• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

雌雄老鼠的进食结构。

The feeding microstructure of male and female mice.

机构信息

Department of Pharmacology and Toxicology, School of Medicine, Wright State University, Dayton, OH, United States of America.

出版信息

PLoS One. 2021 Feb 4;16(2):e0246569. doi: 10.1371/journal.pone.0246569. eCollection 2021.

DOI:10.1371/journal.pone.0246569
PMID:33539467
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7861458/
Abstract

The feeding pattern and control of energy intake in mice housed in groups are poorly understood. Here, we determined and quantified the normal feeding microstructure of social male and female mice of the C57BL/6J genetic background fed a chow diet. Mice at 10w, 20w and 30w of age showed the expected increase in lean and fat mass, being the latter more pronounced and variable in males than in females. Under ad libitum conditions, 20w and 30w old females housed in groups showed significantly increased daily energy intake when adjusted to body weight relative to age-matched males. This was the combined result of small increases in energy intake during the nocturnal and diurnal photoperiods of the day without major changes in the circadian pattern of energy intake or spontaneous ambulatory activity. The analysis of the feeding microstructure suggests sex- and age-related contributions of meal size, meal frequency and intermeal interval to the control of energy intake under stable energy balance, but not under negative energy balance imposed by prolonged fasting. During the night, 10-20w old females ate less frequently bigger meals and spent more time eating them resulting in reduced net energy intake relative to age-matched males. In addition, male and female mice at all ages tested significantly shortened the intermeal interval during the first hours of re-feeding in response to fasting without affecting meal size. Further, 20-30w old males lengthened their intermeal interval as re-feeding time increased to reach fed-levels faster than age-matched females. Collectively, our results suggest that the physiological mechanisms controlling meal size (satiation) and the non-eating time spent between meals (satiety) during stable or negative energy balance are regulated in a sex- and age-dependent manner in social mice.

摘要

群体饲养的小鼠的进食模式和能量摄入控制了解甚少。在这里,我们确定并量化了 C57BL/6J 遗传背景下社交雄性和雌性小鼠的正常进食微观结构,这些小鼠喂食标准饮食。10 周、20 周和 30 周龄的小鼠表现出瘦体重和脂肪量的预期增加,后者在雄性中比在雌性中更为明显和多变。在自由进食条件下,与年龄匹配的雄性相比,20 周和 30 周龄的群居雌性小鼠的每日能量摄入量相对体重显著增加。这是由于白天的夜间和白天光周期内能量摄入略有增加,而能量摄入的昼夜节律或自发活动没有发生重大变化所致。进食微观结构的分析表明,在稳定的能量平衡下,性别和年龄相关的餐量、进餐频率和两餐之间的间隔对能量摄入的控制有贡献,但在延长禁食引起的负能量平衡下则没有。在夜间,10-20 周龄的雌性小鼠进食频率较低,餐量较大,进食时间较长,导致与年龄匹配的雄性相比净能量摄入减少。此外,所有测试年龄的雄性和雌性小鼠在禁食后,为响应重新进食,显著缩短了两餐之间的间隔,而不影响餐量。此外,20-30 周龄的雄性小鼠随着重新进食时间的增加而延长两餐之间的间隔,以比年龄匹配的雌性更快地达到进食水平。总之,我们的研究结果表明,在稳定或负能量平衡下控制餐量(饱腹感)和两餐之间非进食时间(满足感)的生理机制在社交小鼠中以性别和年龄依赖的方式进行调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/c9d402a9d856/pone.0246569.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/194eafd13034/pone.0246569.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/9fbfb1bfe530/pone.0246569.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/62f550b1212b/pone.0246569.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/8f681374110c/pone.0246569.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/ee5a1f07cc34/pone.0246569.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/941aa739d3f7/pone.0246569.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/e4a3caada1e1/pone.0246569.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/c9d402a9d856/pone.0246569.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/194eafd13034/pone.0246569.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/9fbfb1bfe530/pone.0246569.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/62f550b1212b/pone.0246569.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/8f681374110c/pone.0246569.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/ee5a1f07cc34/pone.0246569.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/941aa739d3f7/pone.0246569.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/e4a3caada1e1/pone.0246569.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/847c/7861458/c9d402a9d856/pone.0246569.g008.jpg

相似文献

1
The feeding microstructure of male and female mice.雌雄老鼠的进食结构。
PLoS One. 2021 Feb 4;16(2):e0246569. doi: 10.1371/journal.pone.0246569. eCollection 2021.
2
Large, binge-type meals of high fat diet change feeding behaviour and entrain food anticipatory activity in mice.高脂肪饮食的大量暴饮暴食式进餐会改变小鼠的进食行为并引发食物预期活动。
Appetite. 2014 Jun;77(100):60-71. doi: 10.1016/j.appet.2014.02.020. Epub 2014 Mar 12.
3
Time-dependent changes in feeding behavior and energy balance associated with weight gain in mice fed obesogenic diets.摄食行为和能量平衡随摄食致肥胖饮食诱导的体重增加的时相变化。
Obesity (Silver Spring). 2024 Jul;32(7):1373-1388. doi: 10.1002/oby.24052.
4
Impact of physical activity level and dietary fat content on passive overconsumption of energy in non-obese adults.身体活动水平和膳食脂肪含量对非肥胖成年人被动能量过度摄入的影响。
Int J Behav Nutr Phys Act. 2017 Feb 6;14(1):14. doi: 10.1186/s12966-017-0473-3.
5
loss in insulin-secreting β-cells links development of overweight and metabolic dysregulation to impaired satiation control of feeding.胰岛素分泌β细胞的损失将超重和代谢失调的发展与进食饱食控制受损联系起来。
Am J Physiol Endocrinol Metab. 2023 Nov 1;325(5):E581-E594. doi: 10.1152/ajpendo.00197.2023. Epub 2023 Oct 11.
6
Meal pattern alterations associated with intermittent fasting for weight loss are normalized after high-fat diet re-feeding.与间歇性禁食以减轻体重相关的饮食模式改变在重新喂食高脂饮食后恢复正常。
Physiol Behav. 2017 May 15;174:49-56. doi: 10.1016/j.physbeh.2017.02.046. Epub 2017 Mar 3.
7
Fat intake and energy-balance effects.脂肪摄入与能量平衡效应。
Physiol Behav. 2004 Dec 30;83(4):579-85. doi: 10.1016/j.physbeh.2004.07.027.
8
Decreased thermic effect of food after an irregular compared with a regular meal pattern in healthy lean women.与规律进餐模式相比,健康瘦女性不规律进餐后食物的热效应降低。
Int J Obes Relat Metab Disord. 2004 May;28(5):653-60. doi: 10.1038/sj.ijo.0802616.
9
Ghrelin receptor regulates appetite and satiety during aging in mice by regulating meal frequency and portion size but not total food intake.胃饥饿素受体通过调节进食频率和食量而非总食物摄入量来调控小鼠衰老过程中的食欲和饱腹感。
J Nutr. 2014 Sep;144(9):1349-55. doi: 10.3945/jn.114.191171. Epub 2014 Jul 2.
10
Caloric intake and eating behavior in infants and toddlers with cystic fibrosis.患有囊性纤维化的婴幼儿的热量摄入与饮食行为
Pediatrics. 2002 May;109(5):E75-5. doi: 10.1542/peds.109.5.e75.

引用本文的文献

1
Obesogenic effects of warm temperature involve feeding adaptation by preoptic area leptin receptor neurons.温暖温度的致肥胖效应涉及视前区瘦素受体神经元对进食的适应性调节。
Res Sq. 2025 Aug 21:rs.3.rs-7032725. doi: 10.21203/rs.3.rs-7032725/v1.
2
Sex differences in visually guided orienting behavior emerges during adolescence in mice.视觉引导的定向行为中的性别差异在小鼠青春期出现。
iScience. 2025 Jul 22;28(8):113145. doi: 10.1016/j.isci.2025.113145. eCollection 2025 Aug 15.
3
The effect of amycretin, a unimolecular glucagon-like peptide-1 and amylin receptor agonist, on body weight and metabolic dysfunction in mice and rats.

本文引用的文献

1
The epidemiology of fighting in group-housed laboratory mice.群居饲养实验鼠的争斗行为的流行病学研究。
Sci Rep. 2020 Oct 6;10(1):16649. doi: 10.1038/s41598-020-73620-0.
2
Individual housing of male C57BL/6J mice after weaning impairs growth and predisposes for obesity.断奶后对雄性C57BL/6J小鼠进行单独饲养会损害其生长并使其易患肥胖症。
PLoS One. 2020 May 26;15(5):e0225488. doi: 10.1371/journal.pone.0225488. eCollection 2020.
3
A big-data approach to understanding metabolic rate and response to obesity in laboratory mice.大数据方法在实验室小鼠代谢率和肥胖反应研究中的应用。
胰淀素(一种单分子胰高血糖素样肽-1和胰淀素受体激动剂)对小鼠和大鼠体重及代谢功能障碍的影响。
EBioMedicine. 2025 Jul 23;118:105862. doi: 10.1016/j.ebiom.2025.105862.
4
Stratification of the Extent of Visual Impairment Identifies Sex-Specific Degenerative Changes in Retinal Structure and Function during Aging.视力损害程度分层可识别衰老过程中视网膜结构和功能的性别特异性退行性变化。
J Integr Neurosci. 2025 Mar 4;24(3):25805. doi: 10.31083/JIN25805.
5
Intranasal Delivery of a Ghrelin Mimetic Engages the Brain Ghrelin Signaling System in Mice.胃饥饿素模拟物经鼻给药激活小鼠大脑中的胃饥饿素信号系统。
Endocrinology. 2025 Feb 5;166(3). doi: 10.1210/endocr/bqae166.
6
Neuronal lipid droplets play a conserved and sex-biased role in maintaining whole-body energy homeostasis.神经元脂滴在维持全身能量稳态中发挥着保守且具有性别偏向性的作用。
bioRxiv. 2024 Sep 20:2024.09.19.613929. doi: 10.1101/2024.09.19.613929.
7
A Light-Responsive Neural Circuit Suppresses Feeding.光响应性神经回路抑制摄食。
J Neurosci. 2024 Jul 24;44(30):e2192232024. doi: 10.1523/JNEUROSCI.2192-23.2024.
8
Longitudinal monitoring of the mouse brain reveals heterogenous network trajectories during aging.纵向监测小鼠大脑在衰老过程中揭示了不同的网络轨迹。
Commun Biol. 2024 Feb 20;7(1):210. doi: 10.1038/s42003-024-05873-8.
9
loss in insulin-secreting β-cells links development of overweight and metabolic dysregulation to impaired satiation control of feeding.胰岛素分泌β细胞的损失将超重和代谢失调的发展与进食饱食控制受损联系起来。
Am J Physiol Endocrinol Metab. 2023 Nov 1;325(5):E581-E594. doi: 10.1152/ajpendo.00197.2023. Epub 2023 Oct 11.
10
Delayed skeletal development and IGF-1 deficiency in a mouse model of lysinuric protein intolerance.赖氨酸尿蛋白不耐受症小鼠模型中的骨骼发育迟缓及 IGF-1 缺乏
Dis Model Mech. 2023 Aug 1;16(8). doi: 10.1242/dmm.050118. Epub 2023 Aug 17.
Elife. 2020 May 1;9:e53560. doi: 10.7554/eLife.53560.
4
Gonadal hormones influence core body temperature during calorie restriction.在热量限制期间,性腺激素会影响核心体温。
Temperature (Austin). 2019 Apr 26;6(2):158-168. doi: 10.1080/23328940.2019.1607653. eCollection 2019.
5
Towards large scale automated cage monitoring - Diurnal rhythm and impact of interventions on in-cage activity of C57BL/6J mice recorded 24/7 with a non-disrupting capacitive-based technique.迈向大规模自动化笼内监测 - 使用非干扰电容式技术 24/7 记录 C57BL/6J 小鼠笼内活动的昼夜节律和干预措施的影响。
PLoS One. 2019 Feb 4;14(2):e0211063. doi: 10.1371/journal.pone.0211063. eCollection 2019.
6
Home alone: a systematic review and meta-analysis on the effects of individual housing on body weight, food intake and visceral fat mass in rodents.独居:个体住房对啮齿动物体重、食物摄入量和内脏脂肪量影响的系统评价和荟萃分析。
Obes Rev. 2018 May;19(5):614-637. doi: 10.1111/obr.12663. Epub 2018 Jan 15.
7
Time-course and dynamics of obesity-related behavioral changes induced by energy-dense foods in mice.高脂肪食物诱导小鼠肥胖相关行为变化的时程和动态。
Addict Biol. 2018 Mar;23(2):531-543. doi: 10.1111/adb.12595. Epub 2018 Jan 10.
8
To Group or Not to Group? Good Practice for Housing Male Laboratory Mice.分组还是不分组?雄性实验小鼠饲养的良好做法。
Animals (Basel). 2017 Nov 24;7(12):88. doi: 10.3390/ani7120088.
9
Estradiol and the control of feeding behavior.雌二醇与摄食行为的调控
Steroids. 2018 May;133:44-52. doi: 10.1016/j.steroids.2017.11.011. Epub 2017 Nov 24.
10
Psychological stress exposure to aged mice causes abnormal feeding patterns with changes in the bout number.对老年小鼠施加心理压力会导致进食模式异常,且进食次数发生改变。
Aging (Albany NY). 2017 Nov 9;9(11):2269-2287. doi: 10.18632/aging.101320.