Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Masako Nomiyama"'
Publikováno v:
Clinical and Experimental Nephrology. 2:117-123
Background We previously found that ticlopidine inhibits the proliferation of cultured rat mesangial cells that is induced by fetal bovine serum. This study was designed to examine the effects of ticlopidine on platelet-derived growth factor (PDGF)-i
Publikováno v:
Japanese Journal of Hospital Pharmacy. 24:17-22
The effect of two anti-platelet drugs, ticlopidine and dilazep, on the fetal bovine serum (FBS)-induced DNA synthesis of cultured rat renal mesangial cells was assessed by means of an [3H] thymidine incorporation assay. Each drug inhibited the 2% FBS
Autor:
Fumiaki Kitazawa, Kazuki Nagasawa, Teruyoshi Yokoyama, Noriaki Ohnishi, Masako Nomiyama, Toshiki Natazuka, Akiko Tsumura, Kazuo Chihara, Kohji Takara
Publikováno v:
Cancer Chemotherapy and Pharmacology. 37:297-304
We studied the transport mechanism of pirarubicin (THP) in HL60 and its THP-resistant (HL60/THP) cells, which showed no expression of mdr1 mRNA on Northern blot analysis. Under physiological conditions, the uptake of THP by both types of cell was tim
Publikováno v:
Biological and Pharmaceutical Bulletin. 19:100-105
We examined the transport mechanisms of daunorubicin (DNR) and doxorubicin (ADR) in HL60 and HL60/THP cells which were the non-P-glycoprotein-mediated resistant clone of the parent HL60 cells and showed a low degree of resistance, and compared them w
Publikováno v:
Biological and Pharmaceutical Bulletin. 19:1203-1209
We studied the transport mechanism of pirarubicin (THP) in mononuclear cells (MNCs) obtained from healthy human donors. The THP uptake was time-, temperature-, concentration- and energy (in part)-dependent. The uptake of daunorubicin (DNR) and doxoru
Publikováno v:
Biological and Pharmaceutical Bulletin. 19:971-976
We studied the uptake mechanisms of anthracycline derivatives, pirarubicin (THP), daunorubicin (DNR) and doxorubicin (ADR), in K562 and multidrug-resistant K562/ADM cells, which overexpress a multidrug efflux pump P-glycoprotein (P-gp). The uptake of
Autor:
Teruyoshi Yokoyama, Masako Nomiyama, Kazuki Nagasawa, Noriaki Ohnishi, Akiko Tsumura, Fumiaki Kitazawa
Publikováno v:
Biological and Pharmaceutical Bulletin. 18:368-371
We previously revealed that pirarubicin (THP) was actively taken up by rat polymorphonuclear leukocytes via a carrier-mediated transport system. In the experiment on the effects of the metabolic inhibitors, rotenone, 2,4-dinitrophenol and sodium cyan
Autor:
Katsuhiko Okumura, Seigo Iwakawa, Kazuki Nagasawa, Noriaki Ohnishi, Masako Nomiyama, Teruyoshi Yokoyama
Publikováno v:
Biological and Pharmaceutical Bulletin. 17:1305-1308
We performed experiments on the cis-inhibition and trans-stimulation effect on pirarubicin uptake in order to clarify the involvement of a carrier in the pirarubicin, daunorubicin and/or doxorubicin transport systems in rat polymorphonuclear leukocyt
Autor:
Teruyoshi Yokoyama, Katsuhiko Okumura, Noriaki Ohnishi, Kazuki Nagasawa, Masako Nomiyama, Seigo Iwakawa
Publikováno v:
Biologicalpharmaceutical bulletin. 17(5)
The characteristics of pirarubicin transport have been investigated in polymorphonuclear leukocytes isolated from rats. The uptake of pirarubicin by leukocytes was time-, temperature- and concentration-dependent with the maximum velocity (Vmax) of 4.