Hydrogen sulfide slows down progression of experimental Alzheimer's disease by targeting multiple pathophysiological mechanisms

被引:225
作者
Giuliani, Daniela [1 ]
Ottani, Alessandra [1 ]
Zaffe, Davide [2 ]
Galantucci, Maria [1 ]
Strinati, Flavio [3 ]
Lodi, Renzo [4 ]
Guarini, Salvatore [1 ]
机构
[1] Univ Modena & Reggio Emilia, Sect Pharmacol & Mol Med, Dept Biomed Metab & Neural Sci, I-41125 Modena, Italy
[2] Univ Modena & Reggio Emilia, Sect Human Morphol, Dept Biomed Metab & Neural Sci, I-41125 Modena, Italy
[3] Tabianos Spa, Tabiano, Italy
[4] Univ Modena & Reggio Emilia, Dept Gen Surg & Surg Specialties, I-41125 Modena, Italy
关键词
Alzheimer's disease; Pathophysiological pathways; Learning and memory; Hydrogen sulfide; Spa-waters; Neuroprotection; TRAUMATIC BRAIN-INJURY; NEURODEGENERATIVE DISEASES; CEREBRAL-ISCHEMIA; RAT MODEL; SYNAPTIC DYSFUNCTION; COGNITIVE DEFICITS; DELAYED TREATMENT; MOUSE MODEL; MELANOCORTINS; NEUROPROTECTION;
D O I
10.1016/j.nlm.2013.05.006
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
010107 [宗教学]; 030301 [社会学]; 070906 [古生物学及地层学(含古人类学)];
摘要
It has been previously reported that brain hydrogen sulfide (H2S) synthesis is severely decreased in Alzheimer's disease (AD) patients, and plasma H2S levels are negatively correlated with the severity of AD. Here we extensively investigated whether treatment with a H2S donor and spa-waters rich in H2S induces neuroprotection and slows down progression of AD. Studies with sodium hydrosulfide (a H2S donor) and Tabiano's spa-water were carried out in three experimental models of AD. Short-term and long-term treatments with sodium hydrosulfide and/or Tabiano's spa-water significantly protected against impairment in learning and memory in rat models of AD induced by brain injection of beta-amyloid(1-40) (A beta) or streptozotocin, and in an AD mouse model harboring human transgenes APP(Swe), PS1(M146V) and tau(P301L) (3xTg-AD mice). The improvement in behavioral performance was associated with hippocampus was size of A beta plaques and preservation of the morphological picture, as found in AD rats. Further, lowered concentration/phosphorylation levels of proteins thought to be the central events in AD pathophysiology, namely amyloid precursor protein, presenilin-1, A beta(1-42) and tau phosphorylated at Thr181, Ser396 and Ser202, were detected in 3xTg-AD mice treated with spa-water. The excitotoxicity-triggered oxidative and nitrosative stress was counteracted in 3xTg-AD mice, as indicated by the decreased levels of malondialdehyde and nitrites in the cerebral cortex. Hippocampus reduced activity of c-jun N-terminal kinases, extracellular signal-regulated kinases and p38, which have an established role not only in phosphorylation of tau protein but also in inflammation and apoptosis, was also found. Consistently, decrease in tumor necrosis factor-alpha level, up-regulation of Bcl-2, and down-regulation of BAX and the downstream executioner caspase-3, also occurred in the hippocampus of 3xTg-AD mice after treatment with Tabiano's spa-water, thus suggesting that it is also able to modulate inflammation and apoptosis. Our findings indicate that appropriate treatments with H2S donors and Tabiano's spa-waters, and may be other spa-waters rich in H2S content, might represent an innovative approach to slow down AD progression in humans by targeting multiple pathophysiological mechanisms. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:82 / 91
页数:10
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