Mm. Koller et al., Desipramine induced changes in salivary proteins, cultivable oral microbiota and gingival health in aging female NIA Fischer 344 rats, LIFE SCI, 68(4), 2000, pp. 445-455
Cyclic antidepressants are still a dominating group of psychotherapeutic dr
ugs used in the treatment of depression. One of their major side effect is
salivary gland dysfunction (oral dryness, xerostomia), leading in humans to
increased oral disease and dysfunction of speech, chewing, swallowing and
taste. The purpose of this study was to assess the effects of the long-term
administration of the tricyclic antidepressant desipramine and the reversi
bility of this treatment following a 15 d washout period on specific saliva
ry proteins, composition of oral microbiota, and oral health (gingivitis) o
f aging female F344 rats. Total salivary proteins showed decreased concentr
ations with age and desipramine. Similar SDS/PAGE protein profiles appeared
in all phases but in different relative amounts with age and treatment. Wh
ile certain proteins maintained steady levels (lactoferrin) or decreased wi
th age and treatment (amylase), the synthesis of proline-rich proteins, hig
h molecular weight mucin-type glycoproteins, and lysozyme was induced with
desipramine and age. The oral microbiota was significantly changed with age
and the administration of the antidepressant. The incidence of gingivitis
with desipramine was highest in the oldest animals. For the different param
eters measured, recovery was delayed with age. These data indicate, that de
sipramine has profound effects on salivary protein secretion. This may part
ially explain the changes in microbiota and the increased incidence of ging
ivitis. (C) 2000 Elsevier Science Inc. All rights reserved.