Department of Anatomy and Neurobiology, School of Medicine, UPR-MSC, PO Box 365067, San Juan, PR 00936-5067, USA.
Pharmacol Biochem Behav. 2012 May;101(3):369-78. doi: 10.1016/j.pbb.2012.01.016. Epub 2012 Jan 24.
Anxiety disorders are more prevalent in females than males. The underlying reasons for this gender difference are unknown. Metabotropic glutamate receptors (mGluRs) have been linked to anxiety and it has been shown that interaction between estrogen receptors and mGluRs modulate sexual receptivity in rats. We investigated the role of mGluRs in anxiety-related behaviors in ovariectomized female rats with (OVX+EB) or without (OVX) estradiol implants. We centrally infused (s)-3,5-dihydroxyphenylglycine (DHPG), a group I mGluR agonist, into the basolateral amygdala (BLA) of OVX+EB and OVX rats at 0.1 and 1.0 μM. Male rats that normally have low estradiol levels were used to compare with OVX rats. Generalized anxiety, explorative activity and detection and analysis of threat were analyzed in the elevated plus maze (EPM) and risk assessment behaviors (RABs). DHPG (1.0 μM) increased the percentage of time spent in- and entries into- the open arms in OVX+EB, but not in OVX or male rats. Flat-back approaches and stretch-attend postures, two RABs, were significantly reduced by DHPG (0.1 and 1.0 μM) in OVX+EB rats only. DHPG did not modulate rearing and freezing, behaviors related to exploration and fear-like behavior, respectively. However, DHPG (1.0 μM) increased head dipping and decreased grooming behaviors in OVX rats, suggesting a weak explorative modulation. The effects of DHPG observed in OVX+EB, were blocked by 50 μM of (RS)-1-aminoindan-1,5-dicarboxylic acid (AIDA), a mGluR1 antagonist. AIDA and/or estradiol did not modulate anxiety and or RABs. Our results show that intra-BLA infusion of DHPG exerts an anxiolytic-like effect in OVX+EB, but not in OVX or male rats. This effect seems to depend upon mGluR1 subtype activation. Our findings led us to suggest that the effects observed in OVX+EB rats might be due to an interaction at the membrane level of estrogen receptors with mGlu1 within the BLA.
焦虑症在女性中比男性更为普遍。这种性别差异的根本原因尚不清楚。代谢型谷氨酸受体(mGluRs)与焦虑有关,并且已经表明雌激素受体与 mGluRs 的相互作用调节大鼠的性接受性。我们研究了在有(OVX+EB)或没有(OVX)雌激素植入物的去卵巢雌性大鼠中,mGluRs 在焦虑相关行为中的作用。我们将(S)-3,5-二羟苯甘氨酸(DHPG),一种 I 组 mGluR 激动剂,以 0.1 和 1.0 μM 的浓度经中央输注到外侧杏仁核(BLA)中OVX+EB 和 OVX 大鼠。通常具有低雌激素水平的雄性大鼠用于与 OVX 大鼠进行比较。在高架十字迷宫(EPM)中分析了一般焦虑,探索性活动以及威胁的检测和分析,以及风险评估行为(RABs)。DHPG(1.0 μM)增加了 OVX+EB 大鼠进入和进入开放臂的时间百分比,但OVX 或雄性大鼠则没有。只有在 OVX+EB 大鼠中,DHPG(0.1 和 1.0 μM)才显著减少了平背方法和伸展注意姿势,这两种 RAB。DHPG 没有调节分别与探索和恐惧样行为有关的后肢抬高和冻结行为。然而,DHPG(1.0 μM)增加了 OVX 大鼠的头浸行为,并减少了梳理行为,表明探索性调节作用较弱。在 OVX+EB 中观察到的 DHPG 作用被 50 μM(RS)-1-氨基茚烷-1,5-二羧酸(AIDA)阻断,AIDA 是 mGluR1 拮抗剂。AIDA 和/或雌激素对焦虑或 RABs 没有调节作用。我们的研究结果表明,BLA 内 DHPG 的输注在 OVX+EB 中产生了类似抗焦虑的作用,但在 OVX 或雄性大鼠中则没有。这种作用似乎取决于 mGluR1 亚型的激活。我们的发现使我们认为,在 OVX+EB 大鼠中观察到的作用可能是由于雌激素受体与 BLA 内的 mGlu1 在膜水平上的相互作用所致。