The associations between prenatal plastic phthalate exposure and lipid acylcarnitine levels in humans and mice

被引:0
|
作者
Vacy, Kristina [1 ,2 ]
Rupasinghe, Thusi [3 ]
Bjorksten, Alicia [1 ]
Gogos, Andrea [1 ]
Meikle, Peter J. [4 ,5 ]
Burugupalli, Satvika [5 ]
Boon, Wah Chin [1 ]
Ponsonby, Anne-Louise [1 ,6 ,7 ]
机构
[1] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville 3010, Australia
[2] Univ Melbourne, Melbourne Sch Populat & Global Hlth, Parkville 3010, Australia
[3] SCIEX Ltd, Mulgrave 3170, Australia
[4] Baker Heart & Diabet Inst, Metabol Lab, Melbourne 3004, Australia
[5] La Trobe Univ, Baker Dept Cardiovasc Res Translat & Implementat, Bundoora 3086, Australia
[6] Royal Childrens Hosp, Murdoch Childrens Res Inst, Parkville 3010, Australia
[7] Univ Melbourne, Dept Paediat, Parkville 3010, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Lipidomics; Acylcarnitine; Phthalates; Endocrine disruptors; Plasticizers; CARNITINE PALMITOYLTRANSFERASE; DEHP; OXIDATION; OBESITY; FEMALE; LIVER; RAT; BIOCHEMISTRY; METABOLOME; ACTIVATION;
D O I
10.1016/j.reprotox.2025.108835
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Phthalates are ubiquitous environmental pollutants known for their endocrine-disrupting properties, particularly during critical periods such as pregnancy and early childhood. Phthalates alter lipid metabolism, but the role of prenatal exposure on the offspring lipidome is less understood. In particular, we focused on long chain acylcarnitines- intermediates of fatty acid oxidation that serve as potential biomarkers of mitochondrial function and energy metabolism. This study aimed (i) to investigate the association between prenatal phthalate exposure and the child's blood acylcarnitine concentrations and, (ii) to evaluate the impact of prenatal administration of di-(2ethylhexyl) phthalate (DEHP) on acylcarnitine levels in mouse offspring blood, brain and liver. We conducted analyses of both a prospective birth cohort study and an experimental study in mice. From the Barwon Infant Study cohort (1074 mother-child pairs), prenatal phthalate exposure was assessed at 36 weeks' gestation and its association with acylcarnitine levels was examined in cord blood, and child's blood at 6 months, 12 months and 4 years. In mice, pregnant C57BL/6 J mouse dams were exposed to 20 mu g/kg DEHP for 5 days mid-gestation, and offspring tissues were analyzed at 1 month of age postnatally for acylcarnitine profiles. Our findings demonstrate that prenatal phthalate levels (specifically butyl benzyl phthalate (BBzP) and diisobutyl phthalate (DiBP)) are inversely associated with total long chain acylcarnitine levels in human cord blood at birth. In contrast, BBzP was positively associated with the long chain acylcarnitines at 12 months of age. In mice, prenatal DEHP exposure for only 5 days led to decreased palmitoylcarnitine (AC16:0) levels in the brain and liver, but not in blood. Taken together, our findings highlight that prenatal phthalate exposure can alter acylcarnitine profiles, indicating disruptions in fatty acid metabolism that may have long-term effects on metabolic health.
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页数:11
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