Suppr超能文献

肥胖易感和肥胖抵抗大鼠舌头上 CD36 减少,导致其对亚油酸的偏好减弱。

Preference for linoleic acid in obesity-prone and obesity-resistant rats is attenuated by the reduction of CD36 on the tongue.

机构信息

Joint Diabetes, Endocrinology and Metabolism Program, Louisiana State University System, Louisiana State University Health Science Center-New Orleans, New Orleans, Lousiana; and.

出版信息

Am J Physiol Regul Integr Comp Physiol. 2013 Dec;305(11):R1346-55. doi: 10.1152/ajpregu.00582.2012. Epub 2013 Oct 23.

Abstract

Differential sensing of dietary fat and fatty acids by the oral cavity is proposed to regulate the susceptibility to obesity. In the current experiments, animals that differ in their susceptibility to obesity were used to investigate the influence of the oral cavity on the preference for the polyunsaturated fatty acid, linoleic acid. In experiment 1, the preference for differing concentrations of linoleic acid was determined in obesity-prone Osborne-Mendel (OM) and obesity-resistant S5B/Pl (S5B) rats. The preference threshold for linoleic acid was lower in S5B rats, compared with OM rats. To determine whether differences in linoleic acid preference threshold were related to innate strain differences in the fatty acid receptors on the tongue, the expression of GPR120, GPR40, and CD36 on the circumvallate papillae were assessed in OM and S5B rats. Results indicated that the expression of CD36, GPR40, and GPR120 did not differ between these two strains. Numerous studies have examined the role of CD36 on fat intake; therefore, in experiment 3, RNA interference was used to decrease the expression of CD36 on the tongues of OM and S5B rats, and the effect of decreased CD36 expression on linoleic acid preference was determined. CD36 siRNA attenuated linoleic acid preference for the most preferred concentration in both OM and S5B rats. Overall, these data indicate that there are innate differences in the preference threshold for linoleic acid in obesity-prone and obesity-resistant rats. Experimentally reducing the expression of CD36 on the circumvallate papillae attenuated the preference for linoleic acid in both strains.

摘要

口腔对膳食脂肪和脂肪酸的差异感知被认为可以调节肥胖的易感性。在目前的实验中,使用肥胖易感性不同的动物来研究口腔对多不饱和脂肪酸亚油酸的偏好的影响。在实验 1 中,确定了肥胖易感的奥斯本-门德尔(OM)和肥胖抗性 S5B/Pl(S5B)大鼠对不同浓度亚油酸的偏好。与 OM 大鼠相比,S5B 大鼠对亚油酸的偏好阈值较低。为了确定亚油酸偏好阈值的差异是否与舌上脂肪酸受体的先天品系差异有关,评估了 OM 和 S5B 大鼠的味状乳头 GPR120、GPR40 和 CD36 的表达。结果表明,这两种品系之间 CD36、GPR40 和 GPR120 的表达没有差异。许多研究已经研究了 CD36 在脂肪摄入中的作用;因此,在实验 3 中,使用 RNA 干扰降低 OM 和 S5B 大鼠舌上 CD36 的表达,并确定 CD36 表达降低对亚油酸偏好的影响。CD36 siRNA 减弱了 OM 和 S5B 大鼠对最偏好浓度亚油酸的偏好。总的来说,这些数据表明肥胖易感和肥胖抗性大鼠对亚油酸的偏好阈值存在先天差异。实验性地降低味状乳头上 CD36 的表达减弱了两种品系对亚油酸的偏好。

相似文献

1
Preference for linoleic acid in obesity-prone and obesity-resistant rats is attenuated by the reduction of CD36 on the tongue.
Am J Physiol Regul Integr Comp Physiol. 2013 Dec;305(11):R1346-55. doi: 10.1152/ajpregu.00582.2012. Epub 2013 Oct 23.
2
Lingual CD36 and nutritional status differentially regulate fat preference in obesity-prone and obesity-resistant rats.
Physiol Behav. 2017 May 15;174:120-127. doi: 10.1016/j.physbeh.2017.03.015. Epub 2017 Mar 14.
7
Fatty acid responses in taste cells from obesity-prone and -resistant rats.
Physiol Behav. 2005 Dec 15;86(5):681-90. doi: 10.1016/j.physbeh.2005.08.057. Epub 2005 Oct 24.
9
High-fat diet differentially regulates metabolic parameters in obesity-resistant S5B/Pl rats and obesity-prone Osborne-Mendel rats.
Can J Physiol Pharmacol. 2016 Feb;94(2):206-215. doi: 10.1139/cjpp-2015-0141. Epub 2015 Aug 14.
10
Effect of a beta-3 agonist on food intake in two strains of rats that differ in susceptibility to obesity.
Physiol Behav. 2004 Sep 15;82(2-3):489-96. doi: 10.1016/j.physbeh.2004.04.059.

引用本文的文献

1
Adiponectin Signaling Modulates Fat Taste Responsiveness in Mice.
Nutrients. 2024 Oct 30;16(21):3704. doi: 10.3390/nu16213704.
2
Orlistat mouth rinse: Using the tongue to deliver antiobesity medication in a double-blind randomized crossover pilot trial.
Diabetes Obes Metab. 2023 Aug;25(8):2236-2242. doi: 10.1111/dom.15101. Epub 2023 May 3.
3
The effect of maternal period nutritional status on oro-sensorial fat perception and taste preference in rats.
Mol Cell Biochem. 2023 Dec;478(12):2861-2873. doi: 10.1007/s11010-023-04703-5. Epub 2023 Mar 21.
4
Huoxue Jiangtang Decoction Alleviates Type 2 Diabetes Mellitus by Regulating the Oral Microbiota and Food Preferences.
Diabetes Metab Syndr Obes. 2022 Nov 30;15:3739-3751. doi: 10.2147/DMSO.S391226. eCollection 2022.
6
Increased Fat Taste Preference in Progranulin-Deficient Mice.
Nutrients. 2021 Nov 17;13(11):4125. doi: 10.3390/nu13114125.
8
Cellular and Molecular Mechanisms of Fat Taste Perception.
Handb Exp Pharmacol. 2022;275:247-270. doi: 10.1007/164_2021_437.
10
Expression of neural markers of gustatory signaling are differentially altered by continuous and intermittent feeding patterns.
Physiol Behav. 2019 Dec 1;212:112719. doi: 10.1016/j.physbeh.2019.112719. Epub 2019 Oct 18.

本文引用的文献

4
STIM1 regulates calcium signaling in taste bud cells and preference for fat in mice.
J Clin Invest. 2012 Jun;122(6):2267-82. doi: 10.1172/JCI59953. Epub 2012 May 1.
7
CD36 and taste of fat.
Curr Opin Clin Nutr Metab Care. 2012 Mar;15(2):107-11. doi: 10.1097/MCO.0b013e32834ff19c.
8
The fatty acid translocase gene CD36 and lingual lipase influence oral sensitivity to fat in obese subjects.
J Lipid Res. 2012 Mar;53(3):561-566. doi: 10.1194/jlr.M021873. Epub 2011 Dec 31.
10
Oral and gastrointestinal sensing of dietary fat and appetite regulation in humans: modification by diet and obesity.
Front Neurosci. 2010 Oct 19;4:178. doi: 10.3389/fnins.2010.00178. eCollection 2010.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验