Sekine H, Nagao S, Nakahara Y
Criminal Investigation Laboratory, Saitama Pref. Police H.Q., Japan.
Biol Pharm Bull. 1996 Jun;19(6):845-51. doi: 10.1248/bpb.19.845.
N-Cyanomethylmethamphetamine (CMMA), N-formylmethamphetamine (FMA) and methamphetamine (MA) were given intraperitoneally to mouse and rat in doses of 3 mg/kg. The major metabolites of CMMA, FMA and MA in plasma were determined at short intervals after administration by GC-MS to obtain the area under the concentration-time curve (AUC). Regarding the plasma concentration of FMA after CMMA administration, a definite species difference was observed between mouse and rat. In rats given CMMA, FMA was the major component, followed by MA, amphetamine (AP), CMMA and N-formylamphetamine (FAP). In mice given CMMA, MA was a major component, followed by AP, FMA, CMMA and FAP. However, it was demonstrated that MA is also non-enzymatically produced from CMMA in plasma. Following FMA administration to rats, FMA was the major component in the plasma, showing the largest AUC value of the four metabolites, FMA, FAP, MA and AP. Following FMA administration to mice, MA showed the largest AUC value, followed by FMA, FAP and AP which were present at low levels even 5 min after injection and were scarcely detectable at 60 min. These results suggest two main mechanisms involved in the metabolism of the N-cyanomethyl group, one of which is the formation of MA by elimination of cyanoformaldehyde from N-alpha-hydroxylated CMMA and the other which is the formation of FMA by elimination of hydrogen cyanide from N-alpha-hydroxylated CMMA. The formation of FMA from CMMA was the predominant pathway in rats but not in mice.
将N-氰甲基甲基苯丙胺(CMMA)、N-甲酰基甲基苯丙胺(FMA)和甲基苯丙胺(MA)以3mg/kg的剂量腹腔注射给小鼠和大鼠。给药后短时间内,通过气相色谱-质谱联用仪(GC-MS)测定血浆中CMMA、FMA和MA的主要代谢产物,以获得浓度-时间曲线下面积(AUC)。关于CMMA给药后血浆中FMA的浓度,在小鼠和大鼠之间观察到明显的种属差异。给大鼠注射CMMA后,FMA是主要成分,其次是MA、苯丙胺(AP)、CMMA和N-甲酰基苯丙胺(FAP)。给小鼠注射CMMA后,MA是主要成分,其次是AP、FMA、CMMA和FAP。然而,已证明MA也可在血浆中由CMMA非酶促产生。给大鼠注射FMA后,FMA是血浆中的主要成分,其AUC值在四种代谢产物FMA、FAP、MA和AP中最大。给小鼠注射FMA后,MA的AUC值最大,其次是FMA、FAP和AP,它们在注射后5分钟时含量就很低,在60分钟时几乎检测不到。这些结果表明,N-氰甲基基团的代谢涉及两种主要机制,其中一种是通过从N-α-羟基化的CMMA中消除氰基甲醛形成MA,另一种是通过从N-α-羟基化的CMMA中消除氰化氢形成FMA。由CMMA形成FMA是大鼠中的主要途径,但在小鼠中并非如此。