MMP-9-BDNF pathway is implicated in cognitive impairment of male individuals with methamphetamine addiction during early withdrawal
•Of methamphetamine (METH) early abstainers, 61.18% exhibit cognitive impairment.•Early withdrawal from METH decreases mBDNF, proBDNF expression and M/P ratio.•MMP-9-BDNF pathway is implicated in cognitive impairment of early METH abstainers.•Combined of mBDNF, TrkB, MMP-9, MMP-9 activity predict co...
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Published in | Behavioural brain research Vol. 366; pp. 29 - 35 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
02.07.2019
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ISSN | 0166-4328 1872-7549 1872-7549 |
DOI | 10.1016/j.bbr.2019.03.020 |
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Abstract | •Of methamphetamine (METH) early abstainers, 61.18% exhibit cognitive impairment.•Early withdrawal from METH decreases mBDNF, proBDNF expression and M/P ratio.•MMP-9-BDNF pathway is implicated in cognitive impairment of early METH abstainers.•Combined of mBDNF, TrkB, MMP-9, MMP-9 activity predict cognitive impairment of METH abstainers.
Cognitive impairment is often concomitant with current and abstinent methamphetamine (METH) misuse. However, the mechanism underlying the pathogenesis of cognitive impairment induced by METH remains unclear. As evidence indicates that brain-derived neurotrophic factor (BDNF) is associated with METH addiction, the present study aimed to investigate whether BDNF and the proteins regulating the BDNF signaling pathway might be implicated in the cognitive impairment of the METH abusers during early withdrawal. A total of 171 male subjects were recruited, including 85 METH abstainers and 86 healthy controls. Cognitive function was evaluated with the Montreal Cognitive Assessment (MoCA) screening tool. The levels of serum proteins that regulate the BDNF signaling pathway were measured using enzyme-linked immunosorbent assay kits. 61.18% METH abstainers were determined to have cognitive impairment (MoCA<26). The serum levels of mBDNF, proBDNF, and MMP-9, as well as the ratio of the mBDNF/proBDNF (M/P) were significantly decreased in the cognition-impaired METH abstainers than in the cognition-unimpaired METH abstainers. mBDNF, proBDNF, TrkB, MMP-9, MMP-9 activity, and M/P were significantly correlated with the MoCA score in the METH abstainers. The combination of mBDNF, TrkB, MMP-9, and MMP-9 activity demonstrated excellent diagnostic potential for cognitive impairment of METH abusers during early withdrawal (AUC = 0.978). The results provide the prospective evidence that the MMP-9-BDNF pathway may underlie the pathogenesis of cognitive impairment in METH abusers during early withdrawal. |
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AbstractList | Cognitive impairment is often concomitant with current and abstinent methamphetamine (METH) misuse. However, the mechanism underlying the pathogenesis of cognitive impairment induced by METH remains unclear. As evidence indicates that brain-derived neurotrophic factor (BDNF) is associated with METH addiction, the present study aimed to investigate whether BDNF and the proteins regulating the BDNF signaling pathway might be implicated in the cognitive impairment of the METH abusers during early withdrawal. A total of 171 male subjects were recruited, including 85 METH abstainers and 86 healthy controls. Cognitive function was evaluated with the Montreal Cognitive Assessment (MoCA) screening tool. The levels of serum proteins that regulate the BDNF signaling pathway were measured using enzyme-linked immunosorbent assay kits. 61.18% METH abstainers were determined to have cognitive impairment (MoCA<26). The serum levels of mBDNF, proBDNF, and MMP-9, as well as the ratio of the mBDNF/proBDNF (M/P) were significantly decreased in the cognition-impaired METH abstainers than in the cognition-unimpaired METH abstainers. mBDNF, proBDNF, TrkB, MMP-9, MMP-9 activity, and M/P were significantly correlated with the MoCA score in the METH abstainers. The combination of mBDNF, TrkB, MMP-9, and MMP-9 activity demonstrated excellent diagnostic potential for cognitive impairment of METH abusers during early withdrawal (AUC = 0.978). The results provide the prospective evidence that the MMP-9-BDNF pathway may underlie the pathogenesis of cognitive impairment in METH abusers during early withdrawal. Cognitive impairment is often concomitant with current and abstinent methamphetamine (METH) misuse. However, the mechanism underlying the pathogenesis of cognitive impairment induced by METH remains unclear. As evidence indicates that brain-derived neurotrophic factor (BDNF) is associated with METH addiction, the present study aimed to investigate whether BDNF and the proteins regulating the BDNF signaling pathway might be implicated in the cognitive impairment of the METH abusers during early withdrawal. A total of 171 male subjects were recruited, including 85 METH abstainers and 86 healthy controls. Cognitive function was evaluated with the Montreal Cognitive Assessment (MoCA) screening tool. The levels of serum proteins that regulate the BDNF signaling pathway were measured using enzyme-linked immunosorbent assay kits. 61.18% METH abstainers were determined to have cognitive impairment (MoCA<26). The serum levels of mBDNF, proBDNF, and MMP-9, as well as the ratio of the mBDNF/proBDNF (M/P) were significantly decreased in the cognition-impaired METH abstainers than in the cognition-unimpaired METH abstainers. mBDNF, proBDNF, TrkB, MMP-9, MMP-9 activity, and M/P were significantly correlated with the MoCA score in the METH abstainers. The combination of mBDNF, TrkB, MMP-9, and MMP-9 activity demonstrated excellent diagnostic potential for cognitive impairment of METH abusers during early withdrawal (AUC = 0.978). The results provide the prospective evidence that the MMP-9-BDNF pathway may underlie the pathogenesis of cognitive impairment in METH abusers during early withdrawal.Cognitive impairment is often concomitant with current and abstinent methamphetamine (METH) misuse. However, the mechanism underlying the pathogenesis of cognitive impairment induced by METH remains unclear. As evidence indicates that brain-derived neurotrophic factor (BDNF) is associated with METH addiction, the present study aimed to investigate whether BDNF and the proteins regulating the BDNF signaling pathway might be implicated in the cognitive impairment of the METH abusers during early withdrawal. A total of 171 male subjects were recruited, including 85 METH abstainers and 86 healthy controls. Cognitive function was evaluated with the Montreal Cognitive Assessment (MoCA) screening tool. The levels of serum proteins that regulate the BDNF signaling pathway were measured using enzyme-linked immunosorbent assay kits. 61.18% METH abstainers were determined to have cognitive impairment (MoCA<26). The serum levels of mBDNF, proBDNF, and MMP-9, as well as the ratio of the mBDNF/proBDNF (M/P) were significantly decreased in the cognition-impaired METH abstainers than in the cognition-unimpaired METH abstainers. mBDNF, proBDNF, TrkB, MMP-9, MMP-9 activity, and M/P were significantly correlated with the MoCA score in the METH abstainers. The combination of mBDNF, TrkB, MMP-9, and MMP-9 activity demonstrated excellent diagnostic potential for cognitive impairment of METH abusers during early withdrawal (AUC = 0.978). The results provide the prospective evidence that the MMP-9-BDNF pathway may underlie the pathogenesis of cognitive impairment in METH abusers during early withdrawal. •Of methamphetamine (METH) early abstainers, 61.18% exhibit cognitive impairment.•Early withdrawal from METH decreases mBDNF, proBDNF expression and M/P ratio.•MMP-9-BDNF pathway is implicated in cognitive impairment of early METH abstainers.•Combined of mBDNF, TrkB, MMP-9, MMP-9 activity predict cognitive impairment of METH abstainers. Cognitive impairment is often concomitant with current and abstinent methamphetamine (METH) misuse. However, the mechanism underlying the pathogenesis of cognitive impairment induced by METH remains unclear. As evidence indicates that brain-derived neurotrophic factor (BDNF) is associated with METH addiction, the present study aimed to investigate whether BDNF and the proteins regulating the BDNF signaling pathway might be implicated in the cognitive impairment of the METH abusers during early withdrawal. A total of 171 male subjects were recruited, including 85 METH abstainers and 86 healthy controls. Cognitive function was evaluated with the Montreal Cognitive Assessment (MoCA) screening tool. The levels of serum proteins that regulate the BDNF signaling pathway were measured using enzyme-linked immunosorbent assay kits. 61.18% METH abstainers were determined to have cognitive impairment (MoCA<26). The serum levels of mBDNF, proBDNF, and MMP-9, as well as the ratio of the mBDNF/proBDNF (M/P) were significantly decreased in the cognition-impaired METH abstainers than in the cognition-unimpaired METH abstainers. mBDNF, proBDNF, TrkB, MMP-9, MMP-9 activity, and M/P were significantly correlated with the MoCA score in the METH abstainers. The combination of mBDNF, TrkB, MMP-9, and MMP-9 activity demonstrated excellent diagnostic potential for cognitive impairment of METH abusers during early withdrawal (AUC = 0.978). The results provide the prospective evidence that the MMP-9-BDNF pathway may underlie the pathogenesis of cognitive impairment in METH abusers during early withdrawal. |
Author | Wu, Yulong Ma, Lin Liu, Qiang Jing, Pengcheng Jiao, Shaoli Cheng, Mei Hao, Yuling Pan, Chenmin Wang, Yan |
Author_xml | – sequence: 1 givenname: Mei surname: Cheng fullname: Cheng, Mei email: chm790217@126.com organization: Institute of Health and Disease Management, Binzhou Medical University, Guanhai Road 346, 264003, Yantai, China – sequence: 2 givenname: Qiang surname: Liu fullname: Liu, Qiang organization: Affiliated Hospital of Binzhou Medical University, Huanghe Road 661, 256603, Binzhou, China – sequence: 3 givenname: Yan surname: Wang fullname: Wang, Yan organization: Institute of Health and Disease Management, Binzhou Medical University, Guanhai Road 346, 264003, Yantai, China – sequence: 4 givenname: Yuling surname: Hao fullname: Hao, Yuling organization: Institute of Health and Disease Management, Binzhou Medical University, Guanhai Road 346, 264003, Yantai, China – sequence: 5 givenname: Pengcheng surname: Jing fullname: Jing, Pengcheng organization: Yantai Drug Addiction Treatment Center, Tongshi south Road 222, 264003, Yantai, China – sequence: 6 givenname: Shaoli surname: Jiao fullname: Jiao, Shaoli organization: Yantai Drug Addiction Treatment Center, Tongshi south Road 222, 264003, Yantai, China – sequence: 7 givenname: Lin surname: Ma fullname: Ma, Lin organization: Yantai Drug Addiction Treatment Center, Tongshi south Road 222, 264003, Yantai, China – sequence: 8 givenname: Chenmin surname: Pan fullname: Pan, Chenmin organization: Yantai Drug Addiction Treatment Center, Tongshi south Road 222, 264003, Yantai, China – sequence: 9 givenname: Yulong surname: Wu fullname: Wu, Yulong email: ylongwu@126.com organization: Department of Pathogenic Biology, Binzhou Medical University, Guanhai Road 346, 264003, Yantai, China |
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Keywords | Male Methamphetamine addiction Withdrawal BDNF MMP-9 Cognitive impairment |
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Snippet | •Of methamphetamine (METH) early abstainers, 61.18% exhibit cognitive impairment.•Early withdrawal from METH decreases mBDNF, proBDNF expression and M/P... Cognitive impairment is often concomitant with current and abstinent methamphetamine (METH) misuse. However, the mechanism underlying the pathogenesis of... |
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SubjectTerms | Adult Amphetamine-Related Disorders - metabolism BDNF Behavior, Addictive - metabolism Brain-Derived Neurotrophic Factor - metabolism Brain-Derived Neurotrophic Factor - physiology Cognitive Dysfunction - metabolism Cognitive Dysfunction - psychology Cognitive impairment Drug Users - psychology Humans Male Matrix Metalloproteinase 9 - metabolism Matrix Metalloproteinase 9 - physiology Methamphetamine - adverse effects Methamphetamine - metabolism Methamphetamine addiction Middle Aged MMP-9 Substance Withdrawal Syndrome - metabolism Substance-Related Disorders - metabolism Withdrawal |
Title | MMP-9-BDNF pathway is implicated in cognitive impairment of male individuals with methamphetamine addiction during early withdrawal |
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