Department of Psychology, Brooklyn College, City University of New York, Brooklyn, New York, and.
Am J Physiol Regul Integr Comp Physiol. 2013 Dec 15;305(12):R1490-7. doi: 10.1152/ajpregu.00440.2013. Epub 2013 Oct 23.
In addition to orosensory signals, postoral actions of fat stimulate appetite and condition flavor preferences, but the gut sensors mediating these responses are unknown. Here, we investigated the role of the fatty acid sensors GPR40 and GPR120 in postoral and oral preferences for a soybean oil emulsion (Intralipid). Mice were trained to drink a flavored solution (CS+) paired with intragastric (IG) oil infusions and another flavored solution (CS-) paired with water infusions. Knockout (KO) mice missing GPR40 or GPR120 sensors increased their CS+ intake in one-bottle tests (1 h/day) but less so than wild-type (WT) mice. The KO mice also preferred the CS+ to CS- in a two-bottle test, but the preference was attenuated in GPR40 KO mice. Double-knockout (DoKO) mice missing both GPR40 and GPR120 displayed attenuated stimulation of CS+ intake and only a marginal CS+ preference. The DoKO mice developed a more substantial CS+ preference when tested 24 h/day, although weaker than that of WT mice. The DoKO mice also consumed less of the CS+ paired with IG Intralipid, as well as less Intralipid in oral tests. However, DoKO mice, like GPR40 KO and GPR120 KO mice did not differ from WT mice in their preference for Intralipid over water at 0.001%-20% concentrations. In contrast to prior results obtained with mice missing the CD36 fatty acid sensor, these findings indicate that, together, GPR40 and GPR120 play a critical role in the postoral stimulation of appetite by fat but are not essential for oral fat preferences.
除了口腔感觉信号外,脂肪的口腔后作用也会刺激食欲并调节味觉偏好,但介导这些反应的肠道传感器尚不清楚。在这里,我们研究了脂肪酸传感器 GPR40 和 GPR120 在口服脂肪后对大豆油乳液(Intralipid)的口腔后和口腔偏好中的作用。通过训练小鼠,使它们将一种带有甜味的溶液(CS+)与胃内(IG)油输注物配对,并将另一种带有甜味的溶液(CS-)与水输注物配对。缺失 GPR40 或 GPR120 传感器的 KO 小鼠在单瓶测试(每天 1 小时)中增加了对 CS+的摄入,但不如 WT 小鼠多。KO 小鼠在双瓶测试中也更喜欢 CS+而不是 CS-,但 GPR40 KO 小鼠的偏好程度降低。缺失 GPR40 和 GPR120 的双敲除(DoKO)小鼠对 CS+摄入的刺激作用减弱,仅表现出微弱的 CS+偏好。当对 DoKO 小鼠进行 24 小时测试时,它们表现出更强的 CS+偏好,但仍弱于 WT 小鼠。DoKO 小鼠还减少了与 IG Intralipid 配对的 CS+的摄入量,以及在口腔测试中减少了 Intralipid 的摄入量。然而,与缺失 CD36 脂肪酸传感器的小鼠的先前结果相反,这些发现表明,GPR40 和 GPR120 共同在脂肪的口腔后刺激食欲方面发挥关键作用,但对于口腔脂肪偏好并非必需。