Potentilla chinensis aqueous extract attenuates cyclophosphamide-induced hemorrhagic cystitis in rat model

被引:5
|
作者
Juszczak, Kajetan [1 ]
Adamowicz, Jan [2 ]
Zapala, Lukasz [3 ]
Kluz, Tomasz [4 ]
Adamczyk, Przemyslaw [5 ]
Wdowiak, Artur [6 ]
Bojar, Iwona [7 ]
Misiek, Marcin [8 ]
Grzybowska, Magdalena Emilia [9 ]
Stangel-Wojcikiewicz, Klaudia [10 ]
Poleszak, Ewa [11 ]
Pokrywczynska, Marta [2 ]
Drewa, Tomasz [1 ]
Wrobel, Andrzej [12 ]
机构
[1] Nicolaus Copernicus Univ, Coll Med, Dept Urol & Androl, Skfodowskiej 9, PL-85094 Bydgoszcz, Poland
[2] Nicolaus Copernicus Univ, Coll Med, Dept Regenerat Med, Bydgoszcz, Poland
[3] Med Univ Warsaw, Clin Gen Oncol & Funct Urol, Warsaw, Poland
[4] Rzeszow Univ, Inst Med Sci, Dept Gynecol & Obstet, Med Coll, Rzeszow, Poland
[5] Nicolaus Copernicus Hosp, Dept Gen & Oncol Urol, Torun, Poland
[6] Med Univ Lublin, Fac Hlth Sci, Chair Obstet & Gynecol, Lublin, Poland
[7] Inst Rural Hlth Lublin, Dept Womens Hlth, Lublin, Poland
[8] Holy Cross Canc Ctr, Dept Gynecol Oncol, Kielce, Poland
[9] Med Univ Gdansk, Dept Gynecol Gynecol Oncol & Gynecol Endocrinol, Gdansk, Poland
[10] Jagiellonian Univ Med Coll, Dept Gynecol & Oncol, Krakow, Poland
[11] Med Univ Lublin, Chair & Dept Appl & Social Pharm, Lab Preclin Testing, Lublin, Poland
[12] Med Univ Lublin, Dept Gynaecol 2, Jaczewskiego 8, PL-20954 Lublin, Poland
关键词
URINARY-BLADDER; RHO KINASE; MESNA; IDENTIFICATION; ANTIOXIDANT; ALPHA;
D O I
10.1038/s41598-022-17393-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cyclophosphamide (CYP) damages all mucosal defence lines and induces hemorrhagic cystitis (HC) leading to detrusor overactivity. Patients who undergo combined chemio-radiotherapy are at higher risk of HC. Potentilla chinensis extract (PCE) prevent oxidative stress-dependent diseases. Thus, the aim of the study was to investigate the effect of PCE on urinary bladder function in CYP-induced HC in preclinical study. 60 rats were divided into 4 groups, as follows: I-control, II-rats with CYP-induced HC, III-rats received PCE in dose of 500 mg/kg, and IV-rats with CYP-induced HC which received PCE in dose of 500 mg/kg. PCE or vehicle were administered orally for 14 days. The cystometry was performed 3 days after the last dose of the PCE. Next, urothelium thickness and oedema measurement and biochemical analyses were performed. Cyclophosphamide induced hemorrhagic cystitis. PCE had no influence on the urinary bladder function and micturition cycles in normal rats. PCE diminished the severity of CYP-induced hemorrhagic cystitis. In the urothelium the cyclophosphamide induced the elevation of CGRP, TNF-alpha, IL-6, IL-1 beta, OTC3, NIT, and MAL. Also, the level of T-H protein, HB-EGF, and ZO1 was decreased. Moreover, the level of ROCK1 and VAChT in detrusor muscle increased. cyclophosphamide caused an increased concentration of BDNF and NGF in the urine. In turn, PCE in cyclophosphamide-induced hemorrhagic cystitis caused a reversal of the described biochemical changes within urothelium, detrusor muscle and urine. PCE attenuates detrusor overactivity. In conclusion, our results revealed that PCE attenuates detrusor overactivity in case of cyclophosphamide-induced hemorrhagic cystitis. The potential properties of PCE appear to be important in terms of preventing of oxidative stress-dependent dysfunction of urinary bladder. PCE may become a potential supportive treatment in patient to whom cyclophosphamide-based chemotherapy is used.
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页数:13
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