCATCTAC-3′ (forward) and 5′- TCGGTGAGGATCTTCATGAGGTA-3′ (reverse) for B-actin.

Statistical analyses

Data were analyzed by unpaired t-test. Results (mean ± SE) were considered significant at p≤ 0.05. Pearson Regression analysis was used to associate cytokine mRNA expression and the GSH/GSSG Eh, the CyS/CySS Eh.

Results

The CLP group exhibited a marked decrease in GSH and a modest increase in GSSG concentration in ileum (Table1), associated with a significantly more oxidized GSH/GSSG Eh versus control mice (Figure1A). In colon, CLP also induced a significant decrease in GSH and an increase in GSSG concentration (Table1) leading to a significantly more oxidized GSH/GSSG Eh (Figure1B). In liver, the CLP group showed a significant 75% decrease in GSH concentrations (Table1). However, in contrast to the CLP response observed in ileum and colon, GSSG levels also fell markedly (50%) in response to CLP-induced peritonitis, suggesting a greater decrease in the hepatic GSH + GSSG pool size. These changes also resulted in a net oxidation of hepatic GSH/GSSG Eh (Figure1C). In lung, CLP induced a modest 25% decrease in GSH concentration but a more marked decrease (50%) in GSSG concentration (Table1). In contrast to the net oxidation of GSH/GSSG pools observed in splanchnic tissues, these changes resulted in no difference in lung GSH/GSSG Eh redox state between CLP-treated and control animals (Figure1D).

Table 1 Tissue GSH and GSSG Concentrations
Figure 1
figure 1

CLP caused a more oxidized GSH/GSSG redox potential in ileum, colon and liver . The Nernst equation was used to calculate the redox potential (Eh, in millivolts or mV) of the GSH/GSSG redox pool in each tissue. Values are mean ± SEM, with an n=8/group. Data shown are from ileum (A), colon (B), liver (C), and lung (D) GSH/GSSG redox potential.* = P< 0.05; **P = < 0.01.

Cys/CySS redox was differentially regulated in these mice compared to GSH/GSSG redox. In ileum, we observed no statistical difference in Cys or CySS concentrations or in Cys/CySS Eh between the CLP and control groups (Table2 and Figure2A). In colon, there was no statistical difference in Cys and CySS concentrations or in Cys/CySS Eh versus control mice (Table2 and Figure2B). In liver, CLP induced a 2.4-fold increase in Cys and a 1.8-fold increase in CySS concentrations, respectively (Table2); however, in direct contrast to the marked oxidation of hepatic GSH/GSSG Eh, the CyS/CySS Eh was modestly but significantly more reducing after CLP administration, probably as a result of increased Cys + CySS pool size (Figure2C). In lung, CLP induced a 2-fold increase in Cys concentrations, while CySS remained unchanged. This resulted in a more reducing Cys/CySS redox status (Figure2D).

Table 2 Tissue Cys and CySS Concentrations
Figure 2
figure 2

CLP caused a more reduced E h Cys/CySS redox potential in liver and lung. The Nernst equation was used to calculate the redox potential (Eh, in millivolts or mV) of the Cys/CySS redox pool in each tissue. Values are mean ± SEM, with an n=8/group. Data shown are from ileum (A), colon (B), liver (C), and lung (D) GSH/GSSG redox potential.* = P< 0.05; **P = < 0.01.

RNA expression levels of pro-inflammatory/anti-inflammatory cytokines were also measured in Ileum, colon, liver and lung. We observed no significant difference in TNF-α and IL-6 expression compared to control between tissues (Table3). There was no significant correlation between cytokine mRNA expression and the GSH/GSSG Eh, the CyS/CySS Eh (not shown).

Table 3 Cytokine mRNA expression in tissue

Discussion

In this study, we show that CLP-induced peritonitis differentially regulates the two major thiol-disulfide redox pools in mouse tissue. Substantial evidence has shown that sepsis and shock is associated with increased oxidative stress and depletion of tissue GSH, which in turn may contribute to organ dysfunction and impaired host response to infection[1719]. Our results show that these redox pools are differentially regulated within and between different organs 24 hr after induction of peritonitis. CLP induced a marked 25%-50% decrease in GSH concentrations in all tissues (ileum, colon, liver and lung). In contrast, GSH disulfide (GSSG) levels increased slightly, but significantly, in ileum and colon, but decreased approximately 50% in liver and lung. These changes resulted in a significant oxidation of the GSH/GSSH Eh in ileum, colon and liver, but no change in redox potential of this pool in lung. Thus, oxidized GSH/GSSG Eh in the intestinal tissues with local peritonitis appears to be due to a combination of decreased GSH and an increase in GSSG concentrations, respectively. In contrast, the oxidation of hepatic GSH/GSSG Eh in this model is likely due to an overall decrease in GSH/GSSG pool size, possibly due to increased requirement for hepatic antioxidant (GSH) defense in response to bacteria and/or bacterial toxins [e.g. lipopolysaccharide (LPS), flagellin] presented to the liver via the portal circulation. Previous studies have shown that CLP induces pro-inflammatory cytokine-mediated lung injury in mice[22]. In addition, CLP-induced peritonitis in rats decreased GSH concentrations in lung in association with markers of lipid peroxidation (oxidative stress) in this tissue[23, 24]. In our study, we also showed a modest, but significant decrease in GSH levels in lung in the CLP group. However, lung appeared to demonstrate an adaptive response to CLP-induced peritoneal infection/inflammation, given the concomitant decrease in GSSG resulting in no change in GSH/GSSG Eh (Figure1D). In our study, we observed no change in TNF-α and IL-6 mRNA expression in lung or other tissues and no correlation with these indices and the GSH/GSSG Eh, the CyS/CySS Eh. Thus, local proinflammatory cytokine expression may not regulate the redox changes were observed, although possible cytokine expression changes at earlier time points after CLP may play a role.

Previous studies by our group have demonstrated that the GSH/GSSG and Cys/CySS redox pools can be differentially regulated under a variety of conditions and essentially reflect distinct redox nodes[15, 25]. In HT-29 human colonic epithelial cells, we found that these thiol/disulfide redox couples were differentially regulated during extracellular oxidation[25]. In mice, we previously showed that administration of LPS oxidized Cys/CySS Eh in lung epithelial lining fluid, although lung tissue was not analyzed[10]. In the current study, we found that CLP-induced peritonitis did not significantly alter Cys or CySS concentrations or Cys/CySS Eh in ileum and colon. In contrast to responses in the two intestinal tissues, CLP resulted in a 2.4-fold upregulation in Cys level and a lesser 1.8-fold increase in CySS levels in liver, resulting in a more reducing Cys/CySS Eh in this tissue. In lung, CLP-induced peritonitis resulted in 2-fold increase in Cys and no change in CySS concentrations, respectively, leading to a modestly more reducing Cys/CySS Eh in this tissue.

The differential regulation of the thiol-disulfide redox pools in ileum, colon and liver examined in our model of infection/inflammation are consistent with in vitro studies of Jones et al.[15], who showed that under conditions of GSH depletion, the Cys/CySS redox couple is not affected, suggesting that the redox state of Cys/CySS is not directly determined by the redox state of GSH/GSSG. A limitation of our study is the lack of systemic plasma redox measures to compare with tissue changes, but in our previous studies in rats, changes in intestinal GSH/GSSG redox pools induced by altering sulfur amino acid intake in diet coincided with similar changes in this pool in plasma[8], while LPS administration in mice oxidized Cys/CySS Eh in lung epithelial lining fluid and in plasma[10]. To our knowledge, this is the first report on concomitant regulation of tissue GSH/GSSG and Cys/CySS redox potentials (Eh) as markers of oxidative stress in a model of infection. In addition, we show that with CLP the lung has homeostatic mechanism(s) to prevent oxidation of the GSH/GSSG redox pool and maintains the Cys/CySS in a more reduced state. There is little information in the literature on the mechanisms that support rapid mobilization of Cys, as suggested by the increase in liver and lung after CLP in our models, but changes in the cellular transporters for CySS and/or Cys or other factors, including protein catabolism could potentially play a role[14]. Our data suggest that the GSH/GSSG redox pool in splanchnic tissue is more sensitive to oxidation in response to local peritonitis that the Cys/CySS pool in this tissue bed. Thus, translational studies on the potential cytoprotective effects of agents to upregulate the GSH pool during peritonitis (e.g. glutamine, n-acetyl-cysteine therapy, dietary sulfur amino acid supplementation) may be of interest[3, 8, 16]. In addition, dietary sulfur amino acid supplementation is a method to increase tissue Cys and thus improve the reducing power of the Cys/CySS redox couple in tissue and to decrease the pro-inflammatory effects of LPS mediated by interleukin-1ß[5, 8, 9, 11, 13]. Because little is known about the functional consequences of altered Cys/CySS redox state in tissue, further work is needed to understand both the regulation and role of this redox couple, including as it relates to changes in tissue GSH/GSSG Eh, in models of infection/inflammation.

Conclusions

Septic peritonitis induced by CLP oxidizes ileal and colonic GSH/GSSG redox but Cys/CySS Eh remains unchanged. In liver, CLP oxidizes the GSH/GSSG redox pool and CyS/CySS Eh becomes more reducing; in lung, CLP does not alter GSH/GSSG Eh, and Cys/CySS Eh is less oxidized. CLP-induced infection/inflammation differentially regulates major thiol-disulfide redox pools in this murine model.

Abbreviations

GSH:

Glutathione

GSSG:

Glutathione Disulfide

Cys:

Cysteine

CySS:

Cystine

CLP:

Cecal Ligation and Puncture

HPLC:

High Performance Liquid Chromatography

LPS:

Lipopolysaccharide.

References

  1. Martin GS, Mannino DM, Moss M: The effect of age on the development and outcome of adult sepsis. Crit Care Med. 2006, 34: 15-21. 10.1097/01.CCM.0000194535.82812.BA.

    Article  PubMed  Google Scholar 

  2. Klevens RM, Morrison MA, Nadle J, Petit S, Gershman K, Ray S, Harrison LH, Lynfield R, Dumyati G, Townes JM, Craig AS, Zell ER, Fosheim GE, McDougal LK, Carey RB, Fridkin SK: Invasive methicillin-resistant Staphylococcus aureus infections in the United States. JAMA. 2007, 298 (15): 1763-1771. 10.1001/jama.298.15.1763.

    Article  CAS  PubMed  Google Scholar 

  3. Harward TR, Coe D, Souba WW, Klingman N, Seeger JM: Glutamine preserves gut glutathione levels during intestinal ischemia/reperfusion. J Surg Res. 1994, 20 (56): 351-535.

    Article  Google Scholar 

  4. Macdonald J, Galley HF, Webster NR: Oxidative stress and gene expression in sepsis. Br J Anaesth. 2003, 90: 221-232. 10.1093/bja/aeg034.

    Article  CAS  PubMed  Google Scholar 

  5. Go YM, Jones DP: Redox compartmentalization in eukaryotic cells. Biochim Biophys Acta. 2008, 1780: 1273-1290. 10.1016/j.bbagen.2008.01.011.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  6. Jones DP: Radical-free biology of oxidative stress. Am J Physiol. 2008, 295: C849-C868. 10.1152/ajpcell.00283.2008.

    Article  CAS  Google Scholar 

  7. Haddad JJ: A redox microenvironment is essential for MAPK-dependent secretion of pro-inflammatory cytokines: modulation by glutathione (GSH/GSSG) biosynthesis and equilibrium in the alveolar epithelium. Cell Immunol. 2011, 270: 53-61. 10.1016/j.cellimm.2011.04.001.

    Article  CAS  PubMed  Google Scholar 

  8. Nkabyo Y, Gu LH, Jones DP, Ziegler TR: Thiol/disulfide redox status is oxidized in plasma and small intestinal and colonic mucosa of rats with inadequate sulfur amino acid intake. J Nutr. 2006, 136: 1242-1248.

    CAS  PubMed  Google Scholar 

  9. Iyer SS, Accardi CJ, Ziegler TR, Blanco RA, Ritzenthaler JD, Rojas M, Roman J, Jones DP: Cysteine Redox Potential Determines Pro-Inflammatory IL-1ß Levels. PLoS One. 2009, 4: e5017-10.1371/journal.pone.0005017.

    Article  PubMed Central  PubMed  Google Scholar 

  10. Iyer SS, Jones DP, Brigham KL, Rojas M: Oxidation of Plasma Cysteine/Cystine Redox State in Endotoxin-Induced Lung Injury. Am J Respir Cell Mol Biol. 2009, 40: 90-98.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  11. Go YM, Jones DP: Cysteine/cystine redox signaling in cardiovascular disease. Free Radic Biol Med. 2011, 50: 495-509. 10.1016/j.freeradbiomed.2010.11.029.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Jones DP, Liang Y: Measuring the poise of thiol/disulfide couples in vivo. Free Radic Biol Med. 2009, 47: 1329-1338. 10.1016/j.freeradbiomed.2009.08.021.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  13. Go YM, Jones DP: Redox clamp model for study of extracellular thiols and disulfides in redox signaling. Methods Enzymol. 2010, 474: 165-179.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  14. Mannery YO, Ziegler TR, Hao L, Shyntum Y, Jones DP: Characterization of apical and basal thiol-disulfide redox regulation in human colonic epithelial cells. Am J Physiol Gastrointest Liver Physiol. 2010, 299: G523-G530. 10.1152/ajpgi.00359.2009.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  15. Jones DP, Go YM, Anderson CL, Ziegler TR, Kinkade JM, Kirlin WG: Cysteine/cystine couple is a newly recognized node in the circuitry for biologic redox signaling and control. FASEB J. 2004, 18: 1246-1248.

    CAS  PubMed  Google Scholar 

  16. Neal R, Matthews RH, Lutz P, Ercal N: Antioxidant role of N-acetyl cysteine isomers following high dose irradiation. Free Radic Biol Med. 2003, 34: 689-695. 10.1016/S0891-5849(02)01372-2.

    Article  CAS  PubMed  Google Scholar 

  17. Villa P, Saccani A, Sica A, Ghezzi P: Glutathione protects mice from lethal sepsis by limiting inflammation and potentiating host defense. J Infect Dis. 2002, 185: 1115-1120. 10.1086/340042.

    Article  CAS  PubMed  Google Scholar 

  18. Ko K, Yang H, Noureddin M, Iglesia-Ara A, Xia M, Wagner C, Luka Z, Mato JM, Lu SC: Changes in S-adenosylmethionine and GSH homeostasis during endotoxemia in mice. Lab Invest. 2008, 88: 1121-1129. 10.1038/labinvest.2008.69.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  19. Robinson MK, Rounds JD, Hong RW, Jacobs DO, Wilmore DW: Glutathione deficiency increases organ dysfunction after hemorrhagic shock. Surgery. 1992, 112: 140-147.

    CAS  PubMed  Google Scholar 

  20. Turnbull IR, Clark AT, Stromberg PE, Dixon DJ, Woolsey CA, Davis CG, Hotchkiss RS, Buchman TG, Coopersmith CM: Effects of aging on the immunopathologic response to sepsis. Crit Care Med. 2009, 37: 1018-1023. 10.1097/CCM.0b013e3181968f3a.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  21. Clark JA, Gan H, Samocha AJ, Fox AC, Buchman TG, Coopersmith CM: Enterocyte-specific epidermal growth factor prevents barrier dysfunction and improves mortality in murine peritonitis. Am J Physiol Gastrointest Liver Physiol. 2009, 297: G471-G479. 10.1152/ajpgi.00012.2009.

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  22. Bodas M, Min T, Vij N: Early-age-related changes in proteostasis augment immunopathogenesis of sepsis and acute lung injury. PLoS One. 2010, 5: e15480-10.1371/journal.pone.0015480.

    Article  PubMed Central  PubMed  Google Scholar 

  23. Koksal GM, Sayilgan C, Aydin S, Oz H, Uzun H: Correlation of plasma and tissue oxidative stresses in intra-abdominal sepsis. J Surg Res. 2004, 122: 180-183. 10.1016/j.jss.2004.07.246.

    Article  CAS  PubMed  Google Scholar 

  24. Coskun AK, Yigiter M, Oral A, Odabasoglu F, Halici Z, Mentes O, Cadirci E, Atalay F, Suleyman H: The effects of montelukast on antioxidant enzymes and proinflammatory cytokines on the heart, liver, lungs, and kidneys in a rat model of cecal ligation and puncture-induced sepsis. Sci World J. 2011, 11: 1341-1356.

    Article  CAS  Google Scholar 

  25. Anderson CL, Iyer SS, Ziegler TR, Jones DP: Control of extracellular cysteine/cystine redox state by HT-29 cells is independent of cellular glutathione. Am J Physiol Regul Integr Comp Physiol. 2007, 293: R1069-R1075. 10.1152/ajpregu.00195.2007.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported by National Institutes of Health grant K24 RR023356 (TRZ), T32 DK 007734 (SMB), ES009047 (DPJ), ES011195 (DPJ) and R01 GM072808 (CMC).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Shana M Benton.

Additional information

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

TRZ and CMC conceived the study, SMB, ZL, and LH collected the samples; ZL performed the CLP surgeries and maintained the mice; DPJ and YL performed redox analysis; SMB and DPJ analyzed the data; SMB and TRZ authored the manuscript; SMB, GH, TRZ, DPJ, and CMC prepared the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Benton, S.M., Liang, Z., Hao, L. et al. Differential regulation of tissue thiol-disulfide redox status in a murine model of peritonitis. J Inflamm 9, 36 (2012). https://doi.org/10.1186/1476-9255-9-36

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1476-9255-9-36

Keywords