1993
DOI: 10.1007/bf00229785
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Component-specific effects of physostigmine on the cat visual evoked potential

Abstract: Pattern visual evoked potentials (VEPs) were recorded from the pial surface of the cat primary visual cortex prior to and following the intravenous administration of physostigmine, an agent which blocks the enzyme responsible for the breakdown of synaptically released acetylcholine. The control VEP was composed of a small initial positive deflection (P1), a subsequent large negative wave (N1) and a second large positive wave (P2). Following physostigmine, the amplitude of P1-N1 was diminished whereas that of N… Show more

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Cited by 26 publications
(14 citation statements)
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“…In the superior colliculus of rats treated with 0.4 mg/kg of PHY, Hetzler and Melk [51] confirmed that the amplitudes of P1 and P3 components were depressed and the P4 component was enhanced. These results support the hypothesis that each VEP component may be modulated in its own way, depending on the drug, the dose, the animal model and the recording techniques [50].…”
Section: Discussionsupporting
confidence: 78%
See 1 more Smart Citation
“…In the superior colliculus of rats treated with 0.4 mg/kg of PHY, Hetzler and Melk [51] confirmed that the amplitudes of P1 and P3 components were depressed and the P4 component was enhanced. These results support the hypothesis that each VEP component may be modulated in its own way, depending on the drug, the dose, the animal model and the recording techniques [50].…”
Section: Discussionsupporting
confidence: 78%
“…After 1 mg/kg of PHY in rats, an amplitude reduction in the middle component and an increase in the first component was shown [46]. 0.4 mg/kg of PHY in the rat at f-VEP [47,48] and 0.8 mg/kg in the cat at pattern reversal VEPs [49] suppressed all amplitude component; on the other hand, after 1 mg/kg Arakawa et al [50] showed only a reduction in the P1N1 component. In the superior colliculus of rats treated with 0.4 mg/kg of PHY, Hetzler and Melk [51] confirmed that the amplitudes of P1 and P3 components were depressed and the P4 component was enhanced.…”
Section: Discussionmentioning
confidence: 99%
“…The VEP latency, however, was modulated in an opposite way. Our results support the assumption that each VEP component may be modulated in its own way [17], The contradictory EEG and VEP changes after drug applica tion may be explained by different direct or indirect drug effects on the hippocampus (EEG) and on the occipital neocortex (VEP). However, further experiments with si multaneous EEG records within the dorsal hippocampus and the occipital neocortex are necessary to separate the participation of both regions in the generation of the oc cipital electrocorticogram.…”
Section: Discussionsupporting
confidence: 76%
“…Such response characteristics respectively follow the known contrast response functions of the parvocellular and magnocellular pathways to sinusoidal luminance gratings (Benardete et al 1992;Benardete and Kaplan 1997a,b;Derrington and Lennie 1984;Merigan and Eskin 1986;Merigan and Maunsell 1993;Tootell et al 1988). Additionally, both C1 and P1 components have been shown to be pharmacologically separable in the cat visual cortex (e.g., Arakawa et al 1993;Zemon et al 1980) and are differentially modulated by cathodal or anodal stimulation in transcranial direct current stimulation (tDCS) paradigms with human participants (Accornero et al 2007;Antal et al 2004). The pharmacological separability of the C1 and P1 VEP components in cats and differential modulation of the same components in humans using tDCS would both be expected if each component were generated by different neural populations.…”
mentioning
confidence: 56%