在喂食标准或肥胖促进饮食的大鼠中,Bimatoprost促进饱腹感并减轻体重增加。

Clayton Spada , Chau Vu , Iona Raymond , Warren Tong , Chia-Lin Chuang , Christopher Walker , Kerry Loomes , David F. Woodward , Neil J. Poloso
{"title":"在喂食标准或肥胖促进饮食的大鼠中,Bimatoprost促进饱腹感并减轻体重增加。","authors":"Clayton Spada ,&nbsp;Chau Vu ,&nbsp;Iona Raymond ,&nbsp;Warren Tong ,&nbsp;Chia-Lin Chuang ,&nbsp;Christopher Walker ,&nbsp;Kerry Loomes ,&nbsp;David F. Woodward ,&nbsp;Neil J. Poloso","doi":"10.1016/j.plefa.2022.102511","DOIUrl":null,"url":null,"abstract":"<div><p>Bimatoprost is a synthetic prostamide F<sub>2α</sub> analog that down-regulates adipogenesis in vitro. This effect has been attributed to participation in a negative feedback loop that regulates anandamide-induced adipogenesis. A follow-on investigation has now been conducted into the broader metabolic effects of bimatoprost using rats under both normal state and obesity-inducing conditions. Chronic bimatoprost administration attenuated weight gain in a dose dependent-manner in rats fed either standard [max effect −7%] or obesity-promoting diets [max effect −23%] over a 9–10 week period. Consistent with these findings, bimatoprost promoted satiety as measured by decreased food intake [max effect, −7%], gastric emptying [max effect, −33–50%] and decreased circulating concentrations of the gut hormones, ghrelin and GLP-1 [max effect, −33–50%]. Additionally, subcutaneous, and visceral fat mass were distinctly affected by treatment [−30% diet independent]. Taken together, these results suggest that bimatoprost regulates energy homeostasis through promoting satiety and a decrease in food intake. These newly reported activities of bimatoprost reveal an additional method of metabolic disease intervention for potential therapeutic exploitation.</p></div>","PeriodicalId":94179,"journal":{"name":"Prostaglandins, leukotrienes, and essential fatty acids","volume":"187 ","pages":"Article 102511"},"PeriodicalIF":3.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S0952327822001211/pdfft?md5=d0abb812458fb17f5a4a0935bf8b6a3e&pid=1-s2.0-S0952327822001211-main.pdf","citationCount":"1","resultStr":"{\"title\":\"Bimatoprost promotes satiety and attenuates body weight gain in rats fed standard or obesity-promoting diets.\",\"authors\":\"Clayton Spada ,&nbsp;Chau Vu ,&nbsp;Iona Raymond ,&nbsp;Warren Tong ,&nbsp;Chia-Lin Chuang ,&nbsp;Christopher Walker ,&nbsp;Kerry Loomes ,&nbsp;David F. Woodward ,&nbsp;Neil J. Poloso\",\"doi\":\"10.1016/j.plefa.2022.102511\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Bimatoprost is a synthetic prostamide F<sub>2α</sub> analog that down-regulates adipogenesis in vitro. This effect has been attributed to participation in a negative feedback loop that regulates anandamide-induced adipogenesis. A follow-on investigation has now been conducted into the broader metabolic effects of bimatoprost using rats under both normal state and obesity-inducing conditions. Chronic bimatoprost administration attenuated weight gain in a dose dependent-manner in rats fed either standard [max effect −7%] or obesity-promoting diets [max effect −23%] over a 9–10 week period. Consistent with these findings, bimatoprost promoted satiety as measured by decreased food intake [max effect, −7%], gastric emptying [max effect, −33–50%] and decreased circulating concentrations of the gut hormones, ghrelin and GLP-1 [max effect, −33–50%]. Additionally, subcutaneous, and visceral fat mass were distinctly affected by treatment [−30% diet independent]. Taken together, these results suggest that bimatoprost regulates energy homeostasis through promoting satiety and a decrease in food intake. These newly reported activities of bimatoprost reveal an additional method of metabolic disease intervention for potential therapeutic exploitation.</p></div>\",\"PeriodicalId\":94179,\"journal\":{\"name\":\"Prostaglandins, leukotrienes, and essential fatty acids\",\"volume\":\"187 \",\"pages\":\"Article 102511\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2022-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S0952327822001211/pdfft?md5=d0abb812458fb17f5a4a0935bf8b6a3e&pid=1-s2.0-S0952327822001211-main.pdf\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Prostaglandins, leukotrienes, and essential fatty acids\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0952327822001211\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Prostaglandins, leukotrienes, and essential fatty acids","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0952327822001211","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

摘要

比马前列素是一种合成的前列腺素F2α类似物,在体外下调脂肪生成。这种效应归因于参与调节阿南达胺诱导的脂肪形成的负反馈回路。一项后续的研究现在已经在正常状态和肥胖诱导条件下对比马前列素的更广泛的代谢作用进行了研究。在9-10周的时间内,给予慢性比马前列素以剂量依赖性的方式减轻了喂食标准[最大效应- 7%]或促进肥胖饮食[最大效应- 23%]的大鼠的体重增加。与这些发现一致,bimatoprost通过减少食物摄入量(最大效应,- 7%)、胃排空(最大效应,- 33-50%)和降低肠道激素、胃促生长素和GLP-1的循环浓度(最大效应,- 33-50%)来促进饱腹感。此外,皮下和内脏脂肪量明显受到治疗的影响[- 30%不依赖饮食]。综上所述,这些结果表明,bimatoprost通过促进饱腹感和减少食物摄入来调节能量稳态。这些新报道的比马前列素的活性揭示了代谢疾病干预的潜在治疗开发的另一种方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Bimatoprost promotes satiety and attenuates body weight gain in rats fed standard or obesity-promoting diets.

Bimatoprost is a synthetic prostamide F analog that down-regulates adipogenesis in vitro. This effect has been attributed to participation in a negative feedback loop that regulates anandamide-induced adipogenesis. A follow-on investigation has now been conducted into the broader metabolic effects of bimatoprost using rats under both normal state and obesity-inducing conditions. Chronic bimatoprost administration attenuated weight gain in a dose dependent-manner in rats fed either standard [max effect −7%] or obesity-promoting diets [max effect −23%] over a 9–10 week period. Consistent with these findings, bimatoprost promoted satiety as measured by decreased food intake [max effect, −7%], gastric emptying [max effect, −33–50%] and decreased circulating concentrations of the gut hormones, ghrelin and GLP-1 [max effect, −33–50%]. Additionally, subcutaneous, and visceral fat mass were distinctly affected by treatment [−30% diet independent]. Taken together, these results suggest that bimatoprost regulates energy homeostasis through promoting satiety and a decrease in food intake. These newly reported activities of bimatoprost reveal an additional method of metabolic disease intervention for potential therapeutic exploitation.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Prostaglandins, leukotrienes, and essential fatty acids
Prostaglandins, leukotrienes, and essential fatty acids Clinical Biochemistry, Endocrinology, Diabetes and Metabolism
CiteScore
5.30
自引率
0.00%
发文量
0
审稿时长
64 days
期刊最新文献
Gallein but not fluorescein enhances the PGD2-stimulated synthesis of osteoprotegerin and interleukin-6 in osteoblasts Omega-3 fatty acids mitigate skin damage caused by ultraviolet-B radiation The disparate effects of omega-3 PUFAs on intestinal microbial homeostasis in experimental rodents under physiological condition Resolvin D4 mitigates lipopolysaccharide-induced lung injury in mice Blood EPA and DHA status among people living in the United States from 2000 to 2023
×
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