D. Dayan et al., CASTRATION PREVENTS CALCIUM-CHANNEL BLOCKER-INDUCED GINGIVAL HYPERPLASIA IN BEAGLE DOGS, Human & experimental toxicology, 17(7), 1998, pp. 396-402
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 i
ntact male dogs. Oxodipine was administered orally for 90 days, at a d
ose of 24 mg/kg/day. In the first experiment, the occurrence of gingiv
al hyperplasia was evaluated. In the second, the gingival index (GI) a
nd gingival hyperplasia index (GHI) were recorded and correlated with
serum levels of testosterone. 3 A significant positive correlation bet
ween GI, GHI and plasma testosterone was noted, Castrated dogs were in
jected with testosterone, 4 months after the start of oxodipine treatm
ent, while in the non-castrated dogs, administration of oxodipine was
stopped. Castration correlated with lack of GH, while testosterone inj
ection 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 gin
giva, ii is proposed that oxodipine-induced gingival hyperplasia could
be mediated by the calcium channel blocker on plasma testosterone lev
els.