Navarro H A, Seidler F J, Schwartz R D, Baker F E, Dobbins S S, Slotkin T A
Department of Pharmacology, Duke University Medical Center, Durham, NC 27710.
Brain Res Bull. 1989 Sep;23(3):187-92. doi: 10.1016/0361-9230(89)90146-9.
Prenatal exposure to high doses of nicotine (greater than 6 mg/kg/day) via maternal infusions has been shown to impair nervous system development and to decrease viability and growth. In the current study, we have examined the effects of infusing pregnant rats with 2 mg/kg of nicotine per day from gestational days 4 through 20. At this lower dose, there was neither interference with maternal weight gain nor any increase in resorption rate. Intrauterine and postnatal growth was maintained at normal or supranormal rates in the exposed offspring. Nevertheless, sufficient nicotine penetrated the fetal brain to cause persistent alterations in [3H]nicotine binding sites, abnormalities of cellular development [assessed by measurements of ornithine decarboxylase (ODC) activity and deoxyribonucleic acid (DNA)], and impairment of development of peripheral noradrenergic projections (assessed by kidney norepinephrine levels); in each case, the neural alterations were virtually equivalent to those obtained previously at the higher, growth-suppressant dosage. These findings indicate that growth impairment alone is insufficient to predict the adverse effects of nicotine on development.
通过母体输注对孕期大鼠进行高剂量尼古丁暴露(大于6毫克/千克/天)已被证明会损害神经系统发育,并降低存活率和生长速度。在本研究中,我们检测了从妊娠第4天至第20天每天给怀孕大鼠输注2毫克/千克尼古丁的影响。在这个较低剂量下,既没有干扰母体体重增加,吸收率也没有任何升高。暴露组后代的子宫内和产后生长维持在正常或超常速率。然而,足够的尼古丁穿透胎儿大脑,导致[3H]尼古丁结合位点持续改变、细胞发育异常[通过鸟氨酸脱羧酶(ODC)活性和脱氧核糖核酸(DNA)测量评估]以及外周去甲肾上腺素能投射发育受损(通过肾脏去甲肾上腺素水平评估);在每种情况下,神经改变实际上与先前在较高的、抑制生长剂量下获得的改变相当。这些发现表明,仅生长受损不足以预测尼古丁对发育的不良影响。