Uptake and metabolism of mizoribine, an immunosuppressant, in L5178Y-R mouse lymphoma cells in vitro and peripheral blood mononuclear cells of rats and kidney transplant recipients in vivo

• Published in: Drug metabolism and pharmacokinetics 2018-10, Vol.33 (5), p.232-239
• Main Authors: Oda, Keisuke, Mori, Nobuhiro, Okumi, Masayoshi, Furusawa, Miyuki, Ishiguro, Masashi, Inoue, Kazuyuki, Shuto, Satoshi, Unagami, Kohei, Ishida, Hideki, Tanabe, Kazunari, Murakami, Teruo
• Format: Article
• Language: English
• Subjects: Adenosine - pharmacology; Administration, Oral; Animals; Immunosuppressive Agents - antagonists & inhibitors; Immunosuppressive Agents - metabolism; Kidney transplant patients; Kidney Transplantation; L5178Y-R mouse lymphoma cells; Leukemia L5178 - metabolism; Leukemia L5178 - pathology; Leukemia L5178 - therapy; Leukocytes, Mononuclear - drug effects; Leukocytes, Mononuclear - metabolism; Male; Mice; Mice, Inbred ICR; Mizoribine; Mizoribine-5′-monophosphate; mRNA expression of ENTs; Peripheral blood mononuclear cells (PBMCs); Rats; Rats, Sprague-Dawley; Ribonucleosides - antagonists & inhibitors; Ribonucleosides - metabolism
• ISSN: 1347-4367; 1880-0920
• DOI: 10.1016/j.dmpk.2018.08.007

The cellular uptake of mizoribine (MZR), an immunosuppressant, and metabolism of MZR to MZR-5′- monophosphate (MZRP), an active metabolite, were evaluated in L5178Y-R mouse lymphoma cells and peripheral blood mononuclear cells (PBMCs) of rats and kidney transplant recipients (KTRs, n = 22). Real-time PCR analysis revealed the expression of ENT1 and ENT2 mRNAs, but not of CNTs, in L5178Y-R cells and rat's PBMCs. In L5178Y-R cells, the uptake of MZR was suppressed by adenosine, a substrate for ENT1 and ENT2, but not by 5-(4-nitrobenzyl)-6-thioinosine (0.1 μM), an ENT1 inhibitor. Saturable metabolism of MZR to MZRP was observed. In rats, peak plasma concentrations of MZR and peak concentrations of MZR and MZRP in PBMCs were observed 3 h after oral administration. MZR disappeared from PBMCs in parallel with plasma MZR, but the disappearance of MZRP from PBMCs appeared to be slow. In KTRs, the mean plasma concentration of MZR 3–4 h after ingestion was 3.14 μg/ml and the mean MZRP concentration in PBMCs was 16.8% of MZR, reflecting the involvement of ENT in the uptake of MZR. A linear relationship was observed between plasma MZR concentrations ranging from 1 to 6 μg/ml and PBMC's MZRP concentrations ranging from 90 to 200 ng/ml. [Display omitted]