Re. Poland et al., EXPOSURE TO THRESHOLD DOSES OF NICOTINE IN-UTERO .2. NEUROENDOCRINE RESPONSE TO NICOTINE IN ADULT MALE OFFSPRING, Developmental brain research, 83(2), 1994, pp. 278-284
Groups of gravid female rats were injected subcutaneously with saline
(SAL), a low-dose of nicotine (LN) (0.05 mg/kg, bid) or a high-dose of
nicotine (HN) (3.0 mg/kg, bid) from day 4 to day 20 of gestation, or
were left undisturbed. In adult 120-day-old male offspring, the ACTH a
nd prolactin responses to acute nicotine challenge were evaluated. The
experiment was performed on three separate occasions. Based upon dose
-response and time-course studies with nicotine in normal animals, the
neuroendocrine responses to nicotine (0.75 and 1.0 mg/kg, sc) were me
asured 7.5 min after nicotine administration, the peak response-time f
or both hormones. The ACTH response to acute nicotine administration w
as blunted significantly in the HN rats, but normal in the LN rats, fo
r all three experiments. In two experiments, the prolactin response to
acute nicotine administration was blunted significantly in the HN rat
s, but enhanced significantly in the LN offspring. The results indicat
e that prenatal nicotine administration can produce long-term neuroend
ocrine effects involving nicotinic-receptor coupled circuits, with lon
g-term functional sequelae produced by dosages of nicotine considerabl
y smaller than previously shown to be pharmacologically/toxicologicall
y active.