Kumar Ashok, Foster Thomas C
Department of Neuroscience, McKnight Brain Institute, University of Florida, Gainesville, Florida.
Hippocampus. 2014 Apr;24(4):466-75. doi: 10.1002/hipo.22240. Epub 2014 Jan 14.
The susceptibility, but not the magnitude, of long-term depression (LTD) induced by hippocampal CA3-CA1 synaptic activity (synaptic-LTD) increases with advanced age. In contrast, the magnitude of LTD induced by pharmacological activation of CA3-CA1 group I metabotropic glutamate receptors (mGluRs) increases during aging. This study examined the signaling pathways involved in induction of LTD and the interaction between paired-pulse low frequency stimulation-induced synaptic-LTD and group I mGluR selective agonist, (RS)-3,5-dihydroxyphenylglycine (DHPG, 100 µM)-induced DHPG-LTD in hippocampal slices obtained from aged (22-24 months) male Fischer 344 rats. Prior induction of synaptic-LTD did not affect induction of DHPG-LTD; however, prior induction of the DHPG-LTD occluded synaptic-LTD suggesting that expression of DHPG-LTD may incorporate synaptic-LTD mechanisms. Application of individual antagonist for the group I mGluR (AIDA), the N-methyl-d-aspartate receptor (NMDAR) (AP-5), or L-type voltage-dependent Ca(2+) channel (VDCC) (nifedipine) failed to block synaptic-LTD and any two antagonists severely impaired synaptic-LTD induction, indicating that activation of any two mechanisms is sufficient to induce synaptic-LTD in aged animals. For DHPG-LTD, AIDA blocked DHPG-LTD and individually applied NMDAR or VDCC attenuated but did not block DHPG-LTD, indicating that the magnitude of DHPG-LTD depends on all three mechanisms.
海马CA3-CA1突触活动诱导的长时程抑制(LTD,即突触性LTD)的易感性会随年龄增长而增加,但幅度不变。相比之下,由CA3-CA1 I组代谢型谷氨酸受体(mGluRs)的药理学激活所诱导的LTD幅度在衰老过程中会增加。本研究检测了衰老(22 - 24个月)雄性Fischer 344大鼠海马切片中,LTD诱导所涉及的信号通路,以及配对脉冲低频刺激诱导的突触性LTD与I组mGluR选择性激动剂(RS)-3,5-二羟基苯甘氨酸(DHPG,100 μM)诱导的DHPG-LTD之间的相互作用。突触性LTD的预先诱导并不影响DHPG-LTD的诱导;然而,DHPG-LTD的预先诱导会阻断突触性LTD,这表明DHPG-LTD的表达可能纳入了突触性LTD机制。单独应用I组mGluR拮抗剂(艾达)、N-甲基-D-天冬氨酸受体(NMDAR)拮抗剂(AP-5)或L型电压依赖性钙通道(VDCC)拮抗剂(硝苯地平)均未能阻断突触性LTD,而任意两种拮抗剂联合应用则会严重损害突触性LTD的诱导,这表明激活任意两种机制就足以在衰老动物中诱导突触性LTD。对于DHPG-LTD,艾达可阻断DHPG-LTD,单独应用NMDAR或VDCC拮抗剂可减弱但不能阻断DHPG-LTD,这表明DHPG-LTD的幅度取决于所有这三种机制。