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环孢素A与硝苯地平或地尔硫䓬联合口服治疗对大鼠药物性牙龈增生的影响。

Effects of combined oral treatments with cyclosporine A and nifedipine or diltiazem on drug-induced gingival overgrowth in rats.

作者信息

Morisaki I, Fukui N, Fujimori Y, Murakami J, Daikoku H, Amano A

机构信息

Division of Special Care Dentistry, Osaka University Faculty of Dentistry, Japan.

出版信息

J Periodontol. 2000 Mar;71(3):438-43. doi: 10.1902/jop.2000.71.3.438.

Abstract

BACKGROUND

Cyclosporine A (CsA) and calcium channel blockers induce gingival overgrowth in humans and animals. Recently, nifedipine and diltiazem have often been used to control CsA-related hypertension in organ transplant patients. The purpose of this study was to examine the effects of a combined oral treatment of CsA and nifedipine or diltiazem on the severity of gingival overgrowth in rats.

METHODS

Fifteen-day-old Fischer rats were treated orally with single or combined applications of CsA, nifedipine, and/or diltiazem for 40 days; and induced gingival overgrowth, rat growth, and blood drug levels were compared among the different experimental groups. The experiment consisted of 6 groups: one control group (group A) and 5 test groups treated with CsA (group B), nifedipine (group C), and diltiazem (group D), as well as those concurrently treated with CsA and nifedipine (group E), and CsA and diltiazem (group F). Gingival overgrowth was determined by measuring the depth of the gingival sulcus.

RESULTS

The mandibular buccal gingival sulcus depth of group A was 365 +/- 41.2 microm. Among the test groups, the most remarkable gingival overgrowth was seen in group E (1,020 +/- 63.3 microm), followed by group F (895 +/- 43.8 microm), group B (870 +/- 48.3 microm), group C (525 +/- 116 microm), and then group D (505 +/- 83.2 microm). Rat body weight gain was reduced significantly by oral CsA treatment. Neither nifedipine nor diltiazem suppressed rat growth when used independently; however, rat growth reduced by CsA was further suppressed by a combined use of diltiazem, but not nifedipine. CsA blood levels were reduced by concurrent oral treatment with nifedipine or diltiazem along with the blood levels of those calcium channel blockers when treatment was in combination with CsA.

CONCLUSIONS

These results suggest that gingival overgrowth is induced in rats as a side effect of CsA, nifedipine, or diltiazem, and the combined use of these drugs influences rat growth, blood drug levels, and the severity of gingival overgrowth.

摘要

背景

环孢素A(CsA)和钙通道阻滞剂可在人和动物中引起牙龈增生。最近,硝苯地平和地尔硫䓬常用于控制器官移植患者中与CsA相关的高血压。本研究的目的是研究CsA与硝苯地平或地尔硫䓬联合口服治疗对大鼠牙龈增生严重程度的影响。

方法

15日龄的Fischer大鼠经口给予CsA、硝苯地平及/或地尔硫䓬单一或联合用药40天;比较不同实验组之间的牙龈增生、大鼠生长及血药浓度。实验分为6组:1个对照组(A组)和5个试验组,分别用CsA(B组)、硝苯地平(C组)、地尔硫䓬(D组)治疗,以及同时用CsA和硝苯地平(E组)、CsA和地尔硫䓬(F组)治疗。通过测量牙龈沟深度确定牙龈增生情况。

结果

A组下颌颊侧牙龈沟深度为365±41.2微米。在试验组中,E组牙龈增生最为显著(1020±63.3微米),其次是F组(895±43.8微米)、B组(870±48.3微米)、C组(525±116微米),然后是D组(505±83.2微米)。口服CsA治疗可显著降低大鼠体重增加。单独使用硝苯地平和地尔硫䓬均未抑制大鼠生长;然而,地尔硫䓬与CsA联合使用可进一步抑制CsA降低的大鼠生长,而硝苯地平则无此作用。与CsA联合治疗时,硝苯地平或地尔硫䓬与CsA同时口服可降低CsA血药浓度,同时也会降低这些钙通道阻滞剂的血药浓度。

结论

这些结果表明,CsA、硝苯地平或地尔硫䓬作为副作用可在大鼠中引起牙龈增生,这些药物的联合使用会影响大鼠生长、血药浓度及牙龈增生的严重程度。

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