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Journal of Pharmacology and Experimental Therapeutics

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OtherRENAL PHARMACOLOGY

Bladder Instillation and Intraperitoneal Injection ofEscherichia coli Lipopolysaccharide Up-regulate Cytokines and iNOS in Rat Urinary Bladder

Lief Eric Olsson, Marcia A. Wheeler, William C. Sessa and Robert M. Weiss
Journal of Pharmacology and Experimental Therapeutics March 1998, 284 (3) 1203-1208;
Lief Eric Olsson
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Marcia A. Wheeler
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William C. Sessa
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Robert M. Weiss
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Abstract

Systemic bacterial lipopolysaccharides (LPS) induce inflammatory responses characteristic of sepsis. Instillation of LPS into rat bladder produces a localized inflammatory response similar to that seen in urinary tract infections (UTIs). Four hours after intravesical instillation of LPS, neutrophils infiltrate into the bladder, and mRNA for inducible nitric oxide synthase (iNOS) and the cytokines, interleukin (IL)-6 and IL-10, is detected in rat bladder but not in the kidney. Induction of iNOS protein is inferred because urinary nitrate and cGMP levels are increased 4 hr after LPS intravesical instillation and remain elevated for at least 24 hr. When LPS is injected intraperitoneally, iNOS and IL-6 mRNA are induced both in the bladder and in the kidney. These data are consistent with the effects of intravesical instillation of LPS remaining localized. iNOS activity increases in both particulate and soluble bladder fractions when measured 4 hr after intravesical instillation of LPS. The magnitude of these increases in iNOS activity in the bladder is not as great as when LPS is injected intraperitoneally. Intravesical instillation of LPS induces no increase in lung or kidney NOS activity. The localized inflammatory response produced by intravesical instillation of LPS demonstrates the importance of LPS as a mediator of the host response in UTIs and supports the use of urinary measurements of nitrate and cGMP in humans as indicative of the localized induction of iNOS in UTIs.

Footnotes

  • Send reprint requests to: Robert M. Weiss, Section of Urology, Yale University School of Medicine, 333 Cedar Street, P.O. Box 208041, New Haven CT 06520-8041.

  • ↵1 Supported in part by Public Health Service DK38311 and DK47548 from the National institute of Diabetes and Digestive and Kidney Diseases.

  • Abbreviations:
    b.p.
    base pair
    EGTA
    ethyleneglycol-bis(β-aminoethyl ether)-N,N,N′,N′-tetraacetic acid
    FAD
    flavin adenine dinucleotide
    iNOS
    inducible nitric oxide synthase
    HEPES
    N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid
    IL
    interleukin
    l-NMMA
    NG-monomethyl-l-arginine
    LPS
    lipopolysaccharide
    NOS
    nitric oxide synthase
    NOx
    nitrate plus nitrite
    PBS
    phosphate-buffered saline
    RT-PCR
    reverse transcription polymerase chain reaction
    TNF
    tumor necrosis factor
    UTI
    urinary tract infection
    • Received August 12, 1997.
    • Accepted November 14, 1997.
  • The American Society for Pharmacology and Experimental Therapeutics
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Journal of Pharmacology and Experimental Therapeutics
Vol. 284, Issue 3
1 Mar 1998
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OtherRENAL PHARMACOLOGY

Bladder Instillation and Intraperitoneal Injection ofEscherichia coli Lipopolysaccharide Up-regulate Cytokines and iNOS in Rat Urinary Bladder

Lief Eric Olsson, Marcia A. Wheeler, William C. Sessa and Robert M. Weiss
Journal of Pharmacology and Experimental Therapeutics March 1, 1998, 284 (3) 1203-1208;

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OtherRENAL PHARMACOLOGY

Bladder Instillation and Intraperitoneal Injection ofEscherichia coli Lipopolysaccharide Up-regulate Cytokines and iNOS in Rat Urinary Bladder

Lief Eric Olsson, Marcia A. Wheeler, William C. Sessa and Robert M. Weiss
Journal of Pharmacology and Experimental Therapeutics March 1, 1998, 284 (3) 1203-1208;
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