共 95 条
Opiate Analgesics as Negative Modulators of Adult Hippocampal Neurogenesis: Potential Implications in Clinical Practice
被引:22
作者:

Bortolotto, Valeria
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机构:
Univ Piemonte Orientale, Dept Pharmaceut Sci, Lab Neuroplast, Novara, Italy Univ Piemonte Orientale, Dept Pharmaceut Sci, Lab Neuroplast, Novara, Italy

Grilli, Mariagrazia
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h-index: 0
机构:
Univ Piemonte Orientale, Dept Pharmaceut Sci, Lab Neuroplast, Novara, Italy Univ Piemonte Orientale, Dept Pharmaceut Sci, Lab Neuroplast, Novara, Italy
机构:
[1] Univ Piemonte Orientale, Dept Pharmaceut Sci, Lab Neuroplast, Novara, Italy
来源:
FRONTIERS IN PHARMACOLOGY
|
2017年
/
8卷
关键词:
opiates;
morphine;
methadone;
tapentadol;
neural stem cells;
adult neurogenesis;
chronic pain;
depression;
CHRONIC RESTRAINT STRESS;
NEURAL PROGENITOR CELLS;
NONCANCER PAIN PATIENTS;
RAT DENTATE GYRUS;
SUBGRANULAR ZONE;
PROLIFERATING CELLS;
MAJOR DEPRESSION;
NEUROPATHIC PAIN;
NMDA RECEPTOR;
SHORT-TERM;
D O I:
10.3389/fphar.2017.00254
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
During the past decade, studies of the mechanisms and functional implications of adult hippocampal neurogenesis (ahNG) have significantly progressed. At present, it is proposed that adult born neurons may contribute to a variety of hippocampal-related functions, including specific cognitive aspects and mood regulation. Several groups focussed on the factors that regulate proliferation and fate determination of adult neural stem/progenitor cells (NSC/NPC), including clinically relevant drugs. Opiates were the first drugs shown to negatively impact neurogenesis in the adult mammalian hippocampus. Since that initial report, a vast array of information has been collected on the effect of opiate drugs, by either modulating proliferation of stem/progenitor cells or interfering with differentiation, maturation and survival of adult born neurons. The goal of this review is to critically revise the present state of knowledge on the effect of opiate drugs on the different developmental stages of ahNG, as well as the possible underlying mechanisms. We will also highlight the potential impact of deregulated hippocampal neurogenesis on patients undergoing chronic opiate treatment. Finally, we will discuss the differences in the negative impact on ahNG among clinically relevant opiate drugs, an aspect that may be potentially taken into account to avoid long-term deregulation of neural plasticity and its associated functions in the clinical practice.
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