Ramshini Effat, Alaei Hojjatallah, Reisi Parham, Naghdi Naser, Afrozi Hossein, Alaei Samaneh, Alehashem Maryam, Eftekharvaghefi Shahrzad
Department of Physiology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran.
Department of Physiology, Pasteur Institute of Iran, Tehran, Iran.
Iran J Basic Med Sci. 2019 Mar;22(3):246-250. doi: 10.22038/ijbms.2019.28478.6925.
Many studies have focused on ventral tegmental area than of other mesocorticolimbic areas, and implicated a key role for the medial prefrontal cortex (mPFC) in the development of addictive behaviors. So far, the role of gamma-aminobutyric acid (GABA) receptors in the discriminative properties of morphine has received little attention and few studies evaluated the role of these receptors in drug dependence. Hence, we investigated the role of this receptor on morphine- induced GABA/ glutamate (GLU) changes in the mPFC following morphine administration using microdialysis.
In this study, 60 rats weighing 270-300 g were divided into six groups. First, microdialysis probe was inserted into the mPFC and was perfused with artificial cerebrospinal fluid and collected the baseline samples in all groups. In saline and morphine groups, the saline, in phaclophen and (phaclofen+morphine) groups, phaclofen (100 nmol), and in bicuculline and (bicuculline+morphine) groups, bicuculline (20 nmol) was injected intracerebroventricular. In saline, phaclofen and bicuculline groups 20 min later, animals received saline (0.2 ml, IP) and others groups received morphine (20 mg/kg, IP).
Our results showed that morphine increased the average concentration of GABA and decreased the concentration of GLU within mPFC. Pretreatment with phaclofen and bicuculline 20 min before morphine administration had no effect on GABA and GLU release for 100 min.
The present study indicated that morphine influence the GABA and GLU transmission in mPFC. Therefore evaluation of neurochemistry changes of this neural circuitry may provide further insight into the mechanisms underlying drug dependence.
许多研究聚焦于腹侧被盖区而非其他中脑皮质边缘区域,并认为内侧前额叶皮质(mPFC)在成瘾行为的发展中起关键作用。到目前为止,γ-氨基丁酸(GABA)受体在吗啡辨别特性中的作用很少受到关注,且很少有研究评估这些受体在药物依赖中的作用。因此,我们使用微透析技术研究了该受体在吗啡给药后对mPFC中吗啡诱导的GABA/谷氨酸(GLU)变化的作用。
在本研究中,将60只体重270 - 300 g的大鼠分为六组。首先,将微透析探针插入mPFC,并用人工脑脊液灌注,收集所有组的基线样本。在生理盐水组和吗啡组中,注射生理盐水;在荷包牡丹碱组和(荷包牡丹碱 + 吗啡)组中,脑室内注射荷包牡丹碱(100 nmol);在荷包牡丹碱组和(荷包牡丹碱 + 吗啡)组中,脑室内注射荷包牡丹碱(20 nmol)。20分钟后,在生理盐水组、荷包牡丹碱组和荷包牡丹碱组中,动物腹腔注射生理盐水(0.2 ml),其他组腹腔注射吗啡(20 mg/kg)。
我们的结果表明,吗啡增加了mPFC内GABA的平均浓度并降低了GLU的浓度。在吗啡给药前20分钟用荷包牡丹碱和荷包牡丹碱预处理100分钟对GABA和GLU释放没有影响。
本研究表明,吗啡影响mPFC中的GABA和GLU传递。因此,评估该神经回路的神经化学变化可能有助于进一步深入了解药物依赖的潜在机制。