Abnormal Porphyrin Metabolism in Autism Spectrum Disorder and Therapeutic Implications

被引:1
作者
Indika, Neluwa-Liyanage R. [1 ]
Senarathne, Udara D. [1 ,2 ]
Malvaso, Antonio [3 ]
Darshana, Dhanushka [4 ]
Owens, Susan C. [5 ]
Mansouri, Borhan [6 ]
Semenova, Yuliya [7 ]
Bjorklund, Geir [8 ]
机构
[1] Univ Sri Jayewardenepura, Fac Med Sci, Dept Biochem, Nugegoda 10250, Sri Lanka
[2] Monash Hlth, Dept Chem Pathol, Monash Hlth Pathol, Clayton, Vic, Australia
[3] Univ Pavia, IRCCS C Mondino Fdn, Natl Neurol Inst, Dept Brain & Behav Sci, Pavia, Italy
[4] Univ Ruhuna, Fac Allied Hlth Sci, Dept Pharm, Galle, Sri Lanka
[5] Autism Res Inst, Autism Oxalate Project, San Diego, CA USA
[6] Kermanshah Univ Med Sci, Res Inst Hlth, Subst Abuse Prevent Res Ctr, Kermanshah, Iran
[7] Nazarbayev Univ, Sch Med, Astana, Kazakhstan
[8] Council Nutr & Environm Med, Toften 24, N-8610 Mo I Rana, Norway
关键词
Autism; Porphyrin; Mercury; Lead; Heavy metal; Chelator; Thiol; ENVIRONMENTAL MERCURY RELEASE; URINARY PORPHYRINS; COPROPORPHYRINOGEN OXIDASE; TOXICITY BIOMARKERS; COMPLEX-FORMATION; MITOCHONDRIAL DYSFUNCTION; OXIDATIVE STRESS; KIDNEY MERCURY; CHILDREN; LEAD;
D O I
10.1007/s12035-023-03722-z
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Autism spectrum disorder (ASD) is a mosaic of neurodevelopmental conditions composed of early-onset social interaction and communication deficits, along with repetitive and/or restricted patterns of activities, behavior, and interests. ASD affects around 1% of children worldwide, with a male predominance. Energy, porphyrin, and neurotransmitter homeostasis are the key metabolic pathways affected by heavy metal exposure, potentially implicated in the pathogenesis of ASD. Exposure to heavy metals can lead to an altered porphyrin metabolism due to enzyme inhibition by heavy metals. Heavy metal exposure, inborn genetic susceptibility, and abnormal thiol and selenol metabolism may play a significant role in the urinary porphyrin profile anomalies observed in ASD. Altered porphyrin metabolism in ASD may also be associated with, vitamin B6 deficiency, hyperoxalemia, hyperhomocysteinemia, and hypomagnesemia. The present review considers the abnormal porphyrin metabolism in ASD in relation to the potential pathogenic mechanism and discusses the possible metabolic therapies such as vitamins, minerals, cofactors, and antioxidants that need to be explored in future research. Such targeted therapeutic therapies would bring about favorable outcomes such as improvements in core and co-occurring symptoms.
引用
收藏
页码:3851 / 3866
页数:16
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