Kudo Y, Oka J I, Yamada K
Neurosci Lett. 1981 Aug 7;25(1):83-8. doi: 10.1016/0304-3940(81)90105-1.
The neuropharmacological properties of anisatin were tested on the frog spinal cord and the crude synaptic membrane from rat brain. Anisatin (10(-5) M) reduced the amplitude of dorsal root potentials induced by stimulation of the adjacent dorsal root and presynaptic inhibition of the ventral root reflex. Anisatin shifted the dose-response curve for GABA-induced depolarization in the primary afferent terminal to the right and also reduced the maximum response to GABA. [3H]Muscimol binding to the crude synaptic membrane was not inhibited by anisatin. These results indicate that anisatin is a picrotoxin-like, non-competitive GABA-antagonist.
在青蛙脊髓和大鼠脑粗制突触膜上测试了印防己毒素的神经药理学特性。印防己毒素(10^(-5) M)降低了刺激相邻背根所诱发的背根电位幅度以及腹根反射的突触前抑制。印防己毒素使初级传入终末中γ-氨基丁酸(GABA)诱导的去极化剂量-反应曲线右移,并且也降低了对GABA的最大反应。印防己毒素不抑制[3H]蝇蕈醇与粗制突触膜的结合。这些结果表明印防己毒素是一种类似印防己毒素的非竞争性GABA拮抗剂。