Nitric oxide in parasitic infections: a friend or foe?

被引:4
作者
Omar M. [1 ]
Abdelal H.O. [2 ]
机构
[1] Department of Medical Parasitology, Faculty of Medicine, Zagazig University, Gameyet Almohafza St. 1, Menya Al-Kamh, Sharkia Governorate, City of Zagazig
[2] LIS: Cross-National Data Center, Maison des Sciences Humaines - 5e étage, 11- porte des Sciences, Esch-Belval
关键词
Immune response; Isoenzymes; Nitric oxide; Nitric oxide synthase; Parasitic infections;
D O I
10.1007/s12639-022-01518-x
中图分类号
学科分类号
摘要
The complex interaction between the host and the parasite remains a puzzling question. Control of parasitic infections requires an efficient immune response that must be balanced against destructive pathological consequences. Nitric oxide is a nitrogenous free radical which has many molecular targets and serves diverse functions. Apart from being a signaling messenger, nitric oxide is critical for controlling numerous infections. There is still controversy surrounding the exact role of nitric oxide in the immune response against different parasitic species. It proved protective against intracellular protozoa, as well as extracellular helminths. At the same time, it plays a pivotal role in stimulating detrimental pathological changes in the infected hosts. Several reports have discussed the anti-parasitic and immunoregulatory functions of nitric oxide, which could directly influence the control of the infection. Nevertheless, there is scarce literature addressing the harmful cytotoxic impacts of this mediator. Thus, this review provides insights into the most updated concepts and controversies regarding the dual nature and opposing sides of nitric oxide during the course of different parasitic infections. © 2022, Indian Society for Parasitology.
引用
收藏
页码:1147 / 1163
页数:16
相关论文
共 147 条
  • [1] Abdel Aziz M., Elsayed H., Insights into the effects of inducible and neuronal nitric oxide synthase isoenzymes in experimental intestinal heterophyiasis, PUJ, 14, pp. 86-94, (2021)
  • [2] Abd-Elhamid T.H., Abdel-Rahman I.A.M., Mahmoud A.R., Allemailem K.S., Almatroudi A., Fouad S.S., Abdella O.H., Elshabrawy H.A., El-Kady A.M., A Complementary herbal product for controlling giardiasis, Antibiotics (basel), 10, (2021)
  • [3] Abdeltawab M., Abdel-Shafi I., Aboulhoda B., Wanas H., Saad El-Din S., Amer S., Hamed A., Investigating the effect of the nitric oxide donor L-arginine on albendazole efficacy in Trichinella spiralis-induced myositis and myocarditis in mice, PUJ, 15, pp. 60-70, (2022)
  • [4] Adams L.B., Hibbs J.B., Taintor R.R., Krahenbuhl J.L., Microbiostatic effect of murine-activated macrophages for Toxoplasma gondii. Role for synthesis of inorganic nitrogen oxides from L-arginine, J Immunol, 144, pp. 2725-2729, (1990)
  • [5] Ahmed S.F., Oswald I.P., Caspar P., Hieny S., Keefer L., Sher A., James S.L., Developmental differences determine larval susceptibility to nitric oxide mediated killing in a murine model of vaccination against Schistosoma mansoni, Infect Immun, 65, pp. 219-226, (1997)
  • [6] Alexander J., Scharton-Kersten T.M., Yap G., Roberts C.W., Liew F.Y., Sher A., Mechanisms of Innate Resistance to Toxoplasma gondii Infection, Philos Trans R Soc Lond B Biol Sci, 352, pp. 1355-1359, (1997)
  • [7] Anand N., Lutshumba J., Whitlow M., Abdelaziz M.H., Mani R., Suzuki Y., Deficiency in indoleamine-2, 3-dioxygenase induces upregulation of guanylate binding protein 1 and inducible nitric oxide synthase expression in the brain during cerebral infection with Toxoplasma gondii in genetically resistant BALB/c mice but not in genetically susceptible C57BL/6 mice, Microbes Infect, 12, (2021)
  • [8] Andersen Y.S., Gillin F.D., Eckmann L., Adaptive immunity-dependent intestinal hypermotility contributes to host defense against Giardia spp, Infect Immun, 74, pp. 2473-2476, (2006)
  • [9] Anstey N.M., Weinberg J.B., Hassanali M.Y., Mwaikambo E.D., Manyenga D., Misukonis M.A., Arnelle D.R., Hollis D., McDonald M.I., Granger D.L., Nitric oxide in Tanzanian children with malaria: Inverse relationship between malaria severity and nitric oxide production/nitric oxide synthase type 2 expression, J Exp Med, 184, pp. 557-567, (1996)
  • [10] Anthony R.M., Rutitzky L.I., Urban J.F., Stadecker M.J., Gause W.C., Protective immune mechanisms in helminth infection, Nat Rev Immunol, 12, pp. 975-987, (2007)