Verna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, Texas, USA.
Invest Ophthalmol Vis Sci. 2010 Jan;51(1):567-76. doi: 10.1167/iovs.09-4168. Epub 2009 Aug 6.
To characterize effects of the muscarinic antagonist atropine (A) and the alpha-adrenergic agonist, phenylephrine (P), on mydriasis and light-evoked signaling in mice anesthetized by ketamine and xylazine (K+X).
Pupillary areas of anesthetized C57BL/6 mice were measured, with or without topical application of A or A+P. Dark-adapted ERGs were recorded from 2- to 4-month-old C57BL/6 and 7.5-month-old albino hrhoG/hrhoG mice after application of A or P singly or in combination, before or after induction of K+X anesthesia. Effects of GABA were tested in the hrhoG/hrhoG mice.
K+X anesthesia resulted in maximum mydriasis that was not enhanced by A or A+P. Dark-adapted b-wave amplitudes (-1.3 log sc td s) after K+X anesthesia were similar with or without A or P. A+P in the presence of K+X produced a slow growth in b-wave amplitude, reaching a plateau of twofold enhancement in 1 hour. Recordings of responses to varying flash energies revealed that the effects of A+P were on the maximum amplitude of the a- and b-waves and not on their sensitivity. Scotopic threshold responses were augmented as well. In photoreceptor-degenerated mice (hrhoG/hrhoG), an electronegative ERG wave recorded with K+X+A, was converted to a gamma-aminobutyric acid (GABA)-sensitive response with two electropositive components with A+P after K+X.
Topical administration of A and P together, but not separately, in the presence of K+X, leads to a slow, dramatic enhancement of a- and b-waves by an unknown mechanism independent of pupil dilation.
研究毒蕈碱拮抗剂阿托品(A)和α-肾上腺素能激动剂苯肾上腺素(P)对氯胺酮和甲苯噻嗪(K+X)麻醉小鼠瞳孔散大和光诱发电信号的影响。
在麻醉的 C57BL/6 小鼠中测量瞳孔面积,同时或不使用 A 或 A+P 进行局部应用。在应用 A 或 P 单独或联合应用后,在 K+X 麻醉诱导之前或之后,从 2 至 4 个月大的 C57BL/6 和 7.5 个月大的白化 hrhoG/hrhoG 小鼠中记录暗适应 ERG。在 hrhoG/hrhoG 小鼠中测试 GABA 的作用。
K+X 麻醉导致最大瞳孔散大,A 或 A+P 不能增强。暗适应 b 波振幅(-1.3 log sc td s)在 K+X 麻醉后相似,有无 A 或 P。A+P 在 K+X 存在下产生 b 波振幅缓慢增长,在 1 小时内达到两倍增强的平台。对不同闪烁能量响应的记录表明,A+P 的作用是在 a-和 b-波的最大幅度上,而不是在其敏感性上。视锥细胞退化小鼠(hrhoG/hrhoG)中,K+X+A 记录的负电 ERG 波在 K+X 后用 A+P 转化为具有两个正电成分的 GABA 敏感反应。
在 K+X 存在下局部应用 A 和 P 一起,但不是单独应用,会导致 a-和 b-波的缓慢、显著增强,其机制未知,与瞳孔扩张无关。