GESTATIONAL EXPOSURE TO LOUD NOISE ALTERS THE DEVELOPMENT AND POSTNATAL RESPONSIVENESS OF HUMORAL AND CELLULAR-COMPONENTS OF THE IMMUNE-SYSTEM IN OFFSPRING
Sk. Sobrian et al., GESTATIONAL EXPOSURE TO LOUD NOISE ALTERS THE DEVELOPMENT AND POSTNATAL RESPONSIVENESS OF HUMORAL AND CELLULAR-COMPONENTS OF THE IMMUNE-SYSTEM IN OFFSPRING, Environmental research, 73(1-2), 1997, pp. 227-241
Gestational exposure of the female to environmental toxins can alter i
mmune function in the offspring. We have recently shown that prenatal
maternal stress, that is, stress applied to or induced in the female d
uring pregnancy, can also alter the development of humoral immunocompe
tence in the offspring and their hormonal. and immunologic responses t
o postnatal stress. This report presents data from two experiments on
the effects of prenatal exposure to loud noise-prenatal sound stress (
PSS)-on the development and responsiveness of in vitro and in vivo hum
oral and cellular immune function in the offspring. Pregnant rats were
exposed daily from Day 15 to Day 21 of gestation to an inescapable lo
ud noise (an 85- to 90-decibel fire alarm bell) delivered randomly for
1 hr. In developing offspring, PSS produced age-dependent and mitogen
-specific alterations in lymphoproliferative activity and reduced immu
noglobulin G levels at Postnatal Day 21. Antibody titers to herpes sim
plex virus type I were also reduced. Exposure to loud noise before or
after infection produced an additional reduction in titers in these of
fspring. Arthus skin reaction (AR) to old tuberculin was reduced by PS
S. Combined prenatal/postnatal sound stress further reduced this respo
nse and the AR to bovine serum albumin (BSA). Delayed hypersensitivity
reaction to BSA was reduced in PSS offspring; postnatal sound stress
enhanced the reaction to both antigens, but only in males. Antibody ti
ters to BSA were increased by PSS; adjuvant-induced inflammation was a
ttenuated by postnatal sound stress. These data suggest that in utero
exposure to loud noise, which can occur in the workplace, is toxic to
the developing immune system. (C) 1997 Academic Press.