Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic.
Institute of Physiology, Czech Academy of Sciences, Prague, Czech Republic; Department of Physiology, Faculty of Science, Charles University, Prague, Czech Republic.
Comp Biochem Physiol C Toxicol Pharmacol. 2019 Dec;226:108607. doi: 10.1016/j.cbpc.2019.108607. Epub 2019 Aug 15.
The circadian clock system drives many physiological processes, including plasma concentration of glucocorticoids and epithelial transport of some ions and nutrients. As glucocorticoids entrain the circadian rhythms in various peripheral organs, we examined whether adrenalectomy affects the expression and circadian rhythmicity of intestinal transporters of the solute carrier (SLC) and ATP-binding cassette (ABC) families, which participate in intestinal barriers for absorption of nutrients, nonnutrients and oral drugs. The rat jejunum showed rhythmic circadian profiles of Sglt1, Pept1, Nhe3, Mdr1 and Mrp2 but not Mct1, Oct1, Octn1, Oatp1, Cnt1 and Bcrp. With the exception of Pept1 and Mct1, adrenalectomy decreased the expression of all rhythmic and arrhythmic transporters including the amplitude of Sglt1 and Nhe3 rhythms but minimally affected the phases of rhythmic transporters except of Nhe3. Similarly, adrenalectomy downregulated the expression of rhythmic (Pparα, Hlf, Pgc1α) and arrhythmic (Hnf1β, Hnf4α) transcription factors, which are known to regulate the expression of transporters. We conclude that endogenous corticosteroids have a profound effect on the expression of intestinal SLC and ABC transporters and their nuclear transcription factors. The circulating corticosteroids are necessary for maintaining upregulated expression of Sglt1, Oct1, Octn1, Oatp1, Cnt1, Nhe3, Mdr1, Bcrp, Mrp2, Pparα, Pgc1α, Hnf1β, Hnf4α and Hlf and for maintaining the high amplitude of Sglt1, Nhe3, Pparα, Pgc1α and Hlf circadian rhythms. The study demonstrates that signals from the adrenal gland are necessary for maintaining the expression of arrhythmic and rhythmic intestinal transporters and that changes in the secretion of corticosteroids associated with stress might reorganize intestinal transport barriers.
昼夜节律钟系统驱动许多生理过程,包括糖皮质激素的血浆浓度和一些离子和营养物质的上皮转运。由于糖皮质激素使各种外周器官的昼夜节律同步,我们研究了肾上腺切除术是否会影响肠道溶质载体 (SLC) 和 ATP 结合盒 (ABC) 家族转运体的表达和昼夜节律性,这些转运体参与肠道对营养物质、非营养物质和口服药物的吸收屏障。大鼠空肠显示 Sglt1、Pept1、Nhe3、Mdr1 和 Mrp2 的节律性昼夜节律特征,但 Mct1、Oct1、Octn1、Oatp1、Cnt1 和 Bcrp 则没有。除了 Pept1 和 Mct1 之外,肾上腺切除术降低了所有节律性和非节律性转运体的表达,包括 Sglt1 和 Nhe3 节律的振幅,但对除 Nhe3 之外的节律性转运体的相位影响最小。同样,肾上腺切除术下调了已知调节转运体表达的节律性(Pparα、Hlf、Pgc1α)和非节律性(Hnf1β、Hnf4α)转录因子的表达。我们得出结论,内源性皮质类固醇对肠道 SLC 和 ABC 转运体及其核转录因子的表达有深远影响。循环皮质类固醇对于维持 Sglt1、Oct1、Octn1、Oatp1、Cnt1、Nhe3、Mdr1、Bcrp、Mrp2、Pparα、Pgc1α、Hnf1β、Hnf4α 和 Hlf 的上调表达以及 Sglt1、Nhe3、Pparα、Pgc1α 和 Hlf 昼夜节律的高振幅是必要的。该研究表明,来自肾上腺的信号对于维持非节律性和节律性肠道转运体的表达是必要的,与应激相关的皮质类固醇分泌的变化可能会重新组织肠道转运屏障。