TY - JOUR
T1 - Effect of prenatal vitamin D (calcitriol) exposure on the growth and development of the prostate
AU - Konety, Badrinath R.
AU - Nangia, Ajay K.
AU - Nguyen, Thu Song T.
AU - Thomas, Angela
AU - Getzenberg, Robert H.
PY - 1999
Y1 - 1999
N2 - BACKGROUND. We previously found that in the absence of testosterone (T), calcitriol promotes proliferation of normal prostatic stroma, while in the presence of T, it has a differentiating effect on prostatic epithelium. The present study was conducted to determine the effect of calcitriol exposure in utero on the postnatal development of the normal prostate. METHODS. Pregnant rats were injected subcutaneously with either l.25 μg of calcitriol or vehicle alone on alternate days till delivery. Calcitriol-exposed and control pups were sacrificed at age 25 days (prepuberty), 63 days (postpuberty), or 102 days (adults), and their prostates and seminal vesicles were harvested find weighed. RESULTS. Pups prenatally exposed to calcitriol and sacrificed before puberty (25 days) had a 35% greater mean prostatic weight than controls (0.0314 vs. 0.0422 g, P < 0.007), and calcitriol-exposed adult rats (102 days) had a 68% greater mean prostatic weight than controls (0.1365 vs. 0.2304 g, P < 0.005). No differences were observed in seminal vesicle weights, and in serum calcium and testosterone levels. A disproportionately high mortality rate from sudden death (71%) was observed at puberty in uncastrated male rats prenatally exposed to calcitriol. CONCLUSIONS. These findings suggest that high-dose calcitriol exposure in utero may uniquely influence subsequent prostatic growth. Nonandrogenic steroids such as calcitriol may also be involved in genetic imprinting of the prostate.
AB - BACKGROUND. We previously found that in the absence of testosterone (T), calcitriol promotes proliferation of normal prostatic stroma, while in the presence of T, it has a differentiating effect on prostatic epithelium. The present study was conducted to determine the effect of calcitriol exposure in utero on the postnatal development of the normal prostate. METHODS. Pregnant rats were injected subcutaneously with either l.25 μg of calcitriol or vehicle alone on alternate days till delivery. Calcitriol-exposed and control pups were sacrificed at age 25 days (prepuberty), 63 days (postpuberty), or 102 days (adults), and their prostates and seminal vesicles were harvested find weighed. RESULTS. Pups prenatally exposed to calcitriol and sacrificed before puberty (25 days) had a 35% greater mean prostatic weight than controls (0.0314 vs. 0.0422 g, P < 0.007), and calcitriol-exposed adult rats (102 days) had a 68% greater mean prostatic weight than controls (0.1365 vs. 0.2304 g, P < 0.005). No differences were observed in seminal vesicle weights, and in serum calcium and testosterone levels. A disproportionately high mortality rate from sudden death (71%) was observed at puberty in uncastrated male rats prenatally exposed to calcitriol. CONCLUSIONS. These findings suggest that high-dose calcitriol exposure in utero may uniquely influence subsequent prostatic growth. Nonandrogenic steroids such as calcitriol may also be involved in genetic imprinting of the prostate.
KW - Animal experiments
KW - Fetal exposure
KW - Prostate development
KW - Vitamin D
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U2 - 10.1002/(SICI)1097-0045(19991101)41:3<181::AID-PROS5>3.0.CO;2-7
DO - 10.1002/(SICI)1097-0045(19991101)41:3<181::AID-PROS5>3.0.CO;2-7
M3 - Article
C2 - 10517876
AN - SCOPUS:0032707977
SN - 0270-4137
VL - 41
SP - 181
EP - 189
JO - Prostate
JF - Prostate
IS - 3
ER -