Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, UT 84108, USA.
Department of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT 84108, USA.
Int J Mol Sci. 2022 Aug 4;23(15):8654. doi: 10.3390/ijms23158654.
Classic Galactosemia (CG) is a devastating inborn error of the metabolism caused by mutations in the GALT gene encoding the enzyme galactose-1 phosphate uridylyltransferase in galactose metabolism. Severe complications of CG include neurological impairments, growth restriction, cognitive delays, and, for most females, primary ovarian insufficiency. The absence of the GALT enzyme leads to an accumulation of aberrant galactose metabolites, which are assumed to be responsible for the sequelae. There is no treatment besides the restriction of dietary galactose, which does not halt the development of the complications; thus, additional treatments are sorely needed. Supplements have been used in other inborn errors of metabolism but are not part of the therapeutic regimen for CG. The goal of this study was to test two generally recognized as safe supplements (purple sweet potato color (PSPC) and -inositol (MI)) that may impact cellular pathways contributing to the complications in CG. Our group uses a gene-trapped mouse model to study the pathophysiology in CG, which phenocopy many of the complications. Here we report the ability of PSPC to ameliorate dysregulation in the ovary, brain, and liver of our mutant mice as well as positive results of MI supplementation in the ovary and brain.
经典半乳糖血症(CG)是一种由半乳糖代谢中 GALT 基因编码的酶半乳糖-1-磷酸尿苷酰转移酶突变引起的破坏性先天性代谢错误。CG 的严重并发症包括神经损伤、生长受限、认知延迟,以及大多数女性的原发性卵巢功能不全。GALT 酶的缺失导致异常半乳糖代谢物的积累,这些代谢物被认为是导致后遗症的原因。除了限制饮食中的半乳糖之外,没有其他治疗方法,而这种方法并不能阻止并发症的发展;因此,非常需要额外的治疗方法。补充剂已被用于其他先天性代谢错误,但不属于 CG 的治疗方案。本研究的目的是测试两种被普遍认为安全的补充剂(紫甘薯色素(PSPC)和肌醇(MI)),它们可能影响导致 CG 并发症的细胞途径。我们的小组使用基因捕获小鼠模型来研究 CG 的病理生理学,该模型模拟了许多并发症。在这里,我们报告了 PSPC 改善我们突变小鼠的卵巢、大脑和肝脏中失调的能力,以及 MI 补充剂在卵巢和大脑中的积极结果。