Jun-Hong Dong1, Yi-Jing Wang1, Min Cui2, Xiao-Jing Wang3, Wen-Shuai Zheng2, Ming-Liang Ma1, Fan Yang4, Dong-Fang He5, Qiao-Xia Hu1, Dao-Lai Zhang5, Shang-Lei Ning6, Chun-Hua Liu2, Chuan Wang7, Yue Wang8, Xiang-Yao Li9, Fan Yi4, Amy Lin10, Alem W Kahsai10, Thomas Joseph Cahill10, Zhe-Yu Chen8, Xiao Yu1, Jin-Peng Sun11. 1. Key Laboratory Experimental Teratology of the Ministry of Education, Shandong University School of Medicine, China; Department of Biochemistry and Molecular Biology, Shandong University School of Medicine, China. 2. Physiology, Shandong University School of Medicine, China. 3. Cell Biology, Shandong University School of Medicine, China. 4. Key Laboratory Experimental Teratology of the Ministry of Education, Shandong University School of Medicine, China. 5. Key Laboratory Experimental Teratology of the Ministry of Education, Shandong University School of Medicine, China; Department of Biochemistry and Molecular Biology, Shandong University School of Medicine, China; Physiology, Shandong University School of Medicine, China. 6. Key Laboratory Experimental Teratology of the Ministry of Education, Shandong University School of Medicine, China; Department of Biochemistry and Molecular Biology, Shandong University School of Medicine, China; Qilu Hospital, Shandong University, Jinan, Shandong, China. 7. Department of Pharmacology, Hebei Medical University, Shijiazhuang, Hebei, China. 8. Neurobiology, Shandong University School of Medicine, China. 9. Zhejiang University, Institute of Neuroscience, China. 10. Duke University, School of Medicine, Durham, North Carolina. 11. Key Laboratory Experimental Teratology of the Ministry of Education, Shandong University School of Medicine, China; Department of Biochemistry and Molecular Biology, Shandong University School of Medicine, China; Duke University, School of Medicine, Durham, North Carolina. Electronic address: sunjinpeng@sdu.edu.cn.
Abstract
BACKGROUND: Stress is a conserved physiological response in mammals. Whereas moderate stress strengthens memory to improve reactions to previously experienced difficult situations, too much stress is harmful. METHODS: We used specific β-adrenergic agonists, as well as β2-adrenergic receptor (β2AR) and arrestin knockout models, to study the effects of adaptive β2AR activation on cognitive function using Morris water maze and object recognition experiments. We used molecular and cell biological approaches to elucidate the signaling subnetworks. RESULTS: We observed that the duration of the adaptive β2AR activation determines its consequences on learning and memory. Short-term formoterol treatment, for 3 to 5 days, improved cognitive function; however, prolonged β2AR activation, for more than 6 days, produced harmful effects. We identified the activation of several signaling networks downstream of β2AR, as well as an essential role for arrestin and lactate metabolism in promoting cognitive ability. Whereas Gs-protein kinase A-cyclic adenosine monophosphate response element binding protein signaling modulated monocarboxylate transporter 1 expression, β-arrestin-1 controlled expression levels of monocarboxylate transporter 4 and lactate dehydrogenase A through the formation of a β-arrestin-1/phospho-mitogen-activated protein kinase/hypoxia-inducible factor-1α ternary complex to upregulate lactate metabolism in astrocyte-derived U251 cells. Conversely, long-term treatment with formoterol led to the desensitization of β2ARs, which was responsible for its decreased beneficial effects. CONCLUSIONS: Our results not only revealed that β-arrestin-1 regulated lactate metabolism to contribute to β2AR functions in improved memory formation, but also indicated that the appropriate management of one specific stress pathway, such as through the clinical drug formoterol, may exert beneficial effects on cognitive abilities.
BACKGROUND:Stress is a conserved physiological response in mammals. Whereas moderate stress strengthens memory to improve reactions to previously experienced difficult situations, too much stress is harmful. METHODS: We used specific β-adrenergic agonists, as well as β2-adrenergic receptor (β2AR) and arrestin knockout models, to study the effects of adaptive β2AR activation on cognitive function using Morris water maze and object recognition experiments. We used molecular and cell biological approaches to elucidate the signaling subnetworks. RESULTS: We observed that the duration of the adaptive β2AR activation determines its consequences on learning and memory. Short-term formoterol treatment, for 3 to 5 days, improved cognitive function; however, prolonged β2AR activation, for more than 6 days, produced harmful effects. We identified the activation of several signaling networks downstream of β2AR, as well as an essential role for arrestin and lactate metabolism in promoting cognitive ability. Whereas Gs-protein kinase A-cyclic adenosine monophosphate response element binding protein signaling modulated monocarboxylate transporter 1 expression, β-arrestin-1 controlled expression levels of monocarboxylate transporter 4 and lactate dehydrogenase A through the formation of a β-arrestin-1/phospho-mitogen-activated protein kinase/hypoxia-inducible factor-1α ternary complex to upregulate lactate metabolism in astrocyte-derived U251 cells. Conversely, long-term treatment with formoterol led to the desensitization of β2ARs, which was responsible for its decreased beneficial effects. CONCLUSIONS: Our results not only revealed that β-arrestin-1 regulated lactate metabolism to contribute to β2AR functions in improved memory formation, but also indicated that the appropriate management of one specific stress pathway, such as through the clinical drug formoterol, may exert beneficial effects on cognitive abilities.
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