Role of substance P in several models of bladder inflammation

被引:38
作者
Luber-Narod, J
Austin-Ritchie, T
Hollins, C
Menon, M
Malhotra, RK
Baker, S
Carraway, RE
机构
[1] Univ Massachusetts, Sch Med, Dept Surg, Worcester, MA 01655 USA
[2] Cambridge Biosci, Worcester, MA USA
[3] BASF Inc, Worcester, MA USA
[4] Univ Massachusetts, Med Ctr, Dept Pathol, Worcester, MA USA
[5] Univ Massachusetts, Med Ctr, Dept Informat & Res, Worcester, MA USA
[6] Univ Massachusetts, Med Ctr, Dept Cellular & Mol Physiol, Worcester, MA USA
来源
UROLOGICAL RESEARCH | 1997年 / 25卷 / 06期
关键词
interstitial cystitis; bladder inflammation; substance P; animal models;
D O I
10.1007/BF01268854
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Substance P (SP) is a peptide found in the sensory nervous system which has multiple biologic effects including stimulation of muscle contraction, pain nociception, immune cell functions, plasma extravasation and a constellation of inflammatory effects. Here we investigate the role of SP in several animals models of bladder inflammation. Using the female Lewis rat, inflammation was induced using either xylene, lipopolysaccharide (LPS) or polyinosinic-polycytidylic acid (polyIC). Inflammation occurred rapidly (4 h) and was maintained in each model for at least 7 days. Each of these protocols decreased the bladder content of immunoreactive SP by approximately 50%, suggesting enhanced release. There was no change in the urinary frequency of these animals over 3 weeks, suggesting that urinary frequency changes are not mediated by acute inflammation. We also found that the SP receptor (NK1) antagonist, (-)CP96345, was unable to block the inflammation produced by polyIC, suggesting that SP is not an obligatory mediator of immune cell stimulation in this model.
引用
收藏
页码:395 / 399
页数:5
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