Effects of food-borne docosahexaenoic acid supplementation on bone lead mobilisation, mitochondrial function and serum metabolomics in pre-pregnancy lead-exposed lactating rats

• Published in: Environmental pollution (1987) 2023-11, Vol.337, p.122613-122613, Article 122613
• Main Authors: Lu, An-Xin, Lin, Yin, Li, Jing, Liu, Jun-Xia, Yan, Chong-Huai, Zhang, Lin
• Format: Article
• Language: English
• Subjects: Bone Pb mobilisation; DHA; Lead; Metabolomics; Mitochondrial dysfunction
• ISSN: 0269-7491; 1873-6424
• DOI: 10.1016/j.envpol.2023.122613

Large bone lead (Pb) resulting from high environmental exposure during childhood is an important source of endogenous Pb during pregnancy and lactation. Docosahexaenoic acid (DHA) attenuates Pb toxicity, however, the effect of DHA on bone Pb mobilisation during lactation has not been investigated. We aimed to study the effects of DHA supplementation during pregnancy and lactation on bone Pb mobilisation during lactation and its potential mechanisms. Weaning female rats were randomly divided into control (0.05% sodium acetate) and Pb-exposed (0.05% Pb acetate) groups, after a 4-week exposure by ad libitum drinking and a subsequent 4-week washout period, all female rats were mated with healthy males until pregnancy. Then exposed rats were randomly divided into Pb and Pb + DHA groups, and the latter was given a 0.14% DHA diet, while the remaining groups were given normal feed until the end of lactation. Pb and calcium levels, bone microarchitecture, bone turnover markers, mitochondrial function and serum metabolomics were analyzed. The results showed that higher blood and bone Pb levels were observed in the Pb group compared to the control, and there was a significant negative correlation between blood and bone Pb. Also, Pb increased trabecular bone loss along with slightly elevated serum C-telopeptide of type I collagen (CTX-I) levels. However, DHA reduced CTX-I levels and improved trabecular bone microarchitecture. Metabolomics showed that Pb affected mitochondrial function, which was further demonstrated in bone tissue by significant reductions in ATP levels, Na+-K+-ATPase, Ca2+-Mg2+-ATPase and CAT activities, and elevated levels of MDA, IL-1β and IL-18. However, these alterations were partially mitigated by DHA. In conclusion, DHA supplementation during pregnancy and lactation improved bone Pb mobilisation and mitochondrial dysfunction in lactating rats induced by pre-pregnancy Pb exposure, providing potential means of mitigating bone Pb mobilisation levels during lactation, but the mechanism still needs further study. [Display omitted] •Pre-pregnancy Pb exposure enhanced bone Pb mobilisation in lactating rats.•Pb abnormally altered bone microarchitecture and mitochondrial function.•DHA supplementation attenuated bone disruptions and mitochondrial dysfunction.•Pb affected metabolites involving energetic, oxidative and inflammatory pathways.•Lactating women who were exposed to Pb may benefit from DHA.