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[哌仑西平对形觉剥夺性近视豚鼠眼组织中M型乙酰胆碱受体表达的影响]

[Effect on of pirenzepine on expression of mAChRs in the ocular tissues of guinea pig with form-deprived myopia].

作者信息

Liu Qiong, Yu Jian, Zeng Jun-wen

机构信息

Department of Ophthalmology, Nanfang Hospital, Nanfang University, Guangzhou 510515, China.

出版信息

Zhonghua Yan Ke Za Zhi. 2010 Mar;46(3):221-6.

Abstract

OBJECTIVE

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.

METHODS

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.

RESULT

  1. After 21 days' treatment, FDM group produced relative myopia of -4.92 D and an axial length of 0.29 mm with significance (P < 0.001), compared with N group. Compared with group S, the relative refractive error in group P was +0.88 D, and axial length decreased 0.30 mm with respectively significance (P < 0.001). Differences in refractive error between group S and group FDM were not significant, but in axial length were significant (0.08 mm vs. 0.29 mm) (P < 0.05). 2. Semi-quantitative RT-PCR: M(1) and M(4) mRNA expression showed no significant differences in the retina, choroid and iris-ciliary body of group P compared with group S (P > 0.05). Of interest, in the posterior sclera, mRNA expression of group P was significantly greater than that of group S for the M(1) (P < 0.05) and M(4) subtypes (P < 0.05). The M(1) and M(4) subtype in group P was increased by +19.16% and +64.29% respectively.

CONCLUSION

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.

摘要

目的

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。

方法

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。

结果

  1. 治疗21天后,与N组相比,FDM组产生了-4.92 D的相对近视,眼轴长度增加0.29 mm,差异有统计学意义(P < 0.001)。与S组相比,P组的相对屈光不正为+0.88 D,眼轴长度减少0.30 mm,差异均有统计学意义(P < 0.001)。S组与FDM组之间的屈光不正差异无统计学意义,但眼轴长度差异有统计学意义(0.08 mm对0.29 mm)(P < 0.05)。2. 半定量RT-PCR:与S组相比,P组视网膜、脉络膜及虹膜睫状体中M(1)和M(4) mRNA表达差异无统计学意义(P > 0.05)。有趣的是,在后部巩膜中,P组M(1)(P < 0.05)和M(4)亚型(P < 0.05)的mRNA表达明显高于S组。P组M(1)和M(4)亚型分别增加了+19.16%和+64.29%。

结论

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。

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