Age-related neuroinflammation and pathology in the locus coeruleus and hippocampus: beta-adrenergic antagonists exacerbate impairment of learning and memory in aged mice

被引:19
作者
Evans, Andrew K. [1 ,2 ]
Park, Heui Hye [2 ]
Saw, Nay Lui [2 ]
Singhal, Kratika [3 ]
Ogawa, Gaku [2 ]
Leib, Ryan D. [3 ]
Shamloo, Mehrdad [1 ,2 ]
机构
[1] Stanford Univ, Dept Neurosurg, Sch Med, 1050 Arastradero Rd,Bldg A, Palo Alto, CA 94304 USA
[2] Stanford Univ, Wu Tsai Neurosci Inst, Stanford Behav & Funct Neurosci Lab, Stanford, CA 94304 USA
[3] Stanford Univ, Vincent Coates Fdn Mass Spectrometry Lab, Stanford, CA 94304 USA
基金
美国国家卫生研究院;
关键词
Locus coeruleus; Beta-blocker; Aging; proteomics; Inflammation; Behavior; COGNITIVE IMPAIRMENT; NERVOUS-SYSTEM; NMDA RECEPTOR; PROTEIN; MODEL; DEGENERATION; EXPRESSION; KINASE;
D O I
10.1016/j.neurobiolaging.2021.06.012
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
The locus coeruleus (LC) provides the primary noradrenergic input to the forebrain and hippocampus, and may be vulnerable to degeneration and contribute to age-related cognitive decline and neuroinflammation. Additionally, inhibition of noradrenergic transmission by brain-permeable beta-blockers could exacerbate cognitive impairment. This study examined effects of age and acute beta-blocker administration on LC and hippocampus pathology, neuroinflammation and learning and memory behavior in mice. Male mice, 3 and 18 months old, were administered propranolol (beta-blocker) or mabuterol (beta-adrenergic agonist) acutely around behavioral assessment. Terminal inflammatory markers in plasma, hippocampus and LC were assessed alongside histopathology. An increase in hippocampal and LC microgliosis and inflammatory proteins in the hippocampus was detected in aged mice. We report pathological hyperphosphorylation of the postsynaptic NMDA receptor subunit 2B (NR2B) in the hippocampus, suggesting neuronal hyperexcitability. Furthermore, the aged proteome revealed an induction in proteins related to energy metabolism, and mitochondria dysfunction in the LC and hippocampus. In a series of hippocampal dependent behavioral assessment tasks acute beta-adrenergic agonist or beta blocker administration altered learning and memory behavior in both aged and young mice. In Y-maze, propranolol and mabuterol differentially altered time spent in novel versus familiar arms in young and aged mice. Propranolol impaired Novel Object Recognition in both young and aged mice. Mabuterol enhanced trace learning in fear conditioning. Aged mice froze more to context and less to cue. Propranolol impaired contextual recall in aged mice. Concluding, aged mice show LC and hippocampus pathology and heightened effects of betaadrenergic pharmacology on learning and memory. (c) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:241 / 256
页数:16
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