Yonaga T, Fujino Y, Tamura R, Kurabayashi K, Uraya T, Aono K, Yoshimura K
Anat Anz. 1985;159(1-5):373-83.
The pharmacological effects of methyl mercury chloride (MMC) and mercuric chloride (HgCl2) (2-16 mg/Kg per day subcutaneously, for 6 d) upon the growth were studied in the incisors and proximal tibiae of immature rats histologically. Lead acetate was used as a time marker. 1. Mercury compounds slightly affected the body weight gains of the rats but apparently inhibited the longitudinal growth of proximal tibia and the effect increased with higher dosages. 2. Mercury compounds definitely inhibited not only the longitudinal growth (incisor growth) but also the appositional growth (dentin formation) of incisal dentin. 3. The inhibitory effect on the growth was ranked as follows: bone growth greater than dentin formation greater than incisor growth. 4. The actions of MMC on the growth of incisors and proximal tibiae appeared gradually and the response was biphasic; stimulatory and then inhibitory. The inhibitory effect appeared even after the injection was discontinued and appeared more extremely than during the injections. 5. In HgCl2 groups the inhibitory effect on the growth appeared rapidly. The effect increased with higher dosages and became stronger as the injections were repeated. However, this effect was weakened promptly after the injection was discontinued. 6. The repeated injections of mercury compounds hardly affected the level of serum calcium but disturbed the calcification of incisal dentin. From the above-mentioned results a possible mechanism was discussed. It is suggestive that MMC acts directly upon a cell and is transported into it. Once MMC was introduced into a cell it is slowly demethylated to inorganic Hg and acts as the demethylated mercury. When accumulated mercury is slight in volume, it stimulates and then inhibits the cell function with increasing mercury. However HgCl2 binds directly with an effector cell membrane in loose fashion. This may cause the ready reversibility of the effect.
对未成熟大鼠皮下注射氯化甲基汞(MMC)和氯化汞(HgCl2)(每天2 - 16毫克/千克,共6天),通过组织学方法研究了其对大鼠切牙和胫骨近端生长的药理作用。使用醋酸铅作为时间标记物。1. 汞化合物对大鼠体重增加影响轻微,但明显抑制胫骨近端的纵向生长,且随着剂量增加抑制作用增强。2. 汞化合物不仅明确抑制切牙的纵向生长(切牙生长),还抑制切牙牙本质的附着生长(牙本质形成)。3. 对生长的抑制作用排序如下:骨骼生长大于牙本质形成大于切牙生长。4. MMC对切牙和胫骨近端生长的作用逐渐显现,且反应呈双相;先是刺激,然后是抑制。即使停止注射,抑制作用仍会出现,且比注射期间更为明显。5. 在HgCl2组中,对生长的抑制作用迅速出现。随着剂量增加,作用增强,且随着注射次数增多而更强。然而,停止注射后这种作用迅速减弱。6. 重复注射汞化合物对血清钙水平影响不大,但会干扰切牙牙本质的钙化。根据上述结果讨论了可能的机制。提示MMC直接作用于细胞并被转运入细胞内。一旦MMC进入细胞,它会缓慢脱甲基化为无机汞,并以脱甲基汞的形式起作用。当积累的汞量较少时,它会随着汞含量增加先刺激然后抑制细胞功能。然而,HgCl2以松散的方式直接与效应细胞膜结合。这可能导致作用易于逆转。