Neuroscience, Washington State University, Vancouver, Washington, USA.
R.S. Dow Neurobiology, Legacy Research Institute, Portland, Oregon, USA.
Addict Biol. 2023 Nov;28(11):e13334. doi: 10.1111/adb.13334.
The medial prefrontal cortex (mPFC) drives cocaine-seeking behaviour in rodent models of cocaine use disorder. Parvalbumin (PV)-containing GABAergic interneurons powerfully control the output of the mPFC, yet few studies have focused on how these neurons modulate cocaine-seeking behaviour. Most PV neurons are surrounded by perineuronal nets (PNNs), which regulate the firing of PV neurons. We examined staining intensity and number of PV and PNNs after long-access (6 h/day) cocaine self-administration in rats followed by either 8-10 days extinction ± cue-induced reinstatement or short-term (1-2 days) or long-term (30-31 days) abstinence ± cue-induced reinstatement. The intensity of PNNs was increased in the prelimbic and infralimbic PFC after long-term abstinence in the absence of cue reinstatement and after cue reinstatement following both daily extinction sessions and after a 30-day abstinence period. PV intensity was increased after 30 days of abstinence in the prelimbic but not infralimbic PFC. Enzymatic removal of PNNs with chondroitinase ABC (ABC) in the prelimbic PFC did not prevent incubation of cue-induced reinstatement but decreased cocaine-seeking behaviour at both 2 and 31 days of abstinence, and this decrease at 31 days was accompanied by reduced c-Fos levels in the prelimbic PFC. Increases in PNN intensity have generally been associated with the loss of plasticity, suggesting that the persistent and chronic nature of cocaine use disorder may in part be attributed to long-lasting increases in PNN intensity that reduce the ability of stimuli to alter synaptic input to underlying PV neurons.
内侧前额皮质(mPFC)驱动可卡因成瘾的啮齿动物模型中的可卡因觅药行为。含有 Parvalbumin(PV)的 GABA 能中间神经元有力地控制 mPFC 的输出,但很少有研究关注这些神经元如何调节可卡因觅药行为。大多数 PV 神经元都被围绕着 Perineuronal Nets(PNNs)包围,PNNs 调节 PV 神经元的放电。我们在大鼠进行长时程(每天 6 小时)可卡因自我给药后,观察了 8-10 天消退期±线索诱导复吸或短期(1-2 天)或长期(30-31 天)禁欲±线索诱导复吸后的 PV 和 PNN 染色强度和数量。在长期禁欲后(无线索复吸)以及在每日消退期后和 30 天禁欲期后进行线索复吸后,在额前皮质和下边缘皮质的 PNN 强度增加。在 30 天禁欲后,额前皮质中的 PV 强度增加,但下边缘皮质中没有增加。在额前皮质中用软骨素酶 ABC(ABC)去除 PNNs 并没有阻止线索诱导复吸的孵育,但减少了 2 天和 31 天禁欲期的可卡因觅药行为,并且在 31 天禁欲期,这种减少伴随着额前皮质中 c-Fos 水平的降低。PNN 强度的增加通常与可塑性的丧失有关,这表明可卡因成瘾的持续性和慢性特征可能部分归因于 PNN 强度的持久增加,从而降低了刺激改变潜在 PV 神经元突触输入的能力。