The serotonin(5-HT)2A receptor is involved in the hypersensitivity of bladder afferent neurons in cyclophosphamide-induced cystitis

被引:1
|
作者
Chen, Xun [1 ]
Lv, Rong [1 ]
Li, Mingzhuo [1 ]
Zhang, Lin [1 ]
Sun, Yudong [1 ]
Cao, Nailong [1 ]
Gu, Baojun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Peoples Hosp 6, Sch Med, Dept Urol, 600 Yishan Rd, Shanghai 200233, Peoples R China
基金
中国国家自然科学基金;
关键词
5-Hydroxytryptamine receptors; Bladder overactivity; Hyperalgesia; Sensory neurons; Calcium homeostasis; PERIPHERAL 5-HT2A RECEPTOR; OUTLET OBSTRUCTION; TACTILE ALLODYNIA; UP-REGULATION; PAIN; EXPRESSION; TRPV1; MICTURITION; INJURY; HYPEREXCITABILITY;
D O I
10.1016/j.ejphar.2024.176909
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Interstitial cystitis/bladder pain syndrome (IC/BPS) is a chronic bladder inflammation characterized by the main symptoms of urinary frequency, urgency, and pelvic pain. The hypersensitivity of bladder afferent neurons is considered a significant pathophysiologic mechanism in IC/PBS. Serotonin (5-HT, 5-hydroxytryptamine) receptors are known to be involved in the regulation of the micturition reflex and hyperalgesia, but the effect of 5HT receptors on cystitis remains unknown. In this study, a rat model of interstitial cystitis induced by intraperitoneal injection of cyclophosphamide (CYP) was used to investigate the role of 5-HT receptors on cystitis. The histology and urodynamics exhibited chronic cystitis and overactive bladder in CYP-treated rats. Notably, among 5-HT1A, 5-HT2A and 5-HT7 receptors, the expression of 5-HT2A receptor was significantly increased in bladder afferent neurons in CYP-treated rats. Intrathecal administration of the 5-HT2A receptor antagonist M100907 could alleviate bladder overactivity and hyperalgesia in CYP-induced cystitis rats. Neuronal calcium imaging of bladder afferent neurons revealed increased calcium influx induced by the 5-HT2A receptor agonist or capsaicin in cystitis rats, which could be inhibited by M100907. Moreover, RNA sequencing indicated that differentially expressed genes were enriched in inflammation-related pathways and cellular calcium homeostasis. These findings suggest that the 5-HT2A receptor is involved in the hypersensitivity of bladder afferent neurons in CYP-induced cystitis, and M100907 could alleviate bladder overactivity and hyperalgesia in CYP-induced cystitis by inhibiting neuronal hypersensitivity in the afferent pathways. The 5-HT2A receptor may be a potential therapeutic target for the treatment of IC/BPS.
引用
收藏
页数:15
相关论文
共 44 条
  • [41] Valproate reverses stress-induced somatic hyperalgesia and visceral hypersensitivity by up-regulating spinal 5-HT2C receptor expression in female rats
    Xu, Gang -Zhu
    Xue, Yang
    Wei, Si-Qi
    Li, Jia-Heng
    Traub, Richard J.
    Wang, Mao-De
    Cao, Dong-Yuan
    NEUROPHARMACOLOGY, 2020, 165
  • [42] Serotonin transporter inhibition and 5-HT2C receptor activation drive loss of cocaine-induced locomotor activation in DAT Val559 mice
    Stewart, Adele
    Davis, Gwynne L.
    Gresch, Paul J.
    Katamish, Rania M.
    Peart, Rodeania
    Rabil, Maximilian J.
    Gowrishankar, Raajaram
    Carroll, F. Ivy
    Hahn, Maureen K.
    Blakely, Randy D.
    NEUROPSYCHOPHARMACOLOGY, 2019, 44 (05) : 994 - 1006
  • [43] Agomelatine, a MT1/MT2 melatonergic receptor agonist with serotonin 5-HT2C receptor antagonistic properties, suppresses Prevotella intermedia lipopolysaccharide-induced production of proinflammatory mediators in murine macrophages
    Hyeon, Jin-Yi
    Choi, Eun-Young
    Choe, So-Hui
    Park, Hae Ryoun
    Choi, Jeom-Il
    Choi, In Soon
    Kim, Sung-Jo
    ARCHIVES OF ORAL BIOLOGY, 2017, 82 : 11 - 18
  • [44] Effect of Selective Serotonin (5-HT)2B Receptor Agonist BW723C86 on Epidermal Growth Factor/Transforming Growth Factor-α Receptor Tyrosine Kinase and Ribosomal p70 S6 Kinase Activities in Primary Cultures of Adult Rat Hepatocytes
    Naito, Kota
    Kurihara, Kazuki
    Moteki, Hajime
    Kimura, Mitsutoshi
    Natsume, Hideshi
    Ogihara, Masahiko
    BIOLOGICAL & PHARMACEUTICAL BULLETIN, 2019, 42 (04) : 631 - 637