The effect of sex hormones on progression of Leishmania donovani infection in liver and spleen of BALB/c mice

https://doi.org/10.53730/ijhs.v6nS3.7404

Authors

  • Moayad Mijbil Ubaid Department of Science, College of Basic Education, University of Sumer, Iraq
  • Jassim Hameed Rahma Department of Biology, College of Education for girls, University of Kufa, Iraq

Keywords:

sex hormones, estradiol, testosterone, visceral leishmaniasis, Leishmania donovani, hepatosplenomegaly

Abstract

Leishmania donovani invades and resides within tissue macrophages in the spleen, liver, and bone marrow leading to a histological change such as hepatosplenomegaly. In the present study we experimented the effect of gender and sex hormones on the progression of the visceral leishmaniasis disease in the liver and the spleen of BALB/c mice. The mice were divided into two groups, males and females, then male group was divided into three sub groups, first injected normal saline (control), the second injected with 107 promastigotes intraperitonially and the third injected with 107 promastigotes intraperitonially plus estradiol subcutaneously. Female group was divided into three groups, the first injected with normal saline, the second injected with 107 promastigotes and the third injected with 107 promastigotes intraperitonially plus testosterone subcutaneously. After six weeks, all animals were sacrificed and dissected then liver and spleen were removed, weighted and histological sections were made from them. 

Downloads

Download data is not yet available.

References

Klein SL. The effects of hormones on sex differences in infection:from genes to behavior. Neurosci Biobehav Rev 2000; 24: 627–638.

Roberts CW, Walker W & Alexander J. Sex-associated hormones and immunity to protozoan parasites. Clin Microbiol Rev 2001; 14 (3): 476–488.

Zuk M & McKean KA. Sex differences in parasite infections: patterns and processes. Int J Parasitol 1996; 26: 1009–1023. Klein SL. The effects of hormones on sex differences in infection: from genes to behavior. Neurosci Biobehav Rev 2000; 24: 627–638.

Wizemann TM, Pardue M, eds. Exploring the Biological Contributions to Human Health: Does Sex Matter?. Washington DC: National Academy Press, 2001.

Kumar, R., and Nyle´ n, S. (2012). Immunobiology of visceral leishmaniasis. Front. Immunol. 3, 251.

Zhang, G., Zhong, J., Wang, T., & Zhong, L. (2020). A case of visceral leishmaniasis found by left oblique hernia: A case report Corrigendum in /10.3892/etm.2020.9477. Experimental and Therapeutic Medicine, 19, 2697-2701. https://doi.org/10.3892/etm.2020.8487

Poulaki, A., Piperaki, E. T., & Voulgarelis, M. (2021). Effects of Visceralising Leishmania on the Spleen, Liver, and Bone Marrow: A Pathophysiological Perspective. Microorganisms, 9(4), 759. https://doi.org/10.3390/microorganisms9040759

Bankoti, R.; Stager, S. Differential Regulation of the Immune Response in the Spleen and Liver of Mice Infected with Leishmania donovani. J. Trop. Med. 2012, 2012, 639304.

Hermida, M.D.; de Melo, C.V.B.; Lima, I.D.S.; Oliveira, G.G.S.; Dos-Santos, W.L.C. Histological Disorganization of Spleen Compartments and Severe Visceral Leishmaniasis. Front. Cell. Infect. Microbiol. 2018, 8, 394.

Salguero, F. J., Garcia-Jimenez, W. L., Lima, I., & Seifert, K. (2018). Histopathological and immunohistochemical characterisation of hepatic granulomas in Leishmania donovani-infected BALB/c mice: a time-course study. Parasites & vectors, 11(1), 73. https://doi.org/10.1186/s13071-018-2624-z

Kaye, P. M., & Beattie, L. (2016). Lessons from other diseases: granulomatous inflammation in leishmaniasis. Seminars in immunopathology, 38(2), 249–260. https://doi.org/10.1007/s00281-015-0548-7

Kaye, P. M., Svensson, M., Ato, M., Maroof, A., Polley, R., Stager, S., Zubairi, S., & Engwerda, C. R. (2004). The immunopathology of experimental visceral leishmaniasis. Immunological reviews, 201, 239–253. https://doi.org/10.1111/j.0105-2896.2004.00188.x

Kima PE. PI3K signaling in Leishmania infections. Cell Immunol. 2016 Nov;309:19-22. doi: 10.1016/j.cellimm.2016.09.004. Epub 2016 Sep 7. PMID: 27622385; PMCID: PMC5127740.

Fischer, A. H., Jacobson, K. A., Rose, J., & Zeller, R. (2008). Hematoxylin and eosin staining of tissue and cell sections. CSH protocols, 2008, pdb.prot4986. https://doi.org/10.1101/pdb.prot4986

Morimoto, A., Omachi, S., Osada, Y., Chambers, J. K., Uchida, K., Sanjoba, C., Matsumoto, Y., & Goto, Y. (2016). Hemophagocytosis in Experimental Visceral Leishmaniasis by Leishmania donovani. PLoS neglected tropical diseases, 10(3), e0004505. https://doi.org/10.1371/journal.pntd.0004505

16- Burza, S., Croft, S. L., & Boelaert, M. (2018). Leishmaniasis. Lancet (London, England), 392(10151), 951–970. https://doi.org/10.1016/S0140-6736(18)31204-2

Martinez de Narvajas, I., Díaz, A., Bassegoda, O., Carpio, A., Fuster, C., Valls, M. E., Alvarez-Martínez, M. J., García-Vidal, C., Soriano, A., Martínez, J. A., & Ambrosioni, J. (2019). Acute liver failure due to visceral leishmaniasis in Barcelona: a case report. BMC infectious diseases, 19(1), 874. https://doi.org/10.1186/s12879-019-4553-7

Ramzy, U. & Zghair, K. (2020). Histological disturbance in liver and spleen of visceral leishmaniasis infected mice with the progression of infection. biochemical and Cellular Archives. 20. 0-000.

Maeda, K.; Sadoughi, S.; Morimoto, A.; Uchida, K.; Chambers, J.K.; Sanjoba, C.; Yamagishi, J.; Goto, Y. (2021). Hepatomegaly Associated with Non-Obstructive Sinusoidal Dilation in Experimental Visceral Leishmaniasis. Pathogens , 10(11),1356. https://doi.org/10.3390/pathogens10111356

Kennedy, A. D., & DeLeo, F. R. (2009). Neutrophil apoptosis and the resolution of infection. Immunologic research, 43(1-3), 25–61. https://doi.org/10.1007/s12026-008-8049-6

Reis, A. B., Martins-Filho, O. A., Teixeira-Carvalho, A., Giunchetti, R. C., Carneiro, C. M., Mayrink, W., Tafuri, W. L., & Corrêa-Oliveira, R. (2009). Systemic and compartmentalized immune response in canine

AL–Azawy, Afrah Ali Abd–Alamer (2017). The Impact of diabetes and Pentostam on development the infected Leishmania donovani parasite in male laboratory mice. M.Sc. thesis, Thi-qar University ,College of Education for Pure Science, Biology Department, 125pages.

Reimer, K. A., & Ideker, R. E. (1987). Myocardial ischemia and infarction: anatomic and biochemical substrates for ischemic cell death and ventricular arrhythmias. Human pathology, 18(5), 462–475. https://doi.org/10.1016/s0046-8177(87)80031-x

Bonventre J. V. (1993). Mechanisms of ischemic acute renal failure. Kidneyinternational, 43(5),11601178.https://doi.org/10.1038/ki.1993.163

Beattie, L., Peltan, A., Maroof, A., Kirby, A., Brown, N., Coles, M., Smith, D. F., & Kaye, P. M. (2010). Dynamic imaging of experimental Leishmania donovani-induced hepatic granulomas detects Kupffer cell-restricted antigen presentation to antigen-specific CD8 T cells. PLoS pathogens, 6(3), e1000805. https://doi.org/10.1371/journal.ppat.1000805

Veress, B., Omer, A., Satir, A. A., & El Hassan, A. M. (1977). Morphology of the spleen and lymph nodes in fatal visceral leishmaniasis. Immunology, 33(5), 605–610.

Snider, H., Lezama-Davila, C., Alexander, J., & Satoskar, A. R. (2009). Sex hormones and modulation of immunity against leishmaniasis. Neuroimmunomodulation, 16(2), 106–113. https://doi.org/10.1159/000180265

Esfandiari, F., Sarkari, B., Turki, H., Arefkhah, N., & Shakouri, N. (2019). Level of circulating steroid hormones in malaria and cutaneous leishmaniasis: a case control study. Journal of parasitic diseases : official organ of the Indian Society for Parasitology, 43(1), 54–58. https://doi.org/10.1007/s12639-018-1055-2

GBD. Global, regional, and national age-sex- specific mortality for 282 causes of death in 195 countries and territories, 1980-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. 2018;392(10159):1736-1788.

Olsen, N. J., & Kovacs, W. J. (1996). Gonadal steroids and immunity. Endocrine reviews, 17(4), 369–384. https://doi.org/10.1210/edrv-17-4-369

Notas, G., Kampa, M., & Castanas, E. (2020). G Protein-Coupled Estrogen Receptor in Immune Cells and Its Role in Immune-Related Diseases. Frontiers in endocrinology, 11, 579420. https://doi.org/10.3389/fendo.2020.579420

Hellberg, S., Raffetseder, J., Rundquist, O., Magnusson, R., Papapavlou, G., Jenmalm, M. C., Ernerudh, J., & Gustafsson, M. (2021). Progesterone Dampens Immune Responses in In Vitro Activated CD4+ T Cells and Affects Genes Associated With Autoimmune Diseases That Improve DuringPregnancy. Frontiersinimmunology, 12,672168.https://doi.org/10.3389/fimmu.2021.672168

Gubbels Bupp, M. R., & Jorgensen, T. N. (2018). Androgen-Induced Immunosuppression. Frontiers in immunology, 9, 794. https://doi.org/10.3389/fimmu.2018.00794

Rodríguez, N. E., Lima, I. D., Gaur Dixit, U., Turcotte, E. A., Lockard, R. D., Batra-Sharma, H., Nascimento, E. L., Jeronimo, S., & Wilson, M. E. (2018). Epidemiological and Experimental Evidence for Sex-Dependent Differences in the Outcome of Leishmania infantum Infection. The American journal of tropical medicine and hygiene, 98(1), 142–145. https://doi.org/10.4269/ajtmh.17-0563

Romano, A., Brown, N., Ashwin, H., Doehl, J., Hamp, J., Osman, M., Dey, N., Rani, G. F., Ferreira, T. R., & Kaye, P. M. (2021). Interferon-γ-Producing CD4+ T Cells Drive Monocyte Activation in the Bone Marrow During Experimental Leishmania donovani Infection. Frontiers in immunology, 12, 700501. https://doi.org/10.3389/fimmu.2021.700501

Samant, M., Sahu, U., Pandey, S. C., & Khare, P. (2021). Role of Cytokines in Experimental and Human Visceral Leishmaniasis. Frontiers in cellular and infection microbiology, 11, 624009. https://doi.org/10.3389/fcimb.2021.624009

Published

16-05-2022

How to Cite

Ubaid, M. M., & Rahma, J. H. (2022). The effect of sex hormones on progression of Leishmania donovani infection in liver and spleen of BALB/c mice. International Journal of Health Sciences, 6(S3), 6327–6337. https://doi.org/10.53730/ijhs.v6nS3.7404

Issue

Section

Peer Review Articles