<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kono J</submitter><funding>NIDDK NIH HHS</funding><pagination>5037</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9102543</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(9)</volume><pubmed_abstract>Bladder inflammatory diseases cause various urinary symptoms, such as urinary frequency and painful urination, that impair quality of life. In this study, we used a mouse model of cyclophosphamide (CYP)-induced bladder inflammation and immortalized human urothelial (TRT-HU1) cells to explore the preventive potential of nobiletin (NOB), a polymethoxylated flavone enriched in citrus fruit peel, and investigate its mechanism of action in the bladder. Prophylaxis with PMF90 (60% NOB) attenuated the development of bladder inflammation and urinary symptoms in CYP-treated mice. PMF90 also reduced the upregulation of connexin 43 (Cx43), a major component of gap junction channels, in the bladder mucosa of CYP-treated mice. Stimulation of TRT-HU1 cells with the pro-inflammatory cytokine IL-1β increa</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Flavonoid Nobiletin Attenuates Cyclophosphamide-Induced Cystitis in Mice through Mechanisms That Involve Inhibition of IL-1β Induced Connexin 43 Upregulation and Gap Junction Communication in Urothelial Cells.</pubmed_title><pmcid>PMC9102543</pmcid><funding_grant_id>R01 DK122153</funding_grant_id><pubmed_authors>Ueda M</pubmed_authors><pubmed_authors>Negoro H</pubmed_authors><pubmed_authors>Kono J</pubmed_authors><pubmed_authors>Woo JT</pubmed_authors><pubmed_authors>Kobayashi T</pubmed_authors><pubmed_authors>Sengiku A</pubmed_authors><pubmed_authors>Suadicani SO</pubmed_authors><pubmed_authors>Ogawa O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Flavonoid Nobiletin Attenuates Cyclophosphamide-Induced Cystitis in Mice through Mechanisms That Involve Inhibition of IL-1β Induced Connexin 43 Upregulation and Gap Junction Communication in Urothelial Cells.</name><description>Bladder inflammatory diseases cause various urinary symptoms, such as urinary frequency and painful urination, that impair quality of life. In this study, we used a mouse model of cyclophosphamide (CYP)-induced bladder inflammation and immortalized human urothelial (TRT-HU1) cells to explore the preventive potential of nobiletin (NOB), a polymethoxylated flavone enriched in citrus fruit peel, and investigate its mechanism of action in the bladder. Prophylaxis with PMF90 (60% NOB) attenuated the development of bladder inflammation and urinary symptoms in CYP-treated mice. PMF90 also reduced the upregulation of connexin 43 (Cx43), a major component of gap junction channels, in the bladder mucosa of CYP-treated mice. Stimulation of TRT-HU1 cells with the pro-inflammatory cytokine IL-1β increa</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-18T15:03:20.975Z</modification><creation>2025-02-19T00:55:47.344Z</creation></dates><accession>S-EPMC9102543</accession><cross_references><pubmed>35563427</pubmed><doi>10.3390/ijms23095037</doi></cross_references></HashMap>