Department of Pharmacology and Pharmacodynamics, Medical University, Chodzki 4a, 20-093 Lublin, Poland.
Department of Drug Addiction Pharmacology, Maj Institute of Pharmacology, Polish Academy of Sciences, Smetna 12, 31-343 Kraków, Poland.
Int J Mol Sci. 2022 Feb 14;23(4):2122. doi: 10.3390/ijms23042122.
Mephedrone, a synthetic cathinone, is widely abused by adolescents and young adults. The aim of this study was to determine: (i) whether prior mephedrone exposure would alter ethanol reward and (ii) whether age and matrix metalloproteinase-9 (MMP-9) are important in this regard. In our research, male Wistar rats at postnatal day 30 (PND30) received mephedrone at the dose of 10 mg/kg, i.p., 3 times a day for 7 days. To clarify the role of MMP-9 in the mephedrone effects, one mephedrone-treated group received minocycline, as an MMP-9 antagonist. Animals were then assigned to conditioned place preference (CPP) procedure at PND38 (adolescent) or at PND69 (adult). After the CPP test (PND48/79), expression of dopamine D1 receptors (D1R), Cav1.2 (a subtype of L-type calcium channels), and MMP-9 was quantified in the rat ventral striatum (vSTR). The influence of mephedrone administration on the N-methyl-D-aspartate glutamate receptors (NMDAR) subunits (GluN1, GluN2A, and GluN2B) was then assessed in the vSTR of adult rats (only). These results indicate that, in contrast with adolescent rats, adult rats with prior mephedrone administration appear to be more sensitive to the ethanol effect in the CPP test under the drug-free state. The mephedrone effect in adult rats was associated with upregulation of D1R, NMDAR/GluN2B, MMP-9, and Cav1.2 signaling. MMP-9 appears to contribute to these changes in proteins expression because minocycline pretreatment blocked mephedrone-evoked sensitivity to ethanol reward. Thus, our results suggest that prior mephedrone exposure differentially alters ethanol reward in adolescent and adult rats.
麦角酸二乙酰胺,一种合成的卡西酮,被青少年和年轻人广泛滥用。本研究的目的是确定:(i)麦角酸二乙酰胺暴露是否会改变乙醇奖赏,以及(ii)年龄和基质金属蛋白酶-9(MMP-9)是否对此很重要。在我们的研究中,雄性 Wistar 大鼠在出生后第 30 天(PND30)时接受麦角酸二乙酰胺,剂量为 10mg/kg,腹腔内注射,每天 3 次,共 7 天。为了阐明 MMP-9 在麦角酸二乙酰胺作用中的作用,一组麦角酸二乙酰胺处理的大鼠接受米诺环素,作为 MMP-9 拮抗剂。然后,动物在 PND38(青少年)或 PND69(成年)时被分配到条件性位置偏好(CPP)程序。CPP 测试(PND48/79)后,在大鼠腹侧纹状体(vSTR)中定量测定多巴胺 D1 受体(D1R)、Cav1.2(L 型钙通道的一种亚型)和 MMP-9 的表达。然后在成年大鼠的 vSTR 中评估麦角酸二乙酰胺给药对 N-甲基-D-天冬氨酸谷氨酸受体(NMDAR)亚基(GluN1、GluN2A 和 GluN2B)的影响(仅)。这些结果表明,与青少年大鼠相比,先前给予麦角酸二乙酰胺的成年大鼠在无药物状态下的 CPP 测试中对乙醇的作用似乎更为敏感。成年大鼠的麦角酸二乙酰胺作用与 D1R、NMDAR/GluN2B、MMP-9 和 Cav1.2 信号的上调有关。MMP-9 似乎有助于这些蛋白表达的变化,因为米诺环素预处理阻断了麦角酸二乙酰胺引起的对乙醇奖赏的敏感性。因此,我们的结果表明,先前的麦角酸二乙酰胺暴露在青少年和成年大鼠中对乙醇奖赏产生不同的影响。