There was an error in Figure 13 as published. The representative images related to Panel A have been inadvertently duplicated in Panel E. The corrected Figure 13 and its caption appear below. Effect of post-treatment (therapeutic administration) with RG100204 on the NF-ĸB signalling pathway and the activation NLRP3 inflammasome in the heart. Heart samples were collected at the end of the experiment and the NF-kB signalling pathway, as well as the activation of the NLRP3 inflammasome. Densitometry analysis of the bands is expressed as relative optical density (O.D.) of the (A) phosphorylation of IKKa/b at Ser178/180 corrected for the corresponding total IKKa/b content and normalized using the related sham band; (B) phosphorylation of IĸBa at Ser32/36 corrected for the corresponding total IĸBa content and normalized using the related sham band; (C) NF-ĸB p65 subunit levels in both, cytosolic and nuclear fractions expressed as a nucleus/cytosol ratio normalized using the related sham bands; (D) NLRP3 activation, corrected against tubulin and normalized using the related sham bands; and (E) proteolytic cleavage of pro-caspase-1 to activated caspase-1 and normalized using the related sham band. The following groups were studied: sham + vehicle (n = 5), CLP + vehicle (n = 10), CLP +RG100204 (1 h & 8 h) (n = 10). All data were analyzed by one-way ANOVA, followed by a Bonferroni’s post-hoc test. Data are expressed as mean ± SEM. **P < 0.01 and ****P < 0.0001 vs. the respective sham-operated group. The original article has been updated.
Correction: RG100204, a novel Aquaporin-9 inhibitor, reduces septic cardiomyopathy and multiple organ failure in murine sepsis
Gena, Patrizia;Tesse, Angela;Calamita, GiuseppeWriting – Review & Editing
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2025-01-01
Abstract
There was an error in Figure 13 as published. The representative images related to Panel A have been inadvertently duplicated in Panel E. The corrected Figure 13 and its caption appear below. Effect of post-treatment (therapeutic administration) with RG100204 on the NF-ĸB signalling pathway and the activation NLRP3 inflammasome in the heart. Heart samples were collected at the end of the experiment and the NF-kB signalling pathway, as well as the activation of the NLRP3 inflammasome. Densitometry analysis of the bands is expressed as relative optical density (O.D.) of the (A) phosphorylation of IKKa/b at Ser178/180 corrected for the corresponding total IKKa/b content and normalized using the related sham band; (B) phosphorylation of IĸBa at Ser32/36 corrected for the corresponding total IĸBa content and normalized using the related sham band; (C) NF-ĸB p65 subunit levels in both, cytosolic and nuclear fractions expressed as a nucleus/cytosol ratio normalized using the related sham bands; (D) NLRP3 activation, corrected against tubulin and normalized using the related sham bands; and (E) proteolytic cleavage of pro-caspase-1 to activated caspase-1 and normalized using the related sham band. The following groups were studied: sham + vehicle (n = 5), CLP + vehicle (n = 10), CLP +RG100204 (1 h & 8 h) (n = 10). All data were analyzed by one-way ANOVA, followed by a Bonferroni’s post-hoc test. Data are expressed as mean ± SEM. **P < 0.01 and ****P < 0.0001 vs. the respective sham-operated group. The original article has been updated.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


