Modulatory role of neurosteroidogenesis in the spinal cord during peripheral nerve injury-induced chronic pain

被引:1
|
作者
Mensah-Nyagan, Ayikoe-Guy [1 ]
Meyer, Laurence [1 ]
Patte-Mensah, Christine [1 ]
机构
[1] Univ Strasbourg, Batiment CRBS Fac Med, Biopathol Myeline Neuroprotect & Strategies Therap, INSERM U1119,Federat Med Translationnelle Strasbou, 1 Rue Eugene Boeckel, F-67000 Strasbourg, France
关键词
Neurosteroidogenesis; Spinal cord; Pain; Neurosteroid; Neuroprotection; Peripheral nerve; CHAIN CLEAVAGE ENZYME; RAT SENSORY NEURONS; NEUROPATHIC PAIN; ANTINOCICEPTIVE PROPERTIES; BIOLOGICAL-ACTIVITY; CALCIUM-CHANNELS; 3-ALPHA-HYDROXYSTEROID OXIDOREDUCTASE; 3-BETA-HYDROXYSTEROID DEHYDROGENASE; NEUROACTIVE STEROIDS; GENE-EXPRESSION;
D O I
10.1016/j.yfrne.2023.101116
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The brain and spinal cord (SC) are both targeted by various hormones, including steroid hormones. However, investigations of the modulatory role of hormones on neurobiological functions usually focus only on the brain. The SC received little attention although this structure pivotally controls motor and sensory functions. Here, we critically reviewed key data showing that the process of neurosteroid biosynthesis or neurosteroidogenesis occurring in the SC plays a pivotal role in the modulation of peripheral nerve injury-induced chronic pain (PNICP) or neuropathic pain. Indeed, several active steroidogenic enzymes expressed in the SC produce endogenous neurosteroids that interact with receptors of neurotransmitters controlling pain. The spinal neurosteroidogenesis is differentially regulated during PNICP condition and its blockade modifies painful sensations. The paper suggests that future investigations aiming to develop effective strategies against PNICP or neuropathic pain must integrate in a gender or sex dependent manner the regulatory effects exerted by spinal neurosteroidogenesis.
引用
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页数:10
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