Borovsky D, Carlson D A, Ujváry I
Institute of Food and Agricultural Sciences, University of Florida, Vero Beach 32692.
J Med Entomol. 1992 Jul;29(4):619-29. doi: 10.1093/jmedent/29.4.619.
Biosynthesis and metabolism of juvenile hormone (JH) III in vivo and in vitro were studied in female Aedes aegypti (L.). [12-3H]Methyl farnesoate was used to follow the synthesis and [12-3H]-(10R)-JH III to study metabolism. The rate of biosynthesis of [12-3H]JH III in vivo after adult eclosion increased from 9 fmol/h per female at 1 h to 22 fmol/h per female at day 6. The rate of biosynthesis by exposed corpora allata (CA) in vitro was 23 fmol/h per CA during the 1st d after adult eclosion, then dropped to 4.8 fmol/h per CA on day 3, then increased again to a constant level of synthesis (12 fmol/h per CA) at days 4-6. Immediately after blood feeding, the rate of synthesis of [12-3H]JH III in vivo and in vitro increased to 27 fmol/h per female and to 23 fmol/h per CA, respectively. The rate of synthesis then decreased in vivo to 12 fmol/h per female at 4 h and in vitro to 6 fmol/h per CA 10 h after the blood meal. After this decrease, the rate of synthesis of [12-3H]JH III increased again reaching a peak of 25 fmol/h per female at 48-96 h in vivo and 12 fmol/h per CA at 72 h in vitro. These results indicated that the CA of sugar-fed and blood-fed female A. aegypti synthesized JH III in vivo and in vitro from [12-3H]methyl farnesoate. When [12-3H]-(10R)-JH III metabolism was followed in vivo in female A. aegypti, the ratio between JH III diol acid:JH III acid:JH III diol was 17:4:1, indicating that JH III was first hydrolyzed by JH III esterase to the acid form, then hydrated to the diol acid by JH III epoxide hydrase. Females treated with [12-3H]JH III acid converted 46% of the JH III acid in 60 min to the diol acid. These results indicated that the enzyme epoxide hydrase acted on JH III acid 17 times faster than JH III.
在雌性埃及伊蚊体内和体外研究了保幼激素(JH)III的生物合成与代谢。[12-³H]法尼酸甲酯用于追踪合成过程,[12-³H]-(10R)-JH III用于研究代谢。羽化后体内[12-³H]JH III的生物合成速率从羽化后1小时的每只雌蚊9飞摩尔/小时增加到第6天的每只雌蚊22飞摩尔/小时。羽化后第1天,离体的咽侧体(CA)在体外的生物合成速率为每个CA 23飞摩尔/小时,然后在第3天降至每个CA 4.8飞摩尔/小时,之后在第4至6天再次增加至恒定的合成水平(每个CA 12飞摩尔/小时)。刚吸血后,体内和体外[12-³H]JH III的合成速率分别增加到每只雌蚊27飞摩尔/小时和每个CA 23飞摩尔/小时。然后合成速率在体内于吸血后4小时降至每只雌蚊12飞摩尔/小时,在体外于吸血后10小时降至每个CA 6飞摩尔/小时。此次下降后,[12-³H]JH III的合成速率再次增加,在体内48至96小时达到每只雌蚊25飞摩尔/小时的峰值,在体外72小时达到每个CA 12飞摩尔/小时的峰值。这些结果表明,取食糖水和吸血的雌性埃及伊蚊的咽侧体在体内和体外均能从[12-³H]法尼酸甲酯合成JH III。当在雌性埃及伊蚊体内追踪[12-³H]-(10R)-JH III的代谢时,JH III二醇酸:JH III酸:JH III二醇的比例为17:4:1,这表明JH III首先被JH III酯酶水解为酸形式,然后被JH III环氧水解酶水合为二醇酸。用[12-³H]JH III酸处理的雌蚊在60分钟内将46%的JH III酸转化为二醇酸。这些结果表明,环氧水解酶作用于JH III酸的速度比作用于JH III的速度快17倍。