二乙基卡马嗪对卡氏石蛾体内外微丝的影响。

D J Weiner, D Abraham, R D'Antonio
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引用次数: 2

摘要

采用体外和体内系统研究了二乙基卡马嗪(DEC)对培养的carinii Litomosoides microfilariae (MFF)的影响。体内实验:同龄雄性大鼠Mastomys natalensis,分别胸腔(12)或腹腔(36)注射10(3)或10(4)MFF。30 min后,每组各取1 / 2大鼠给予DEC。在给药后30、60和120分钟,治疗组和未治疗组各2只大鼠出血并死亡。用温盐水(0.15 M NaCl)冲洗胸膜或腹膜腔以回收MFF。在胸腔内和腹腔内实验中,治疗组和对照组在30和120分钟时回收的MFF数量相同。然而,在60分钟时,治疗组的MFF数量比未治疗组少85.5%。血液中没有发现MFF。体外:将MFF加入到组织培养皿中(Linbro Div., Flow Labs, Hamden, Conn),制备如下:DEC-血清(正常大鼠给予DEC 500 mg/kg的血清)、DEC +血清(添加DEC的血清)、仅血清、仅RPMI 1640和RPMI 1640 + DEC。此外,五种处理分别制备或不制备未刺激的腹膜渗出(PE)细胞。在dec -血清孔中30分钟,45%的MFF有粘附的PE细胞;在其余的孔中,这些细胞粘附在11%或更少的MFF上。我们将上述现象解释为DEC处理感染L. carinii的M. natalensis后捕获和消除MFF的第一步。
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The effect of diethylcarbamazine on microfilariae of Litomosoides carinii in vitro and in vivo.

Culture-derived Litomosoides carinii microfilariae (MFF) were used in in vitro and in vivo systems to investigate the effect of diethylcarbamazine (DEC) on these MFF. In vivo: Male rats, Mastomys natalensis, all of the same age, were injected intrathoracically (12) or intraperitoneally (36) with 10(3) or 10(4) MFF. After 30 min one half of each group of rats was given DEC per os. At 30, 60, and 120 min after DEC administration, two rats from the treated and two from the untreated group were bled and killed. The pleural or peritoneal cavities were rinsed with warm saline (0.15 M NaCl) to recover MFF. In both the intrathoracic and intraperitoneal experiments, equal numbers of MFF were recovered from treated and control rats at 30 and 120 min. However, at 60 min 85.5% fewer were recovered from the treated than from the nontreated animals. MFF were not found in the blood. In vitro: MFF were added to tissue culture dish wells (Linbro Div., Flow Labs, Hamden, Conn) prepared as follows: DEC-Serum (serum from normal rats given DEC at 500 mg/kg), DEC + Serum (serum with added DEC), serum only, RPMI 1640 only, and RPMI 1640 + DEC. Furthermore, the five treatments were prepared either with or without unstimulated peritoneal exudate (PE) cells. At 30 min in the DEC-Serum wells 45% of the MFF had adherent PE cells; in the remaining wells these cells adhered to 11% or fewer MFF. We interpret the aforementioned phenomena as representing the first step in the trapping and elimination of MFF after DEC treatment of L. carinii-infected M. natalensis.

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