Ault B, Nadler J V
Br J Pharmacol. 1983 Apr;78(4):701-8. doi: 10.1111/j.1476-5381.1983.tb09423.x.
1 The effects of baclofen were tested on epileptiform discharge in the rat hippocampal slice. Slices were superfused with bicuculline methiodide (100 microM) and maximal periods of afterdischarge were evoked by stimulating the Schaffer collateral-commissural pathway in area CA1, mossy fibres in area CA3 or perforant path fibres in the fascia dentata or by antidromic stimulation of CA1 pyramidal cells. 2 (-)-Baclofen attenuated the afterdischarge evoked by stimulating all three sets of fibres in areas CA1 and CA3. In each case, a threshold effect was observed at a concentration of 0.25 or 0.5 microM, and complete suppression was usually attained with a concentration of 5 microM. EC50 values ranged between 1 and 2 microM. (-)-Baclofen attenuated hippocampal afterdischarge with 120 times the potency of (+)-baclofen. It did not, however, affect the repetitive firing of dentate granule cells in response to stimulation of perforant path fibres. 3 (-)-Baclofen also reduced the amplitude of the initial population spike evoked by stimulation of Schaffer collateral-commissural fibres, but did not affect the antidromic population spike nor the initial population spike evoked by stimulation of the mossy fibres. 4 Recurrent inhibition in area CA1 was abolished by 1 microM (-)-baclofen. Thus baclofen, unlike many anticonvulsants, does not suppress afterdischarge by potentiating GABAergic inhibition. 5 These results suggest that baclofen attenuates hippocampal afterdischarge by a combination of pre- and postsynaptic mechanisms.
测试了巴氯芬对大鼠海马切片癫痫样放电的影响。将切片用甲磺酸荷包牡丹碱(100微摩尔)进行灌流,并通过刺激CA1区的Schaffer侧支-连合通路、CA3区的苔藓纤维、齿状回的穿通通路纤维或对CA1锥体细胞进行逆向刺激来诱发最大后放电期。
(-)-巴氯芬减弱了刺激CA1区和CA3区所有三组纤维所诱发的后放电。在每种情况下,在浓度为0.25或0.5微摩尔时观察到阈值效应,通常在浓度为5微摩尔时可实现完全抑制。半数有效浓度(EC50)值在1至2微摩尔之间。(-)-巴氯芬减弱海马后放电的效力是(+)-巴氯芬的120倍。然而,它并不影响齿状颗粒细胞对穿通通路纤维刺激的重复放电。
(-)-巴氯芬还降低了刺激Schaffer侧支-连合纤维所诱发的初始群体峰电位的幅度,但不影响逆向群体峰电位或刺激苔藓纤维所诱发的初始群体峰电位。
1微摩尔(-)-巴氯芬消除了CA1区的回返性抑制。因此,与许多抗惊厥药不同,巴氯芬不是通过增强GABA能抑制来抑制后放电。
这些结果表明,巴氯芬通过突触前和突触后机制的组合来减弱海马后放电。