MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1155/2021/4009308

Медицинская библиотека · Oxidative medicine and cellular longevity · 2021

Nrf2 Pathway Ameliorates Bladder Dysfunction in Cyclophosphamide-Induced Cystitis via Suppression of Oxidative Stress.

Ni Bin, Chen Zhengsen, Shu Le, Shao Yunpeng, Huang Yi, Tamrat Nebiyu Elias, Wei Zhongqing, Shen Baixin

СтатьяПеревод в очереди

Аннотация

OBJECTIVE

To investigate the protective effect and molecular mechanism of nuclear factor E2-related factor 2 (Nrf2) pathway in interstitial cystitis (IC).

METHODS

We established a mouse model of IC by cyclophosphamide (CYP) in wild-type mice and Nrf2 gene knockout mice. We examined the histological and functional alterations, the changes of oxidative stress markers, and the expression of the antioxidant genes downstream of Nrf2 pathway.

RESULTS

After CYP administration, the mice showed urinary frequency and urgency, pain sensitization, decreased contractility, bladder edema, and oxidative stress disorder. Notably, the Nrf2-/- CYP mice had more severe symptoms. The mRNA and protein levels of antioxidant genes downstream of Nrf2 pathway were significantly upregulated in the Nrf2+/+ CYP mice, while there were no significant changes in the Nrf2-/- CYP mice.

CONCLUSION

Nrf2 pathway protects bladder injury and ameliorates bladder dysfunction in IC, possibly by upregulating antioxidant genes and inhibiting oxidative stress.

Для цитирования: Ni Bin, Chen Zhengsen, Shu Le, Shao Yunpeng, Huang Yi, Tamrat Nebiyu Elias, Wei Zhongqing, Shen Baixin. Nrf2 Pathway Ameliorates Bladder Dysfunction in Cyclophosphamide-Induced Cystitis via Suppression of Oxidative Stress.. Oxidative medicine and cellular longevity. 2021. DOI: 10.1155/2021/4009308.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.