Nuclear receptors such as pregnane X receptor (PXR) and constitutive androstane receptor (CAR) regulate the transcription of transporter and cytochrome P450 (CYP). The diurnal variation was observed in some transporters regulated by nuclear receptors. We investigated whether diurnal variation in PXR and CAR exists in mice. We also examined the effect of food intake on the diurnal rhythm of hepatic PXR and CAR using fed and fasted mice. In liver and small intestine of fed mice, the mRNA levels of PXR and CAR were unchanged between 7:00 AM and 7:00 PM. In contrast to fed mice, fasting mice partly exhibited the diurnal variation in PXR, not in CAR. The mRNA levels of PXR at 7:00 AM were significantly higher than that those at 7:00 PM in liver of fasting mice. These results indicated the different effects of fasting in mice on diurnal variation of PXR in each tissue.
The nuclear receptors pregnane X receptor (PXR, NR1I2: GenBank NM_010936) and constitutive androstane receptor (CAR, NR1I3: GenBank NM_009803) are involved in the primary response to xenobiotics and endogenous toxins. These receptors respond to ligands by activating the expressions of genes encoding enzymes involved in phase I (functionalization reactions) and phase II (conjugation reactions) metabolism and transporters [1-3]. Recent studies have shown that the gene expression of several transporters such as H+/peptide cotransporter PEPT1 [
In the present study, we investigated the diurnal variation of PXR and CAR in mice liver and small intestine. We also determined whether the fasting influences the diurnal variation of PXR and CAR. This information is important for the determination of alteration in transporters regulated by PXR and CAR.
Five to 6 weeks old male ddY mice were purchased from Japan SLC Co. (Shizuoka, Japan). Mice were housed in an air-conditioned room at 22˚C ± 0.5˚C with a 12-h lighting schedule (7:00 AM-7:00 PM) and were fed on the light/dark schedule for 1 week before they were divided into fed and fasted groups. Four different groups of mice were used in this study: 1) control group fed normal chow (MF, Oriental Yeast Co., Tokyo, Japan) sacrificed at 7:00 AM; 2) control group fed normal chow sacrificed at 7:00 PM; 3) fasted for 3 days sacrificed at 7:00 AM and 4) fasted for 3 days sacrificed at 7:00 PM. Water was available to all groups throughout the experiments. The experiments were approved by the Committee for the Care and Use of Laboratory Animals at Kinki University School of Pharmaceutical Science.
The liver and small intestine were removed from mice with/without fasting after anesthesia by inhalation of ether and euthanasia by cervical dislocation. The small intestine was flushed with 50 mL of ice-cold saline, and was excised. The small intestine was a length of about 5 cm removed from about 5 cm below the ligament of Treitz. Each sample was preserved at −80˚C until use after flash freezing with liquid nitrogen.
Total RNA was extracted from approximately 100 mg of each rat liver and small intestines using TRIzol Reagent (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s instructions. Following RNase-free DNase I treatment (TaKaRa, Shiga, Japan), approximately 500 ng total RNA, as evaluated by UV absorption at 260 nm, was reverse-transcribed to complementary DNA (cDNA) using a PrimeScript-RT reagent Kit (TaKaRa) according to the manufacturer’s instructions. The reactions were incubated for 15 min at 37˚C and 5 s at 85˚C. The reverse-transcribed cDNA was used as template for realtime polymerase chain reaction (PCR). Amplification was performed in 50-μL reaction mixtures containing 2 × SYBR Premix Ex Taq (TaKaRa), 0.2 μM primer set of target gene or ribosome 28S ribosomal RNA (28S rRNA) as endogenous reference. Amplification and detection were performed with an ABI PRISM 7000 (Applied Biosystems, Foster City, CA, USA). The PCR reactions were incubated at 95˚C for 10 s, and amplified by a 40 three-step cycles at 95˚C for 5 s, 55˚C for 20 s, and 72˚C for 31 s. The amount of 28S rRNA in each sample was also measured for normalization. For all PCR amplifications, we used the following oligonucleotide sequences designed by Primer Express 2.0 (Applied Biosystems): PXR: 5’-CCCATCAACGTAGAGGAGGA-3’ and 5’-GGGGGTTGGTAGTTCCAGAT-3’; CAR: 5’-GGAGGACCAGATCTCCCTTC-3’ and 5’-ATTTCATTGCCACTCCCAAG-3’; and 28S rRNA: 5’-CGGCTCTTCCTATCATTGTG-3’ and 5’-CCTGTCTCACGACGGTCTAA-3’. Data were analyzed using the ABI Prism 7000 SDS Software (Applied Biosystems) particularly for the multiplex comparative method. The relative quantitation of the amount of target mRNA in the tested tissue samples was accomplished by measuring Cycle thresholds (Ct). To determine the quantity of the target gene-specific transcripts present in the liver and small intestines, their respective Ct values were first normalized by subtracting the Ct value obtained from the ribosome 28S rRNA control (ΔCt = Ct, target – Ct, control). The concentration of gene-specific mRNA in the liver and small intestines of PM relative to each tissue of AM mouse was calculated by subtracting the normalized Ct values obtained for each tissue of AM mouse from those obtained from each tissue of PM mouse (ΔΔCt = ΔCt, PM – ΔCt, AM) and the relative concentration was determined (2−∆∆Ct).
Significant differences between mean values of the gene expression levels were estimated using Student’s unpaired t-test.