Neonatal Cystitis Makes Adult Female Rat Urinary Bladders More Sensitive to Low Concentration Microbial Antigens.

IF 2 Q2 UROLOGY & NEPHROLOGY
Research and Reports in Urology Pub Date : 2023-12-11 eCollection Date: 2023-01-01 DOI:10.2147/RRU.S444167
Ashley C Archer, Jennifer J DeBerry, Cary DeWitte, Timothy J Ness
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引用次数: 0

Abstract

Purpose: Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic pain disorder. Patients with IC/BPS often experience "flares" of symptom exacerbation throughout their lifetime, initiated by triggers, such as urinary tract infections. This study sought to determine whether neonatal bladder inflammation (NBI) alters the sensitivity of adult rat bladders to microbial antigens.

Methods: Female NBI rats received intravesical zymosan treatments on postnatal days P14-P16 while anesthetized; Neonatal Control Treatment (NCT) rats were anesthetized. In adults, bladder and spinal cord Toll-like receptor type 2 and 4 (TLR2, TLR4) contents were determined using ELISAs. Other rats were injected intravesically with lipopolysaccharide (LPS; mimics an E. coli infection; 25, 50, 100, or 200 μg/mL) or Zymosan (mimics yeast infection; 0.01, 0.1, 1, and 10 mg/mL) solutions on the following day. Visceromotor responses (VMRs; abdominal contractions) to graded urinary bladder distention (UBD, 10-60 mm Hg, 20s) were quantified as abdominal electromyograms (EMGs).

Results: Bladder TLR2 and TLR4 protein levels increased in NBI rats. These rats displayed statistically significant, dose-dependent, robustly augmented VMRs following all but the lowest doses of LPS and Zymosan tested, when compared with their adult treatment control groups. The NCT groups showed minimal responses to LPS in adults and minimally increased EMG measurements following the highest dose of Zymosan.

Conclusion: The microbial antigens LPS and Zymosan augmented nociceptive VMRs to UBD in rats that experienced NBI but had little effect on NCT rats at the doses tested. The greater content of bladder TLR2 and TLR4 proteins in the NBI group was consistent with increased responsiveness to their agonists, Zymosan and LPS, respectively. Given that patients with IC/BPS have a higher incidence of childhood urinary tract infections, this increased responsiveness to microbial antigens may explain the flares in symptoms following "subclinical" tract infections.

新生儿膀胱炎使成年雌鼠膀胱对低浓度微生物抗原更敏感
目的:间质性膀胱炎/膀胱疼痛综合征(IC/BPS)是一种慢性疼痛疾病。间质性膀胱炎/膀胱疼痛综合征(IC/BPS)患者在其一生中经常会因尿路感染等诱因而出现症状加重的 "发作"。本研究试图确定新生儿膀胱炎症(NBI)是否会改变成年大鼠膀胱对微生物抗原的敏感性:方法:雌性 NBI 大鼠在麻醉状态下于出生后第 P14 至 P16 天接受膀胱内注射齐莫散治疗;新生儿对照治疗(NCT)大鼠则接受麻醉。成年大鼠的膀胱和脊髓 Toll 样受体 2 型和 4 型(TLR2 和 TLR4)含量通过 ELISAs 检测。次日,给其他大鼠静脉内注射脂多糖(LPS;模拟大肠杆菌感染;25、50、100或200微克/毫升)或Zymosan(模拟酵母菌感染;0.01、0.1、1和10毫克/毫升)溶液。对分级膀胱膨胀(UBD,10-60 毫米汞柱,20 秒)的粘液运动反应(VMRs;腹部收缩)以腹部肌电图(EMGs)进行量化:结果:NBI 大鼠的膀胱 TLR2 和 TLR4 蛋白水平升高。与成人治疗对照组相比,除最低剂量的 LPS 和 Zymosan 外,这些大鼠在所有其他剂量的 LPS 和 Zymosan 测试中都表现出统计学意义上的、剂量依赖性的、强健的 VMRs 增强。NCT 组对成年 LPS 的反应最小,而在使用最高剂量的 Zymosan 后,EMG 测量值的增加最小:结论:微生物抗原 LPS 和 Zymosan 会增强经历过 NBI 的大鼠对UTBD 的痛觉 VMR,但在测试剂量下对 NCT 大鼠影响甚微。在 NBI 组中,膀胱 TLR2 和 TLR4 蛋白的含量更高,这与分别对其激动剂 Zymosan 和 LPS 的反应性增加是一致的。鉴于 IC/BPS 患者儿童尿路感染的发病率较高,这种对微生物抗原反应性的增加可能解释了 "亚临床 "尿路感染后症状发作的原因。
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来源期刊
Research and Reports in Urology
Research and Reports in Urology UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
0.00%
发文量
60
审稿时长
16 weeks
期刊介绍: Research and Reports in Urology is an international, peer-reviewed, open access, online journal. Publishing original research, reports, editorials, reviews and commentaries on all aspects of adult and pediatric urology in the clinic and laboratory including the following topics: Pathology, pathophysiology of urological disease Investigation and treatment of urological disease Pharmacology of drugs used for the treatment of urological disease Although the main focus of the journal is to publish research and clinical results in humans; preclinical, animal and in vitro studies will be published where they will shed light on disease processes and potential new therapies. Issues of patient safety and quality of care will also be considered.
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