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Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats
Store operated calcium channels (SOCCs) have been suggested to play a critical role in many diabetic complications. Diabetic cystopathy (DCP) is common in patients with diabetes, but the role of SOCCs in DCP is still unclear. The aim of the present study was to investigate the role of SOCCs in DCP w...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928646/ https://www.ncbi.nlm.nih.gov/pubmed/29532875 http://dx.doi.org/10.3892/mmr.2018.8723 |
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author | Yang, Sen Wang, Dongwen Cao, Xiaoming Zhang, Xuhui Yuan, Xiaobin Yang, Tiancheng Mi, Yang |
author_facet | Yang, Sen Wang, Dongwen Cao, Xiaoming Zhang, Xuhui Yuan, Xiaobin Yang, Tiancheng Mi, Yang |
author_sort | Yang, Sen |
collection | PubMed |
description | Store operated calcium channels (SOCCs) have been suggested to play a critical role in many diabetic complications. Diabetic cystopathy (DCP) is common in patients with diabetes, but the role of SOCCs in DCP is still unclear. The aim of the present study was to investigate the role of SOCCs in DCP with streptozocin (STZ)-induced diabetic rats. Specifically, the authors investigated whether SOCCs were altered in streptozocin (STZ)-induced diabetic rats and, if so, how this may contribute to the contraction of bladder detrusor strips and the intracellular Ca(2+) concentration of bladder smooth muscle cells in diabetic rats. Cyclopiazonic acid (CPA, 10 µM) and SKF-96365 (10 µM) were used to activate and inhibit SOCCs respectively, to research the effects of SOCCs on the contraction of the bladder detrusor strips in normal and STZ-induced diabetic rats at the 4th, 8th and 12th week after the diabetic rat model was established. The changes of intracellular Ca(2+) were also evaluated under confocal microscopy with pretreated Fluo-4AM. In addition, the expressions of Orai1 and STIM1 were detected by reverse transcription-quantitative polymerase chain reaction and western blotting at different time points. According to the results, the contractive frequency of diabetic bladder muscle strips was higher than that of controls in the 4th and 8th week. The increased fluorescence intensity was detected after using CPA and SKF-96365 in diabetic groups. The expressions of Orai1 and STIM1 changed in a time-dependent manner. |
format | Online Article Text |
id | pubmed-5928646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-59286462018-05-07 Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats Yang, Sen Wang, Dongwen Cao, Xiaoming Zhang, Xuhui Yuan, Xiaobin Yang, Tiancheng Mi, Yang Mol Med Rep Articles Store operated calcium channels (SOCCs) have been suggested to play a critical role in many diabetic complications. Diabetic cystopathy (DCP) is common in patients with diabetes, but the role of SOCCs in DCP is still unclear. The aim of the present study was to investigate the role of SOCCs in DCP with streptozocin (STZ)-induced diabetic rats. Specifically, the authors investigated whether SOCCs were altered in streptozocin (STZ)-induced diabetic rats and, if so, how this may contribute to the contraction of bladder detrusor strips and the intracellular Ca(2+) concentration of bladder smooth muscle cells in diabetic rats. Cyclopiazonic acid (CPA, 10 µM) and SKF-96365 (10 µM) were used to activate and inhibit SOCCs respectively, to research the effects of SOCCs on the contraction of the bladder detrusor strips in normal and STZ-induced diabetic rats at the 4th, 8th and 12th week after the diabetic rat model was established. The changes of intracellular Ca(2+) were also evaluated under confocal microscopy with pretreated Fluo-4AM. In addition, the expressions of Orai1 and STIM1 were detected by reverse transcription-quantitative polymerase chain reaction and western blotting at different time points. According to the results, the contractive frequency of diabetic bladder muscle strips was higher than that of controls in the 4th and 8th week. The increased fluorescence intensity was detected after using CPA and SKF-96365 in diabetic groups. The expressions of Orai1 and STIM1 changed in a time-dependent manner. D.A. Spandidos 2018-05 2018-03-09 /pmc/articles/PMC5928646/ /pubmed/29532875 http://dx.doi.org/10.3892/mmr.2018.8723 Text en Copyright: © Yang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Yang, Sen Wang, Dongwen Cao, Xiaoming Zhang, Xuhui Yuan, Xiaobin Yang, Tiancheng Mi, Yang Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats |
title | Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats |
title_full | Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats |
title_fullStr | Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats |
title_full_unstemmed | Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats |
title_short | Store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats |
title_sort | store operated calcium channels are associated with diabetic cystopathy in streptozotocin-induced diabetic rats |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5928646/ https://www.ncbi.nlm.nih.gov/pubmed/29532875 http://dx.doi.org/10.3892/mmr.2018.8723 |
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