Key result
SAHA attenuates laparotomy-induced memory impairments in older mice by restoring hippocampal histone acetylation.
Why the study?
The role of histone acetylation in postoperative cognitive dysfunction (POCD) remains to be determined, especially in aged subjects.
Does suberoylanilide hydroxamic acid (SAHA) prevent postoperative cognitive dysfunction in aging mice?
Does suberoylanilide hydroxamic acid (SAHA) prevent postoperative cognitive dysfunction in aging mice?
p-value: p=0.049
SAHA, a histone deacetylase inhibitor, attenuates postoperative cognitive dysfunction and restores histone acetylation in aging mice.
Attenuates POCD in aged mice; hypothesis-generating for HDAC inhibition before any clinical translation.
Postoperative cognitive dysfunction (POCD) is a recognized clinical entity characterized with cognitive deficits after anesthesia and surgery, especially in aged patients. Previous studies have shown that histone acetylation plays a key role in hippocampal synaptic plasticity and memory formation. However, its role in POCD remains to be determined. Here, we show that suberoylanilide hydroxamic acid (SAHA), a histone deacetylase inhibitor, attenuates POCD in aging Mice. After exposed to the laparotomy, a surgical procedure involving an incision into abdominal walls to examine the abdominal organs, 16- but not 3-month old male C57BL/6 mice developed obvious cognitive impairments in the test of long-term contextual fear conditioning. Intracerebroventricular (i.c.v.) injection of SAHA at the dose of (20 μg/2 μl) 3 h before and daily after the laparotomy restored the laparotomy-induced reduction of hippocampal acetyl-H3 and acetyl-H4 levels and significantly attenuated the hippocampus-dependent long-term memory (LTM) impairments in 16-month old mice. SAHA also reduced the expression of cleaved caspase-3, inducible nitric oxide synthase (iNOS) and N-methyl-D-aspartate (NMDA) receptor-calcium/calmodulin dependent kinase II (CaMKII) pathway, and increased the expression of brain-derived neurotrophic factor (BDNF), synapsin 1, and postsynaptic density 95 (PSD95). Taken together, our data suggest that the decrease of histone acetylation contributes to POCD and may serve as a target to improve the neurological outcome of POCD.
No takes yet. Share an insight, caveat, or question.
Jia et al. (2015) studied Postoperative cognitive dysfunction (POCD) (n=128). Suberoylanilide hydroxamic acid (SAHA) vs. Vehicle (40% DMSO) was evaluated on Hippocampus-dependent long-term memory (LTM) evaluated by freezing time in contextual fear conditioning (p=0.049). Suberoylanilide hydroxamic acid (SAHA) significantly attenuated laparotomy-induced hippocampus-dependent long-term memory impairments and restored hippocampal histone acetylation levels in 16-month old mice.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: