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透明质酸、硫酸软骨素及透明质酸-硫酸软骨素联合疗法在间质性膀胱炎动物模型中的比较

Comparison of Intravesical Hyaluronic Acid, Chondroitin Sulfate, and Combination of Hyaluronic Acid-Chondroitin Sulfate Therapies in Animal Model of Interstitial Cystitis.

作者信息

Danacioglu Yavuz Onur, Erol Bulent, Ozkanli Seyma, Yildirim Asif, Atis Ramazan Gokhan, Silay Mesrur Selcuk, Caskurlu Turhan

机构信息

Department of Urology, Istanbul Medeniyet University Faculty of Medicine, Goztepe Training & Research Hospital, Istanbul, Turkey.

Department of Pathology, Istanbul Medeniyet University Faculty of Medicine, Goztepe Training & Research Hospital, Istanbul, Turkey.

出版信息

Int Neurourol J. 2021 Mar;25(1):42-50. doi: 10.5213/inj.1938176.088. Epub 2021 Jan 19.

DOI:10.5213/inj.1938176.088
PMID:33504136
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8022172/
Abstract

PURPOSE

Three intravesical treatment agents were compared in an interstitial cystitis rat model: chondroitin sulfate, hyaluronic acid, and combined hyaluronic acid-chondroitin sulfate.

METHODS

Thirty-five female rats were divided into 5 groups: control (group I), isotonic (group II), chondroitin sulfate (group III), hyaluronic acid (group IV), and hyaluronic acid-chondroitin sulfate (group V). Chemical cystitis was induced in all experimental groups by intravesical instillation of 1 mL of hydrogen peroxide (H2O2) for 15 minutes via the transurethral route. The treatment was administered every other day for 3 sessions 2 days after inducing chemical cystitis. Groups II, III, IV, and V received 1 mL of 0.9% NaCl, 1 mL of 0.2% sodium chondroitin sulfate, 1 mL of low-molecular-weight hyaluronic acid, and 1 mL of 2% sodium chondroitin sulfate+1.6% sodium hyaluronic acid, respectively. On day 7, the animals were sacrificed and the bladders were removed for histopathological and immunohistochemical assessments.

RESULTS

Significant between-group differences were found in vascular congestion (P=0.006). The grade of submucosal edema in groups II and IV was significantly higher than in group I (P=0.006, P=0.006, respectively). In group I, the grade of granulation tissue was lower than the other 4 groups, but no significant difference was found between the remaining groups (P=0.016). Neutrophil cell infiltration was more intense in groups II and IV than in group I (P=0.006, P=0.006, respectively). Significant differences in the leukocyte and mast cell count were detected between groups II and IV (P<0.001, P<0.001, respectively). Abnormal zonula occludens-1 and uroplakin-III immunoreactivity in group II was higher than in groups I, III, or V (P=0.002, P=0.010, respectively). Interleukin-8 expression was lower in group V than in group II (P=0.001).

CONCLUSION

A single treatment of chondroitin sulfate and combined hyaluronic acid-chondroitin sulfate treatment demonstrated efficacy by suppressing inflammation and achieving improvements in the urothelium.

摘要

目的

在间质性膀胱炎大鼠模型中比较三种膀胱内治疗药物:硫酸软骨素、透明质酸以及透明质酸 - 硫酸软骨素组合。

方法

将35只雌性大鼠分为5组:对照组(I组)、等渗组(II组)、硫酸软骨素组(III组)、透明质酸组(IV组)和透明质酸 - 硫酸软骨素组(V组)。通过经尿道途径向所有实验组膀胱内灌注1 mL过氧化氢(H2O2)15分钟诱导化学性膀胱炎。在诱导化学性膀胱炎2天后,每隔一天进行一次治疗,共3个疗程。II组、III组、IV组和V组分别接受1 mL 0.9%氯化钠、1 mL 0.2%硫酸软骨素钠、1 mL低分子量透明质酸和1 mL 2%硫酸软骨素钠 + 1.6%透明质酸钠。在第7天,处死动物并取出膀胱进行组织病理学和免疫组织化学评估。

结果

在血管充血方面发现组间存在显著差异(P = 0.006)。II组和IV组的黏膜下水肿程度显著高于I组(分别为P = 0.006,P = 0.006)。在I组中,肉芽组织等级低于其他4组,但其余组之间未发现显著差异(P = 0.016)。II组和IV组的中性粒细胞浸润比I组更强烈(分别为P = 0.006, P = 0.006)。在II组和IV组之间检测到白细胞和肥大细胞计数存在显著差异(分别为P < 0.001,P < 0.001)。II组中紧密连接蛋白 - 1和尿路上皮蛋白 - III的异常免疫反应性高于I组、III组或V组(分别为P = 0.002,P = 0.010)。V组中白细胞介素 - 8表达低于II组(P = 0.001)。

结论

单次硫酸软骨素治疗以及透明质酸 - 硫酸软骨素联合治疗通过抑制炎症和改善尿路上皮显示出疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/4937a2f4393e/inj-1938176-088f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/3b2aee97aab4/inj-1938176-088f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/040b45a01543/inj-1938176-088f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/1f1be32b4a74/inj-1938176-088f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/709734af6b26/inj-1938176-088f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/4937a2f4393e/inj-1938176-088f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/3b2aee97aab4/inj-1938176-088f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/040b45a01543/inj-1938176-088f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/1f1be32b4a74/inj-1938176-088f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/709734af6b26/inj-1938176-088f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeeb/8022172/4937a2f4393e/inj-1938176-088f5.jpg

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