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Int J Neuropsychopharmacol. 2017 Apr 1;20(4):305-315. doi: 10.1093/ijnp/pyw103.

Hydrogen Sulfide Ameliorates Homocysteine-Induced Cognitive Dysfunction by Inhibition of Reactive Aldehydes Involving Upregulation of ALDH2.

Li M1, Zhang P1, Wei HJ2,3, Li MH1, Zou W1, Li X4, Gu HF2, Tang XQ1,2,3.

Author information

1
Department of Neurology, Nanhua Affiliated Hospital.
2
Institute of Neuroscience, Medical College.
3
University of South China, Hengyang, Hunan, PR China; Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, Hengyang, Hunan, PR China.
4
Department of Anesthesiology, First Affiliated Hospital, University of South China, Hengyang, Hunan, PR China.

Abstract

Background:

Homocysteine, a risk factor for Alzheimer's disease, induces cognitive dysfunction. Reactive aldehydes play an important role in cognitive dysfunction. Aldehyde-dehydrogenase 2 detoxifies reactive aldehydes. Hydrogen sulfide, a novel neuromodulator, has neuroprotective effects and regulates learning and memory. Our previous work confirmed that the disturbance of hydrogen sulfide synthesis is invovled in homocysteine-induced defects in learning and memory. Therefore, the present work was to explore whether hydrogen sulfide ameliorates homocysteine-generated cognitive dysfunction and to investigate whether its underlying mechanism is related to attenuating accumulation of reactive aldehydes by upregulation of aldehyde-dehydrogenase 2.

Methods:

The cognitive function of rats was assessed by the Morris water maze test and the novel object recognition test. The levels of malondialdehyde, 4-hydroxynonenal, and glutathione as well as the activity of aldehyde-dehydrogenase 2 were determined by enzyme linked immunosorbent assay; the expression of aldehyde-dehydrogenase 2 was detected by western blot.

Results:

The behavior experiments, Morris water maze test and novel objects recognition test, showed that homocysteine induced deficiency in learning and memory in rats, and this deficiency was reversed by treatment of NaHS (a donor of hydrogen sulfide). We demonstrated that NaHS inhibited homocysteine-induced increases in generations of MDA and 4-HNE in the hippocampus of rats and that hydrogen sulfide reversed homocysteine-induced decreases in the level of glutathione as well as the activity and expression of aldehyde-dehydrogenase 2 in the hippocampus of rats.

Conclusion:

Hydrogen sulfide ameliorates homocysteine-induced impairment in cognitive function by decreasing accumulation of reactive aldehydes as a result of upregulations of glutathione and aldehyde-dehydrogenase 2.

KEYWORDS:

ALDH2; GSH; cognitive dysfunction; homocysteine; hydrogen sulfide; reactive aldehydes

PMID:
27988490
PMCID:
PMC5409037
DOI:
10.1093/ijnp/pyw103
[Indexed for MEDLINE]
Free PMC Article

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