TABLE 2.
Clinical | ||||
Study type | Gender % (♂/♀) | Developmental stage at test | Finding | References |
Retrospective cohort | Not stated | 3 years | PTE in boys (heavy exposure) → Increased risk of conduct-only problems, hyperactivity-inattention only problems, and co-occurring problems. PTE in girls (light and heavy exposure) → Increased risk of conduct-only problems. PTE in boys → increased hyperactivity–inattention and conduct problems. PTE in girls → increased conduct-only problems. |
Hutchinson et al., 2010 |
Prospective cohort | 52/48 | 4, 12, and 24 months; 10 years | PTE in boys → positive correlation between heaviness of maternal smoking and conduct CD symptom disorder scores, only when mothers were unresponsive during infancy. | Wakschlag and Hans, 2002 |
Prospective cohort | 51/49 | 5, 10, and 16 years | PTE in both → dose-response relationship between prenatal exposure and childhood-onset conduct problems. | Maughan et al., 2001 |
Retrospective cohort | 52/48 | 2 years | PTE in both → related to negativity; negativity also related to a conflictual mother-child relationship. | Brook et al., 2000 |
Retrospective cohort | 48/52 | Time 1: 6–23 years; Time 2: 8–25 years; Time 310: 17–36 years of age | PTE in boys → increased risk of prepubertal conduct disorder onset. PTE in girls → increased risk of adolescent onset drug abuse/dependence. |
Weissman et al., 1999 |
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Preclinical
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Nicotine treatment | Rodent strain | Exposure period; test start | Finding | References |
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Vapour: 5 mg/ml; 1 h/d | Wistar rats | GD(−5)–GD20; PD22–PD37 | Nic males → increased anxiety-like behaviours (NSFT). | Lallai et al., 2022 |
Drinking water: 300 μg/ml Nic | NMRI mice | GD(−7)–PD1; PD42–PD49 | Nic males → increase in anxiety- and compulsive-like behaviours (EZM and MB). | Polli et al., 2020 |
Vapour: 16 mg/mL 3 h/d | CD-1 mice | GD0.5–GD17.5; ∼PD56 | PG/VG with Nic males → deficit in FST. | Church et al., 2020 |
Subcutaneous injections: 1.0 mg/kg; twice/d | Wistar rats | GD9–GD20; PD29–PD35 | Nic in females → increase in depressive-like behaviours (SP and OFT). | Zhang et al., 2019 |
Drinking water: 0.2 mg/ml Nic | C57BL/6J mice | GD0–GD13, GD14–PD0, GD0–PD0, GD14–PD7, GD0–PD7, or PD0–PD7; PD28–PD38 | Male Nic → increased anxiety-like behaviour in EPM for GD14–PD0, GD0–PD0, GD14–PD7, and GD0–PD7; MB for GD0–PD0, GD14–PD7, and GD0–PD0; NSFT for GD0–GD13, GD14–PD7, and GD0–PD0; Light/dark box test for GD0–PD0 and GD14–PD0. Female Nic → increased anxiety-like behaviour in EPM for GD0–PD0; MB for GD0–PD0 and GD14–PD0. |
Alkam et al., 2013a |
Osmotic minipump: 0.96 or 2.0 mg/kg/d | Long-Evans rats | GD4–PD10 (via maternal milk); PD32, PD72 | Nic males → increase in anxiety-like behaviours (EPM). | Eppolito et al., 2010 |
Osmotic minipump: 6 mg/kg/d | Sprague–Dawley rats | GD3–PD0; PD40 | Nic → increased anxiety-like behaviour in all groups except those exposed to saline and raised by natural mother; no effect of sex. | Vaglenova et al., 2004 |
Osmotic minipumps 2.5 or 5.0 mg/kg/d | Sprague–Dawley rats | GD8–GD20; 12–14 months | Females → higher consumption of sucrose and water; no effect of Nic treatment. Females in EPM → more entries into open and closed arms regardless of treatment. |
Sobrian et al., 2003 |
Osmotic minipump: 6 mg/kg/d | Zivic Miller Sprague–Dawley rats | GD12∼GD20; ∼3–5 months | Nic → elimination of pre-existing sex difference in saccharine preference. | Lichtensteiger and Schlumpf, 1985 |
Nic, Nicotine; Veh, vehicle; H, hour; D, day; W, week; GD, Gestation Day; PD, Postnatal Day; NSFT, Novelty Suppressed Feeding Test; EZM, Elevated Zero Maze; MB, Marble Burying; FST, Forced Swim Test; SP, Sucrose Preference; OFT, Open Field Test; EPM, Elevated Plus Maze.