Castration prevents calcium channel blocker-induced gingival hyperplasia in beagle dogs

被引:10
作者
Dayan, D [1 ]
Kozlovsky, A
Tal, K
Kariv, N
Shemesh, M
Nyska, A
机构
[1] Tel Aviv Univ, Maurice & Gabriela Goldschleger Sch Dent Med, Dept Oral Pathol & Oral Med, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Maurice & Gabriela Goldschleger Sch Dent Med, Dept Periodontol, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[4] Hebrew Univ Jerusalem, Beit Dagan & Koret Sch Vet Med, Kimron Vet Inst, Dept Hormone Res, Jerusalem, Israel
[5] NIEHS, Res Triangle Pk, NC 27709 USA
关键词
castration; calcium channel-blocker; gingival hyperplasia;
D O I
10.1191/096032798678908945
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
1 The purpose of this study was to investigate testosterone's role on the calcium channel antagonist oxodipine-inducing gingival hyperplasia in a dog model. 2 Two experiments were conducted using castrated and intact male dogs. Oxodipine was administered orally for 90 days, at a dose of 24 mg/kg/day. In the first experiment, the occurrence of gingival hyperplasia was evaluated. In the second, the gingival index (GI) and gingival hyperplasia index (GHI) were recorded and correlated with serum levels of testosterone. 3 A significant positive correlation between GI, GHI and plasma testosterone was noted, Castrated dogs were injected with testosterone, 4 months after the start of oxodipine treatment, while in the non-castrated dogs, administration of oxodipine was stopped. Castration correlated with lack of GH, while testosterone injection to the same dogs was associated with an increase of GI and GHI. 4 Since it is known that testosterone receptors are present in the gingiva, ii is proposed that oxodipine-induced gingival hyperplasia could be mediated by the calcium channel blocker on plasma testosterone levels.
引用
收藏
页码:396 / 402
页数:7
相关论文
共 33 条
[1]   RISK-FACTORS IN PHENYTOIN-INDUCED GINGIVAL HYPERPLASIA [J].
ADDY, V ;
MCELNAY, JC ;
EYRE, DG ;
CAMPBELL, N ;
DARCY, PF .
JOURNAL OF PERIODONTOLOGY, 1983, 54 (06) :373-377
[2]   INDUCTION OF SKIN AND THYROID-TUMORS IN MALE-RATS BY NORMAL-METHYL-NORMAL-NITROSOUREA AFTER SEQUENTIAL TREATMENT WITH CYPROTERONE-ACETATE AND TESTOSTERONE PROPIONATE - EFFECTS OF CASTRATION, RAT STRAIN AND TIME OF CARCINOGEN INJECTION [J].
BOSLAND, MC ;
PRINSEN, MK ;
RIVENSON, A ;
WEISBURGER, JH .
CARCINOGENESIS, 1992, 13 (04) :669-674
[3]   THE MITOGENIC ACTIONS OF TESTOSTERONE PROPIONATE AND OF OESTRONE ON THE EPIDERMIS OF THE ADULT MALE MOUSE [J].
BULLOUGH, WS ;
VANOORDT, GJ .
ACTA ENDOCRINOLOGICA, 1950, 4 (03) :291-305
[4]  
CRANE SW, 1984, CURRENT TECHNIQUES S, P369
[5]   SALIVARY TESTOSTERONE MEASUREMENTS - RELIABILITY ACROSS HOURS, DAYS, AND WEEKS [J].
DABBS, JM .
PHYSIOLOGY & BEHAVIOR, 1990, 48 (01) :83-86
[6]   SALIVARY TESTOSTERONE MEASUREMENTS - COLLECTING, STORING, AND MAILING SALIVA SAMPLES [J].
DABBS, JM .
PHYSIOLOGY & BEHAVIOR, 1991, 49 (04) :815-817
[7]   SALIVARY TESTOSTERONE MEASUREMENTS IN BEHAVIORAL-STUDIES [J].
DABBS, JM .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1993, 694 :177-183
[8]  
DAYAN D, 1993, INT J EXP PATHOL, V74, P225
[9]   RELATIONSHIP BETWEEN DNA FRAGMENTATION AND APOPTOSIS IN THE PROGRAMMED CELL-DEATH IN THE RAT PROSTATE FOLLOWING CASTRATION [J].
ENGLISH, HF ;
KYPRIANOU, N ;
ISAACS, JT .
PROSTATE, 1989, 15 (03) :233-250
[10]  
GALIANO A, 1987, DRUGS FUTURE, V12, P623