The DOI matches its Crossref record; 310 of the 310 references it cites were found in a registry or an index.
Inducible Nitric Oxide Synthase and Inflammatory Diseases
Open accessAbstract
Nitric oxide (NO) is a colorless gas at room temperature and one of the simplest molecules known, yet it has been implicated in a wide variety of regulatory mechanisms ranging from vasodilatation and blood pressure control to neurotransmission. It is also involved in nonspecific immunity and participates in the complex mechanism of tissue injury as a major mediator of inflammatory processes and apoptosis ( 1 ). This work focuses on the complex role of NO produced by the inducible form of nitric oxide synthase (iNOS) in inflammatory and autoimmune diseases. Although the earliest studies in the field suggested that NO is a strictly pro-inflammatory macrophage product, it is clear from the current literature that, in fact, NO is made by numerous cell types and is often anti-inflammatory. Much of this dichotomy can be explained by the particular responses of given cells involved in the inflammatory response, but another variable involves the complex chemistry in which NO can participate. As we outline below, various facets of the immune response can be examined from these perspectives.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Atherosclerosis--an inflammatory disease
Ross, R. (1999) · New England Journal of Medicine · doi:10.1056/nejm199901143400207 · Cited by 21,725
Nitric oxide: physiology, pathophysiology, and pharmacology.
Moncada, S., Palmer, R. M., & Higgs, E. A. (1991) · Pharmacological Reviews · doi:10.1016/s0031-6997(25)06663-3 · Cited by 15,525
Nitric oxide, superoxide, and peroxynitrite: the good, the bad, and ugly
Beckman, J. S., & Koppenol, W. H. (1996) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1996.271.5.c1424 · Cited by 5,513
Functional diversity of helper T lymphocytes
Abbas, A. K., Murphy, K. M., & Sher, A. (1996) · Nature · doi:10.1038/383787a0 · Cited by 4,450
NITRIC OXIDE AND MACROPHAGE FUNCTION
MacMicking, J., Xie, Q.-W., & Nathan, C. (1997) · Annual Review of Immunology · doi:10.1146/annurev.immunol.15.1.323 · Cited by 4,211
The expanding universe of T-cell subsets: Th1, Th2 and more
Mosmann, T. R., & Sad, S. (1996) · Immunology Today · doi:10.1016/0167-5699(96)80606-2 · Cited by 3,633
Nitric oxide: an endogenous modulator of leukocyte adhesion.
Kubes, P., Suzuki, M., & Granger, D. N. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.11.4651 · Cited by 3,029
Nitric oxide synthases: Roles, tolls, and controls
Nathan, C., & Xie, Q.-W. (1994) · Cell · doi:10.1016/0092-8674(94)90266-6 · Cited by 2,918
Secretory products of macrophages.
Nathan, C. F. (1987) · Journal of Clinical Investigation · doi:10.1172/jci112815 · Cited by 2,615
Endothelial cells in physiology and in the pathophysiology of vascular disorders.
Cines, D. B., Pollak, E. S., Buck, C. A., Loscalzo, J., Zimmerman, G. A., McEver, R. P., Pober, J. S., Wick, T. M., Konkle, B. A., Schwartz, B. S., et al. (1998) · PubMed · doi:10.1182/blood.v91.10.3527 · Cited by 2,256
Research works printed but not linked: 55
- Groeneveld PH, Kwappenberg KM, Langermans JA, et al. (1997) Relation between pro- and anti-inflammatory cytokines and the production of nitric oxide (NO) in severe sepsis. Cytokine. 9: 138–142. · doi:10.1006/cyto.1996.0147
- Pender BS, Chen H, Ashton S, et al. (1996) Transforming growth factor β 1 alters rat peritoneal macrophage mediator production and improves survival during endotoxic shock. Eur. Cytokine Netw. 7: 137–142.
- Salvemini D, Seibert K, Marino MH. (1996) PG release, as a consequence of NO-driven COX activation, contributes to the proinflammatory effects of NO. Drugs News Perspect. 4: 204–219.
- Bulut V, Severn A, Liew FY. (1993) Nitric oxide production by murine macrophages is inhibited by prolonged elevation of cyclic AMP. Biochem. Biophys. Res. Commun. 195: 1134–1138. · doi:10.1006/bbrc.1993.2162
- Kepka-Lenhart D, Chen L-C, Morris SM. (1996) Novel actions of aspirin and sodium salicylate: discordant effects on nitric oxide synthesis and induction of nitric oxide synthase mRNA in a murine macrophage cell line. J. Leukoc. Biol. 59: 840–846. · doi:10.1002/jlb.59.6.840
- Harbrecht BG, Kim YM, Wirant EA, et al. (1997) Timing of prostaglandin exposure is critical for the inhibition of LPS- or IFN-γ-induced macrophage NO synthesis by PGE2. J. Leukoc. Biol. 61: 712–720. · doi:10.1002/jlb.61.6.712
- Cuzzocrea S, Costantino G, Zingarelli B, et al. (1999) Protective effects of poly (ADP-ribose) synthase inhibitors in zymosan-activated plasma induced paw edema. Life Sci. 65: 957–964. · doi:10.1016/s0024-3205(99)00325-2
- Wong HR, Finder JD, Wasserloos K, et al. (1996) Transcriptional regulation of iNOS by IL-1 β in cultured rat pulmonary artery smooth muscle cells. Am. J. Physiol. 271: L166–L171.
- Shoker AS, Yang H, Murabit MA, et al. (1997) Analysis of the in vitro effect of exogenous nitric oxide on human lymphocytes. Mol. Cell Biochem. 171: 75–83. · doi:10.1023/a:1006815430622
- Taylor-Robinson AW. (1997) Counter-regulation of T helper 1 cell proliferation by nitric oxide and interleukin-2. Biochem. Biophys. Res. Commun. 233: 14–19. · doi:10.1006/bbrc.1997.6386
- Kosonen O, Kankaanranta H, Lahde M, et al. (1998) Nitric oxide-releasing oxatriazole derivatives inhibit human lymphocyte proliferation by a cyclic GMP-independent mechanism. J. Pharmacol. Exp. Ther. 286: 215–220. · doi:10.1016/s0022-3565(24)37577-9
- Gabbai FB, Boggiano C, Peter T, et al. (1997) Inhibition of inducible nitric oxide synthase intensifies injury and functional deterioration in autoimmune interstitial nephritis. J. Immunol. 159: 6266–6275. · doi:10.4049/jimmunol.159.12.6266
- Hoffman RA, Langrehr JM, Berry LM, et al. (1996) Bystander injury of host lymphoid tissue during murine graft-versus-host disease is mediated by nitric oxide. Transplantation 61: 610–618. · doi:10.1097/00007890-199602270-00016
- Falzarano G, Krenger W, Snyder KM, et al. (1996) Suppression of B-cell proliferation to lipopolysaccharide is mediated through induction of the nitric oxide pathway by tumor necrosis factor-α in mice with acute graft-versus-host disease. Blood 87: 2853–2860. · doi:10.1182/blood.v87.7.2853.bloodjournal8772853
- Winlaw DS, Schyvens CG, Smythe GA, et al. (1995) Selective inhibition of nitric oxide production during cardiac allograft rejection causes a small increase in graft survival. Transplantation 60: 77–82. · doi:10.1097/00007890-199507150-00015
- Tanaka S, Kamiike W, Ito T, et al. (1995) Generation of nitric oxide as a rejection marker in rat pancreas transplantation. Transplantation 60: 713–717. · doi:10.1097/00007890-199510150-00017
- Santos LL, Morand EF, Yang Y, et al. (1997) Suppression of adjuvant arthritis and synovial macrophage inducible nitric oxide by N-iminoethyl-l-ornithine, a nitric oxide synthase inhibitor. Inflammation 21: 299–311. · doi:10.1023/a:1027397816209
- Miesel R, Kurpisz M, Kroger H. (1996) Suppression of inflammatory arthritis by simultaneous inhibition of nitric oxide synthase and NADPH oxidase. Free Radic. Biol. Med. 20: 75–81. · doi:10.1016/0891-5849(95)02026-8
- Gassner R, Buckley MJ, Georgescu H, et al. (1999) Cyclic tensile stress exerts antiinflammatory actions on chondrocytes by inhibiting inducible nitric oxide synthase. J. Immunol. 163: 2187–2192. · doi:10.4049/jimmunol.163.4.2187
- Borderie D, Hilliquin P, Hernvann A, et al. (1999) Apoptosis induced by nitric oxide is associated with nuclear p53 protein expression in cultured osteoarthritic synoviocytes. Osteoarthritis. Cartilage. 7: 203–213. · doi:10.1053/joca.1998.0209
- Rothe H, Kolb H. (1999) Strategies of protection from nitric oxide toxicity in islet inflammation. J. Mol. Med. 77: 40–44. · doi:10.1007/s001090050298
- Whittle BJ. (1997) Nitric oxide-a mediator of inflammation or mucosal defence. Eur. J. Gastroenterol. Hepatol. 9: 1026–1032. · doi:10.1097/00042737-199711000-00002
- Mourelle M, Vilaseca J, Guarner F, et al. (1996) Toxic dilatation of colon in a rat model of colitis is linked to an inducible form of nitric oxide synthase. Am. J. Physiol. 270: G425–G430.
- Dimmeler S, Haendeler J, Nehls M, et al. (1997) Suppression of apoptosis by nitric oxide via inhibition of interleukin-1β-converting enzyme (ICE)-like and cysteine protease protein (CPP)-32-like proteases. J. Exp. Med. 185: 601–607. · DOI · Paper page
- Scott L, Kerr A, Haydock D, et al. (1997) Subendothelial proteoglycan synthesis and transforming growth factor β distribution correlate with susceptibility to atherosclerosis. J. Vasc. Res. 34: 365–377. · doi:10.1159/000159245
- Tsuji M, Dimov VB, Yoshida T. (1995) In vivo expression of monokine and inducible nitric oxide synthase in experimentally induced pulmonary granulomatous inflammation. Evidence for sequential production of interleukin-1, inducible nitric oxide synthase, and tumor necrosis factor. Am. J. Pathol. 147: 1001–1015.
- Nozaki Y, Hasegawa Y, Takeuchi A, et al. (1997) Nitric oxide as an inflammatory mediator of radiation pneumonitis in rats. Am. J. Physiol. 272: L651–L658.
- Moncada S. (1994) Nitric oxide. J. Hypertens. Suppl. 12: S35–S39.
- Ruschitzka F, Corti R, Noll G, et al. (1999) A rationale for treatment of endothelial dysfunction in hypertension. J. Hypertens. Suppl 17: S25–S35.
- Wigand R, Meyer J, Busse R, et al. (1997) Increased serum NG-hydroxy-l-arginine in patients with rheumatoid arthritis and systemic lupus erythematosus as an index of an increased nitric oxide synthase activity. Ann. Rheum. Dis. 56: 330–332. · doi:10.1136/ard.56.5.330
- Harper L, Savage CO. (1999) Mechanisms of endothelial injury in systemic vasculitis. Adv. Nephrol. Necker Hosp. 29: 1–15.
- Borderie D, Hilliquin P, Hernvann A, et al. (1999) Nitric oxide synthase is expressed in the lymphomononuclear cells of synovial fluid in patients with rheumatoid arthritis. J. Rheumatol. 26: 2083–2088.
- Salvatierra J, Escames G, Hernandez P, et al. (1999) Cartilage and serum levels of nitric oxide in patients with hip osteoarthritis. J. Rheumatol. 26: 2015–2017.
- Kwon OJ, Kim JH, Kim HC, et al. (1998) Nitric oxide expression in airway epithelial cells in response to tubercle bacilli stimulation. Respirology. 3: 119–124. · doi:10.1111/j.1440-1843.1998.tb00109.x
- Rogers DF, Laurent GJ. (1998) New ideas on the pathophysiology and treatment of lung disease. Thorax 53: 200–203. · doi:10.1136/thx.53.3.200
- Zamora SA, Amin HJ, McMillan DD, et al. (1997) Plasma l-arginine concentrations in premature infants with necrotizing enterocolitis. J. Pediatr. 131: 226–232. · doi:10.1016/s0022-3476(97)70158-6
- Sigge W, Wedel T, Kuhnel W, et al. (1998) Morphologic alterations of the enteric nervous system and deficiency of non-adrenergic non-cholinergic inhibitory innervation in neonatal necrotizing enterocolitis. Eur. J. Pediatr. Surg. 8: 87–94. · doi:10.1055/s-2008-1071128
- Beckett CG, Dell’Olio D, Ellis HJ, et al. (1998) The detection and localization of inducible nitric oxide synthase production in the small intestine of patients with coeliac disease. Eur. J. Gastroenterol. Hepatol. 10: 641–647.
- Cattell V, Cook T. (1995) The nitric oxide pathway in glomerulonephritis. Curr. Opin. Nephrol. Hypertens. 4: 359–364. · doi:10.1097/00041552-199507000-00013
- Lianos EA. (1998) Activation and potential interactions between the arachidonic acid and l-arginine:nitric oxide pathways in glomerulonephritis. Kidney Int. 53: 540–547. · doi:10.1046/j.1523-1755.1998.00792.x
- Cattell V. (1999) Nitric oxide and glomerulonephritis. Semin. Nephrol. 19: 277–287.
- Wang JS, Tseng HH, Shih DF, et al. (1997) Expression of inducible nitric oxide synthase and apoptosis in human lupus nephritis. Nephron 77: 404–411. · doi:10.1159/000190316
- Vara E, Arias-Diaz J, Garcia C, et al. (1995) Production of TNF alpha, IL-1, IL-6 and nitric oxide by isolated human islets. Transplant. Proc. 27: 3367–3371.
- Pavlovic D, Chen MC, Bouwens L, et al. (1999) Contribution of ductal cells to cytokine responses by human pancreatic islets. Diabetes 48: 29–33. · doi:10.2337/diabetes.48.1.29
- Cortesi R, Ascenzi P, Colasanti M, et al. (1998) Cross-enzyme inhibition by gabexate mesylate: formulation and reactivity study. J. Pharm. Sci. 87: 1335–1340. · doi:10.1021/js980079u
- Wein AJ. (1997) Nitric oxide and interstitial cystitis. J. Urol. 158: 993.
- Bagasra O, Michaels FH, Zheng YM, et al. (1995) Activation of the inducible form of nitric oxide synthase in the brains of patients with multiple sclerosis. Proc. Natl. Acad. Sci. U.S.A. 92: 12041–12045. · DOI · Paper page
- Satoi H, Oka N, Kawasaki T, et al. (1998) Mechanisms of tissue injury in vasculitic neuropathies. Neurology 50: 492–496. · doi:10.1212/wnl.50.2.492
- McKenzie RC, Weller R. (1998) Langerhans cells, keratinocytes, nitric oxide and psoriasis [letter; comment]. Immunol. Today 19: 427–428. · doi:10.1016/s0167-5699(98)01290-0
- Kolb-Bachofen V, Bruch-Gerharz D. (1999) Langerhans cells, nitric oxide, keratinocytes and psoriasis [letter]. Immunol. Today 20: 289. · doi:10.1016/s0167-5699(98)01411-x
- Yamamoto T, Sawada Y, Katayama I, et al. (1998) Increased production of nitric oxide stimulated by interleukin-1beta in peripheral blood mononuclear cells in patients with systemic sclerosis. Br. J. Rheumatol. 37: 1123–1125. · doi:10.1093/rheumatology/37.10.1123
- Clough GF. (1999) Role of nitric oxide in the regulation of microvascular perfusion in human skin in vivo. J. Physiol (Lond) 516: 549–557. · doi:10.1111/j.1469-7793.1999.0549v.x
- Lafond-Walker A, Chen CL, Augustine S, et al. (1997) Inducible nitric oxide synthase expression in coronary arteries of transplanted human hearts with accelerated graft arteriosclerosis. Am. J. Pathol. 151: 919–925.
- Takeichi O, Hayashi M, Tsurumachi T et al. (1999) Inducible nitric oxide synthase activity by interferon-gamma-producing cells in human radicular cysts. Int. Endod. J. 32: 124–130. · doi:10.1046/j.1365-2591.1999.00203.x
- Bacman SR, Berra A, Sterin-Borda L et. al. (1998) Human primary Sjogren’s syndrome autoantibodies as mediators of nitric oxide release coupled to lacrimal gland muscarinic acetylcholine receptors. Curr. Eye Res. 17: 1135–1142. · doi:10.1076/ceyr.17.12.1135.5124
Cited by
Glucagon-like peptide-1 receptor: mechanisms and advances in therapy
Zheng, Z., Zong, Y., Ma, Y., Tian, Y., Pang, Y., Zhang, C., & Gao, J. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01931-z · Cited by 1,036
Changes in Proinflammatory Cytokine Activity after Menopause
Pfeilschifter, J., Köditz, R., Pfohl, M., & Schatz, H. (2002) · Endocrine Reviews · doi:10.1210/edrv.23.1.0456 · Cited by 914
Reactive Oxygen Species Signaling and Oxidative Stress: Transcriptional Regulation and Evolution
Hong, Y., Boiti, A., Vallone, D., & Foulkes, N. S. (2024) · Antioxidants · doi:10.3390/antiox13030312 · Cited by 696
The molecular inflammatory process in aging
Chung, H. Y., Sung, B., Jung, K. J., Zou, Y., & Yu, B. P. (2006) · Antioxidants & Redox Signaling · doi:10.1089/ars.2006.8.572 · Cited by 437
Inducible nitric oxide synthase: Good or bad?
Lind, M., Hayes, A., Caprnda, M., Petrovic, D., Rodrigo, L., Kruzliak, P., & Zulli, A. (2017) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2017.06.036 · Cited by 229
Metadata
- Authors
- Zamora, R., Vodovotz, Y., & Billiar, T. R.
- Venue
- Molecular Medicine
- Published
- 2000-05
- Volume
- 6
- Issue
- 5
- Pages
- 347-373
- ISSN
- 1076-1551 (ISSN-L)
- 1528-3658
- OpenAlex
- W1495576061
- Cited by
- 558
- References
- 310
- FWCI
- 3.59
- Type
- journal article
- Language
- en
- Open access
- gold
- Licence
- www.springernature.com/gp/researchers/text-and-data-mining (tdm)
- www.springernature.com/gp/researchers/text-and-data-mining (vor)
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
How to cite
Cite CoChat for the checks on this page, and the paper for its own findings.
- This page
- CoChat. (2026). Citation check: Inducible Nitric Oxide Synthase and Inflammatory Diseases. https://app.cochat.ai/papers/10.1007/bf03401781
- The paper
- Zamora, R., Vodovotz, Y., & Billiar, T. R. (2000). Inducible Nitric Oxide Synthase and Inflammatory Diseases. Molecular Medicine. https://doi.org/10.1007/bf03401781
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.