[Effect on of pirenzepine on expression of mAChRs in the ocular tissues of guinea pig with form-deprived myopia].
Qiong Liu, Jian Yu, Junwen Zeng
Abstract
Qiong Liu, Jian Yu, Junwen Zeng
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.
OpenAlex reports 2 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
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.
Key concepts: Pirenzepine, Muscarinic acetylcholine receptor, Sclera, Muscarinic antagonist, Guinea pig, Choroid, Antagonist, Endocrinology