Department of Pharmacology, Medical University of Innsbruck, Innsbruck, Austria.
Laura Bassi Centre of Expertise-THERAPEP, Research Program for Receptor Biochemistry and Tumor Metabolism, Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria.
Epilepsia. 2018 Nov;59(11):e166-e171. doi: 10.1111/epi.14573. Epub 2018 Oct 8.
There exists solid evidence that endogenous galanin and galanin agonists exert anticonvulsive actions mediated both by galanin 1 receptor (GAL1-R) and galanin 2 receptor (GAL2-R). We have now investigated whether depletion of the recently identified third galanin receptor, GAL3-R, and that of GAL2-R, alters the threshold to the systemically applied γ-aminobutyric acid (GABA) antagonist pentylenetetrazole (PTZ) or to intrahippocampally administered kainic acid (KA). In neither model, GAL3-KO mice differed in their latency to the first seizure, mean seizure duration, total number of seizures, or time spent in seizures compared to wild-type controls. In addition, consistent with previous data, the response to PTZ was not altered in GAL2-KO mice. In contrast, intrahippocampal KA resulted in a significantly increased number of seizures and time spent in seizures in GAL2-KO mice, although the latency to the first seizure and the duration of individual seizures was not altered. These results are consistent with the previous data showing that GAL2-R knockdown does not affect the number of perforant path stimulations required for initiating status epilepticus but significantly increases the seizure severity during the ongoing status. In conclusion, our data support a specific role of GAL2-R but not of GAL3-R in mediating the anticonvulsive actions of endogenous galanin.
有确凿证据表明,内源性甘丙肽及其激动剂通过甘丙肽 1 型受体(GAL1-R)和甘丙肽 2 型受体(GAL2-R)发挥抗惊厥作用。我们现在研究了最近发现的第三种甘丙肽受体 GAL3-R 和 GAL2-R 的耗竭是否会改变系统应用 γ-氨基丁酸(GABA)拮抗剂戊四氮(PTZ)或海马内给予的红藻氨酸(KA)的阈值。在这两种模型中,GAL3-KO 小鼠与野生型对照相比,首次癫痫发作的潜伏期、平均癫痫持续时间、总发作次数或发作时间均无差异。此外,与先前的数据一致,GAL2-KO 小鼠对 PTZ 的反应没有改变。相比之下,海马内 KA 导致 GAL2-KO 小鼠的发作次数和发作时间明显增加,尽管首次发作的潜伏期和单个发作的持续时间没有改变。这些结果与先前的数据一致,表明 GAL2-R 敲低不会影响引发癫痫持续状态所需的穿通通路刺激次数,但会显著增加持续癫痫发作时的癫痫严重程度。总之,我们的数据支持 GAL2-R 而不是 GAL3-R 在介导内源性甘丙肽的抗惊厥作用中的特定作用。