Verapamil inhibits 3T3-L1 preadipocyte differentiation

Nan Gu , Shi Liu , Xirong Guo , Li Fei , Xiaoqin Pan , Mei Guo , Ronghua Chen
{"title":"Verapamil inhibits 3T3-L1 preadipocyte differentiation","authors":"Nan Gu ,&nbsp;Shi Liu ,&nbsp;Xirong Guo ,&nbsp;Li Fei ,&nbsp;Xiaoqin Pan ,&nbsp;Mei Guo ,&nbsp;Ronghua Chen","doi":"10.1016/S1007-4376(09)60090-3","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To investigate the effect of the calcium channel blocker verapamil on adipocyte differentiation and its mechanism of action.</p></div><div><h3>Methods</h3><p>Preadipocytes from 3T3-L1 strain mouse embryos were cultured and differentiated into matured adipocytes <em>in vitro</em>. Verapamil was added to the culture medium in the concentration of 30 μmol/L on Day 0. Cell differentiation was determined by Oil Red O staining and marker gene mRNA expression was evaluated and compared by RT-PCR. The fluo-3/AM probe and laser scanning confocal microscopy were used to measure intracellular calcium concentrations.</p></div><div><h3>Results</h3><p><figure><img></figure> The differentiation rate of 3T3-L1 preadipocytes exposed to verapamil was lower than that of untreated cells. <figure><img></figure>Verapamil promoted the retention of pref-1 gene expression. Lipoprotein lipase expression in the verapamil group was significantly lower than that in the control group on Day 4, Day 6 and Day 8 (<em>P</em> &lt; 0.05) and resistin expression was significantly lower than that in the control group on Day 6, Day 8 and Day 10 (<em>P</em> &lt; 0.05). Fatty acid synthase expression in the verapamil group was significantly lower than that in the control group from Day 2 (<em>P</em> &lt; 0.05). <figure><img></figure> Intracellular concentrations of calcium [Ca<sup>2+</sup>]i in the verapamil group were significantly decreased compared with those in the control group on Day 2, Day 4 and Day 6 (<em>P</em> &lt; 0.05), while there was no obvious difference between the two groups on Day 0 (<em>P</em> &gt; 0.05).</p></div><div><h3>Conclusion</h3><p>In 3T3-L1 preadipocytes verapamil significantly reduced adipocyte differentiation, down-regulated the mRNA expression of three marker genes for adipocytes differentiation, and prolonged the mRNA expression of an inhibitor of differentiation. The inhibitory effect of verapamil on differentiation may involve its role as a blocker of calcium influx in adipocytes.</p></div>","PeriodicalId":100807,"journal":{"name":"Journal of Nanjing Medical University","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2009-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1007-4376(09)60090-3","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nanjing Medical University","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1007437609600903","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Objective

To investigate the effect of the calcium channel blocker verapamil on adipocyte differentiation and its mechanism of action.

Methods

Preadipocytes from 3T3-L1 strain mouse embryos were cultured and differentiated into matured adipocytes in vitro. Verapamil was added to the culture medium in the concentration of 30 μmol/L on Day 0. Cell differentiation was determined by Oil Red O staining and marker gene mRNA expression was evaluated and compared by RT-PCR. The fluo-3/AM probe and laser scanning confocal microscopy were used to measure intracellular calcium concentrations.

Results

The differentiation rate of 3T3-L1 preadipocytes exposed to verapamil was lower than that of untreated cells.
Verapamil promoted the retention of pref-1 gene expression. Lipoprotein lipase expression in the verapamil group was significantly lower than that in the control group on Day 4, Day 6 and Day 8 (P < 0.05) and resistin expression was significantly lower than that in the control group on Day 6, Day 8 and Day 10 (P < 0.05). Fatty acid synthase expression in the verapamil group was significantly lower than that in the control group from Day 2 (P < 0.05).
Intracellular concentrations of calcium [Ca2+]i in the verapamil group were significantly decreased compared with those in the control group on Day 2, Day 4 and Day 6 (P < 0.05), while there was no obvious difference between the two groups on Day 0 (P > 0.05).

Conclusion

In 3T3-L1 preadipocytes verapamil significantly reduced adipocyte differentiation, down-regulated the mRNA expression of three marker genes for adipocytes differentiation, and prolonged the mRNA expression of an inhibitor of differentiation. The inhibitory effect of verapamil on differentiation may involve its role as a blocker of calcium influx in adipocytes.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
维拉帕米抑制3T3-L1前脂肪细胞分化
目的探讨钙通道阻滞剂维拉帕米对脂肪细胞分化的影响及其作用机制。方法体外培养3T3-L1系小鼠胚胎脂肪细胞,并将其分化为成熟脂肪细胞。第0天在培养基中加入维拉帕米,浓度为30 μmol/L。油红O染色检测细胞分化情况,RT-PCR检测标记基因mRNA表达水平。使用fluo-3/AM探针和激光扫描共聚焦显微镜测量细胞内钙浓度。结果维拉帕米处理的3T3-L1前脂肪细胞分化率低于未处理的细胞。维拉帕米促进pref-1基因表达的保留。维拉帕米组在第4天、第6天、第8天的脂蛋白脂肪酶表达量显著低于对照组(P <在第6天、第8天和第10天,抵抗素的表达显著低于对照组(P <0.05)。维拉帕米组脂肪酸合成酶的表达从第2天起显著低于对照组(P <0.05)。维拉帕米组细胞内钙[Ca2+]i浓度在第2天、第4天和第6天与对照组相比显著降低(P <0.05),而第0天两组间差异无统计学意义(P >0.05)。结论维拉帕米可显著抑制3T3-L1前脂肪细胞的分化,下调3个脂肪细胞分化标志基因的mRNA表达,延长1个分化抑制基因的mRNA表达。维拉帕米对分化的抑制作用可能涉及其作为脂肪细胞钙内流的阻滞剂的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Effects of sevoflurane on left ventricular function by speckle-tracking echocardiography in coronary bypass patients: A randomized trial Phosphorylated protein chip combined with artificial intelligence tools for precise drug screening Upregulation of α-ENaC induces pancreatic β-cell dysfunction, ER stress, and SIRT2 degradation Irisin/BDNF signaling in the muscle-brain axis and circadian system: a review ELABELA protects against diabetic kidney disease by activating high glucose-inhibited renal tubular autophagy
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1