Liu Qiong, Yu Jian, Zeng Jun-wen
Department of Ophthalmology, Nanfang Hospital, Nanfang University, Guangzhou 510515, China.
Zhonghua Yan Ke Za Zhi. 2010 Mar;46(3):221-6.
To study effects of vitreous injecting M(1)-selective muscarinic antagonist, pirenzepine, on expression of M(1) and M(4) receptor in retina, choroid, sclera and iris-ciliary body of guinea pig with form-deprived myopia.
Twenty-four 1 - 2 week-old pigmented guinea pigs were randomly divided into four groups. Group1: normal control (N) (n = 6); group 2: simple form-deprived myopia (FDM) (n = 6); group 3: drug control (S) (n = 6); group 4: pirenzepine (P) (n = 6). Expression changes of M(1) and M(4) muscarinic receptors at mRNA level were detected by semi-quantitative RT-PCR in retina, choroid, sclera and iris-ciliary body.
M(1)-selective muscarinic antagonist, pirenzepine, can effectively inhibit form-deprived myopia in guinea pig. M(1) and M(4) subtype in sclera and their cholinergic signaling may participate in muscarinic antagonist inhibition of myopic development.
研究玻璃体内注射M(1)选择性毒蕈碱拮抗剂哌仑西平对形觉剥夺性近视豚鼠视网膜、脉络膜、巩膜及虹膜睫状体中M(1)和M(4)受体表达的影响。
将24只1 - 2周龄的有色豚鼠随机分为四组。第1组:正常对照组(N)(n = 6);第2组:单纯形觉剥夺性近视组(FDM)(n = 6);第3组:药物对照组(S)(n = 6);第4组:哌仑西平组(P)(n = 6)。采用半定量逆转录聚合酶链反应(RT-PCR)检测视网膜、脉络膜、巩膜及虹膜睫状体中M(1)和M(4)毒蕈碱受体mRNA水平的表达变化。
M(1)选择性毒蕈碱拮抗剂哌仑西平可有效抑制豚鼠形觉剥夺性近视。巩膜中的M(1)和M(4)亚型及其胆碱能信号可能参与毒蕈碱拮抗剂对近视发展的抑制作用。