Biol. Pharm. Bull. 28(1) 151—153 (2005)

نویسندگان

  • Yuji YOSHIYAMA
  • Motoko KANKE
چکیده

is related to the imidazole. A long half-life permits once daily dosing. The mechanism of action of fluconazole is similar to that of other imidazole and triazole antifungal agents, specifically, the inhibition of cytochrome P-450-dependent ergosterol synthesis. The drug is effective when administered orally and intravenously for a variety of fungal infections, especially cryptococcosis in acquired immunodeficiency syndrome patients. Case reports have described QT prolongation and torsades de points associated with fluconazole. The concurrent administration of Class I antiarrhythmic agents and agents that prolong the QT interval, such as fluconazole, may increase the risk of cardiotoxicity. The toxicological and pharmacological effects of cardiovascular drugs are usually studied in mammals and the results obtained are extrapolated to humans. Chick embryonic heart develops through a similar process to that in mice, rats and humans, and also has a similar atrioventricular system. Chick embryos have been widely used in pharmacologic and toxicologic experiments for evaluating drug action on the fetus. With the recent concern for animal rights, experimental studies using mammals have been limited in number and methods. Thus, based on social acceptance, experimental studies using chick embryos have drawn attention. To develop alternative methods, we have studied the biologic effects of drugs on the cardiovascular system of chick embryos using physiologic techniques. And we have also reported that the chick embryonic model of hypothyrodism produced by treatment with thiamazole can be used to examine the pharmacological and toxicological effects of cardiovascular drugs. Drug drug interactions have been demonstrated for a variety of drugs, including disopyramide and propranolol, in the heart failure patients. We have evaluated the toxic interactions between propranolol and disopyramide in chick embryos. Toxic interaction between fluconazole and disopyramide may result in additive effects on QT prolongation. The present study evaluated the effect of fluconazole on the heart and the toxic interactions between fluconazole and disopyramide in chick embryos.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Biol. Pharm. Bull. 28(3) 563—564 (2005)

Tomomi NOGUCHI, Chihiro SHINJI, Hisayoshi KOBAYASHI, Makoto MAKISHIMA, Hiroyuki MIYACHI, and Yuichi HASHIMOTO* Institute of Molecular & Cellular Biosciences, The University of Tokyo; 1–1–1 Yayoi, Bunkyo-ku, Tokyo 113–0032, Japan: and Department of Biochemistry, Nihon University, School of Medicine; 30–1 Oyaguchi-kamicho, Itabashi-ku, Tokyo 173–8610, Japan. Received January 13, 2005; accepted Ja...

متن کامل

Biol. Pharm. Bull. 28(10) 2026—2027 (2005)

Shuso TAKEDA, Yuji ISHII, Peter I. MACKENZIE, Kiyoshi NAGATA, Yasushi YAMAZOE, Kazuta OGURI, and Hideyuki YAMADA* a Graduate School of Pharmaceutical Sciences, Kyushu University; Fukuoka 812–8582, Japan: b Department of Clinical Pharmacology, Flinders Medical Centre and Flinders University; Adelaide, SA5042, Australia: c Graduate School of Pharmaceutical Sciences, Tohoku University; Sendai 980–...

متن کامل

Biol. Pharm. Bull. 28(5) 937—939 (2005)

a Laboratory of Medicinal Pharmacognosy, Tokyo University of Pharmacy and Life Science, School of Pharmacy, 1432–1 Horinouchi, Hachioji, Tokyo 192–0392, Japan: b Functional Foods Development Division, Kaneka Corporation; Takasago, Hyogo 676–8688, Japan: c Life Science Research Laboratories, Life Science RD Center, Kaneka Corporation; Takasago, Hyogo 676–8688; Japan: d Division of Molecular Meta...

متن کامل

Chem. Pharm. Bull. 53(2) 153—163 (2005)

derivatives (Fig. 1) that showed in vitro and in vivo antitumor activity. These compounds were also found to inhibit tubulin polymerization as a mechanism of their action in cells. To investigate the possibilities for modification of this scaffold, we divided the moieties into five parts from A to E as shown in Fig. 1. So far, it has been reported that the length of the three carbon chain on mo...

متن کامل

Biol. Pharm. Bull. 28(2) 374—377 (2005)

cales) are known to contain structurally unique secondary metabolites, such as plastoquinones, chromanols, a cyclopentenone, and polysaccharides. These compounds show various biological activities due to their unique structure. We previously reported that the methanolic extract of the brown alga, Sargassum micracanthum (KUETZING) ENDLICHER, “Togemoku” in Japanese, showed strong antioxidant acti...

متن کامل

Biol. Pharm. Bull. 28(4) 768—771 (2005)

Rat pheochromocytoma PC12 cells undergo neuronal differentiation in response to nerve growth factor. We show here that exposure of PC12 cells to Nardostachys chinensis glycoside induces the outgrowth of neurites, increases the activity of AChE, triggers cell cycle arrest in G1 and enhances the expression of growth associated protein 43 (GAP-43). Both the outgrowth of neurites and the increase i...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2004