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. 1994 Dec;62(12):5505–5510. doi: 10.1128/iai.62.12.5505-5510.1994

Moderate stress protects female mice against bacterial infection of the bladder by eliciting uroepithelial shedding.

E Dalal 1, O Medalia 1, O Harari 1, M Aronson 1
PMCID: PMC303295  PMID: 7960132

Abstract

We have previously shown (M. Aronson, O. Medalia, D. Amichay, and O. Nativ, Infect. Immun. 56:1615-1617, 1988) that shedding of viable uroepithelial cells (elicited by invading microorganisms) constitutes an antimicrobial defense mechanism. The present study deals with two different stress-involving procedures, in which increased uroepithelial shedding rendered female mice resistant to vesical infection. Moderate stress was induced in female mice by exposing the animals either to constant illumination for 96 h or to 37 degrees C heat for 24 h. In both cases, the rate of infection was considerably reduced as a result of increased epithelial shedding (P < 0.0001). Stress was manifested by both reduced thymic weight and increased blood corticosterone levels. Shedding was also elicited by intraperitoneal injection of norepinephrine together with hydrocortisone or by intravesical injection of corticosterone. Constant illumination as well as heat enormously facilitated the migration of polymorphonuclear cells into the bladder following the action of chemotactic stimuli. Male mice subjected to identical stress-generating conditions did not display considerable epithelial shedding or increased migration of polymorphonuclear cells, and they were not protected from intravesical infection.

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Selected References

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  1. AMBROSE C. T. THE REQUIREMENT FOR HYDROCORTISONE IN ANTIBODY-FORMING TISSUE CULTIVATED IN SERUM-FREE MEDIUM. J Exp Med. 1964 Jan 1;119:1027–1049. doi: 10.1084/jem.119.6.1027. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Antelman S. M., Kocan D., Knopf S., Edwards D. J., Caggiula A. R. One brief exposure to a psychological stressor induces long-lasting, time-dependent sensitization of both the cataleptic and neurochemical responses to haloperidol. Life Sci. 1992;51(4):261–266. doi: 10.1016/0024-3205(92)90084-3. [DOI] [PubMed] [Google Scholar]
  3. Aronson M., Medalia O., Amichay D., Nativ O. Endotoxin-induced shedding of viable uroepithelial cells is an antimicrobial defense mechanism. Infect Immun. 1988 Jun;56(6):1615–1617. doi: 10.1128/iai.56.6.1615-1617.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Aronson M., Medalia O., Schori L., Mirelman D., Sharon N., Ofek I. Prevention of colonization of the urinary tract of mice with Escherichia coli by blocking of bacterial adherence with methyl alpha-D-mannopyranoside. J Infect Dis. 1979 Mar;139(3):329–332. doi: 10.1093/infdis/139.3.329. [DOI] [PubMed] [Google Scholar]
  5. Labarca C., Paigen K. A simple, rapid, and sensitive DNA assay procedure. Anal Biochem. 1980 Mar 1;102(2):344–352. doi: 10.1016/0003-2697(80)90165-7. [DOI] [PubMed] [Google Scholar]
  6. Orikasa S., Hinman F., Jr Reaction of the vesical wall to bacterial penetration: resistance to attachment, desquamation, and leukocytic activity. Invest Urol. 1977 Nov;15(3):185–193. [PubMed] [Google Scholar]

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