Biometals. 2024 Jan 8. doi: 10.1007/s10534-023-00563-0. Online ahead of print.

ABSTRACT

There is limited experimental evidence on the biochemical consequences of aluminium (Al) and cadmium (Cd) co-exposures during pregnancy and postnatal life.This study investigated the impacts of perinatal Al chloride (AlCl₃) and Cd chloride (CdCl₂) co-exposures on neuroendocrine functions in mice offspring during postnatal life. The study comprised of four pregnant experimental groups. Group 1 received AlCl₃ (10 mg/kg), group 2 were administered CdCl₂ (1.5 mg/kg), while group 3 received both AlCl₃ (10 mg/kg) and CdCl₂ (1.5 mg/kg) (AlCl₃+CdCl₂), and group 4 received saline (10 mL/kg) only and served as control group. All experimental animals were chemically exposed once daily from gestation days 7-20. Upon delivery, male pups were regrouped based on maternal chemical exposure on postnatal day 21 (PND 21) and allowed to grow to adulthood until PND 78, after which they were sacrificed for assessment of neuroendocrine markers and histological investigations. There was no statistical significance (p > 0.05) on follicle stimulating hormone, testosterone, estrogen and progesterone, thyroid stimulating hormone, thyroxine (T4) in all treatment groups relative to controls|. However, AlCl₃ and AlCl₃-CdCl₂ significantly (p < 0.05) reduced triiodothyronine (T3) levels, with a profound increase in T3:T4 ratio by AlCl₃, and AlCl₃+CdCl₂ compared to control. Furthermore, pups from pregnant mice treated with CdCl₂ and AlCl₃+CdCl₂ demonstrated increased testicular malondialdehyde concentration with increased catalase activity relative to controls, suggesting oxidative imbalance. In addition, AlCl₃, CdCl₂, and AlCl₃+CdCl₂ exposures induced testicular and hypothalamic architectural disruption compared to controls, with marked architectural derangement in the AlCl₃+CdCl₂ group. Our findings suggest that prenatal co-exposures to Alcl₃ and CdCl₂ induce testicular and hypothalamic alterations in offspring via a testicular oxidative stress and thyrotoxicosis-dependent mechanisms.

PMID:38190032 | DOI:10.1007/s10534-023-00563-0