Suárez-Pereira Irene, López-Martín Carolina, Camarena-Delgado Carmen, Llorca-Torralba Meritxell, González-Saiz Francisco, Ruiz Rocío, Santiago Martiniano, Berrocoso Esther
Biomedical Research Networking Center for Mental Health (CIBERSAM), Institute of Health Carlos III (ISCIII), Madrid, Spain; Neuropsychopharmacology and Psychobiology Research Group, Department of Neuroscience, Faculty of Medicine, University of Cádiz, Cádiz, Spain; Biomedical Research and Innovation Institute of Cádiz (INIBICA), Puerta del Mar University Hospital, Cádiz, Spain.
Biomedical Research and Innovation Institute of Cádiz (INIBICA), Puerta del Mar University Hospital, Cádiz, Spain; IRCCS Humanitas Research Hospital, Milan, Italy; Institute of Neuroscience (IN-CNR), National Research Council of Italy, Milan, Italy.
Anesthesiology. 2024 Jul 1;141(1):131-150. doi: 10.1097/ALN.0000000000005006.
Dynamic changes in neuronal activity and in noradrenergic locus coeruleus (LC) projections have been proposed during the transition from acute to chronic pain. Thus, the authors explored the cellular cFos activity of the LC and its projections in conjunction with spontaneous pain-like behavior in neuropathic rats.
Tyrosine hydroxylase:Cre and wild-type Long-Evans rats, males and females, were subjected to chronic constriction injury (CCI) for 2 (short-term, CCI-ST) or 30 days (long-term, CCI-LT), evaluating cFos and Fluoro-Gold expression in the LC, and its projections to the spinal cord (SC) and rostral anterior cingulate cortex (rACC). These tests were carried out under basal conditions (unstimulated) and after noxious mechanical stimulation. LC activity was evaluated through chemogenetic and pharmacologic approaches, as were its projections, in association with spontaneous pain-like behaviors.
CCI-ST enhanced basal cFos expression in the LC and in its projection to the SC, which increased further after noxious stimulation. Similar basal activation was found in the neurons projecting to the rACC, although this was not modified by stimulation. Strong basal cFos expression was found in CCI-LT, specifically in the projection to the rACC, which was again not modified by stimulation. No cFos expression was found in the CCI-LT LCipsilateral (ipsi)/contralateral (contra)→SC. Chemogenetics showed that CCI-ST is associated with greater spontaneous pain-like behavior when the LCipsi is blocked, or by selectively blocking the LCipsi→SC projection. Activation of the LCipsi or LCipsi/contra→SC dampened pain-like behavior. Moreover, Designer Receptor Exclusively Activated by Designer Drugs (DREADDs)-mediated inactivation of the CCI-ST LCipsi→rACC or CCI-LT LCipsi/contra→rACC pathway, or intra-rACC antagonism of α-adrenoreceptors, also dampens pain-like behavior.
In the short term, activation of the LC after CCI attenuates spontaneous pain-like behaviors via projections to the SC while increasing nociception via projections to the rACC. In the long term, only the projections from the LC to the rACC contribute to modulate pain-like behaviors in this model.
在从急性疼痛向慢性疼痛转变的过程中,神经元活动以及去甲肾上腺素能蓝斑(LC)投射存在动态变化。因此,作者探讨了LC及其投射的细胞cFos活性,并结合神经病理性大鼠的自发性疼痛样行为进行研究。
对雄性和雌性酪氨酸羟化酶:Cre和野生型Long-Evans大鼠进行慢性缩窄性损伤(CCI),持续2天(短期,CCI-ST)或30天(长期,CCI-LT),评估LC及其向脊髓(SC)和喙前扣带回皮质(rACC)投射中的cFos和氟金表达。这些测试在基础条件下(未刺激)和有害机械刺激后进行。通过化学遗传学和药理学方法评估LC活性及其投射,并将其与自发性疼痛样行为相关联。
CCI-ST增强了LC及其向SC投射中的基础cFos表达,有害刺激后进一步增加。在投射到rACC的神经元中发现了类似的基础激活,尽管这种激活未被刺激所改变。在CCI-LT中发现了强烈的基础cFos表达,特别是在向rACC的投射中,同样未被刺激所改变。在CCI-LT的LC同侧(ipsi)/对侧(contra)→SC中未发现cFos表达。化学遗传学表明,当阻断LCipsi或选择性阻断LCipsi→SC投射时,CCI-ST与更严重的自发性疼痛样行为相关。激活LCipsi或LCipsi/contra→SC可减轻疼痛样行为。此外,设计药物特异性激活的设计受体(DREADDs)介导的CCI-ST LCipsi→rACC或CCI-LT LCipsi/contra→rACC通路失活,或rACC内α-肾上腺素能受体拮抗,也可减轻疼痛样行为。
短期内,CCI后LC的激活通过向SC的投射减轻自发性疼痛样行为,同时通过向rACC的投射增加伤害感受。长期来看,在该模型中,只有从LC到rACC的投射有助于调节疼痛样行为。