Department of Surgery, Hebei Medical University, Shijiazhuang, Hebei, China.
Department of Urology, Hebei General Hospital, Shijiazhuang, Hebei, China.
Neurourol Urodyn. 2024 Mar;43(3):754-766. doi: 10.1002/nau.25415. Epub 2024 Feb 14.
To explore the effect of blocking galectin-3 in the bladder pain syndrome associated with interstitial cystitis.
A galectin-3 inhibitor was used to treat mice with cyclophosphamide-induced cystitis. The expression of galectin-3 in bladder tissues and urine was examined by immunohistochemistry and enzyme-linked immunosorbent assay (ELISA), respectively. Suprapubic-pelvic pain, bladder voiding, bladder pain-like nociceptive behavior, and referred hyperalgesia were assessed. The weights of the bladders were also measured, and inflammatory cell infiltration and inflammatory cytokine levels were examined by histopathological evaluation. The inflammatory cytokines interleukin 1β (IL-1β), nerve growth factor (NGF), IL-6, and tumor necrosis factor α (TNF-α) were measured by ELISA.
Increases in galectin-3 levels, inflammation, bladder weight, and bladder pain-related symptoms were observed in bladders with cyclophosphamide-induced cystitis. Administration of the galectin-3 inhibitor significantly mitigated bladder pain-related symptoms and inflammatory response. In response to the 500 μM dose of the galectin-3 inhibitor, nociceptive behaviors, nociceptive score, and bladder-to-body weight ratios were reduced by 65.1%, 65.3%, and 40.3%, respectively, while 500 μM Gal-3 inhibitor increased pelvic pain threshold by 86.7%. Moreover, galectin-3 inhibitor treatment inhibited the inflammation. Compared to untreated CYP-induced mice, there were significant changes in the levels of IL-1β (41.72 ± 2.05 vs. 18.91 ± 2.26 pg/mg tissues), NGF (9.64 ± 0.38 vs. 1.88 ± 0.05 pg/mg tissues), IL-6 (42.67 + 1.51 vs. 21.26 + 2.78 pg/mg tissues, and TNF-α (22.02 ± 1.08 vs. 10.70 ± 0.80 pg/mg tissues) in response to the highest dose of the Gal-3 inhibitor subgroup (500 μM), and 500 μM Gal-3 inhibitor reduced mast cell infiltration ratios by 71.8%.
The galectin-3 inhibitor relieved pelvic pain, urinary symptoms, and bladder inflammation in mice with cyclophosphamide-induced cystitis. Thus, galectin-3 inhibitors may be novel agents in interstitial cystitis treatment.
探讨阻断半乳糖凝集素-3对伴发间质性膀胱炎的膀胱疼痛综合征的作用。
用半乳糖凝集素-3 抑制剂治疗环磷酰胺诱导的膀胱炎小鼠。通过免疫组化和酶联免疫吸附试验(ELISA)分别检测膀胱组织和尿液中半乳糖凝集素-3 的表达。评估耻骨上-骨盆疼痛、膀胱排空、膀胱疼痛样伤害感受行为和牵涉性痛觉过敏。还测量了膀胱的重量,并通过组织病理学评估检查炎症细胞浸润和炎症细胞因子水平。通过 ELISA 测定白细胞介素 1β(IL-1β)、神经生长因子(NGF)、IL-6 和肿瘤坏死因子α(TNF-α)等炎症细胞因子。
在环磷酰胺诱导的膀胱炎的膀胱中观察到半乳糖凝集素-3 水平升高、炎症、膀胱重量和与膀胱疼痛相关的症状。给予半乳糖凝集素-3 抑制剂可显著减轻与膀胱疼痛相关的症状和炎症反应。对于 500μM 半乳糖凝集素-3 抑制剂剂量,伤害感受行为、伤害感受评分和膀胱与体重比分别降低 65.1%、65.3%和 40.3%,而 500μM Gal-3 抑制剂使骨盆疼痛阈值增加 86.7%。此外,半乳糖凝集素-3 抑制剂治疗抑制了炎症。与未治疗的 CYP 诱导的小鼠相比,IL-1β(41.72±2.05 与 18.91±2.26 pg/mg 组织)、NGF(9.64±0.38 与 1.88±0.05 pg/mg 组织)、IL-6(42.67+1.51 与 21.26+2.78 pg/mg 组织)和 TNF-α(22.02±1.08 与 10.70±0.80 pg/mg 组织)的水平有显著变化,半乳糖凝集素-3 抑制剂亚组(500μM)的最高剂量,500μM Gal-3 抑制剂使肥大细胞浸润率降低 71.8%。
半乳糖凝集素-3 抑制剂缓解了环磷酰胺诱导的膀胱炎小鼠的骨盆疼痛、尿路症状和膀胱炎症。因此,半乳糖凝集素-3 抑制剂可能成为治疗间质性膀胱炎的新药物。