Taniguchi T, Kawase K, Gu Z B, Kimura M, Okano Y, Kawakami H, Tsuji A, Kitazawa Y
Department of Ophthalmology, Gifu University School of Medicine, Gifu, Japan.
Exp Eye Res. 1999 Nov;69(5):467-74. doi: 10.1006/exer.1999.0737.
The purpose of this study was to determine the expression and effects of adrenomedullin (AM), a novel vasodilator peptide, in the eye. Expression of AM mRNA was examined in the rat iris-ciliary body using reverse transcription-polymerase chain reaction (RT-PCR). In rabbits, intraocular pressure (IOP) was measured periodically after intravitreal injection (20 microl) of AM (10(-7)-10(-4)m) into one eye. In separate groups of rabbits, 30 min after intravitreal injection of either AM-(22-52) (10(-3)m), a specific AM receptor antagonist, or CGRP-(8-37) (10(-3)m), a CGRP1 receptor antagonist, into one eye, AM (10(-6)m) was injected into both eyes, and IOP was measured. Using different rabbits, aqueous protein and cAMP concentrations were determined 6 hr after injection of AM. Expression of AM mRNA was detected in the rat iris-ciliary body. In rabbits, intravitreally administered AM (10(-6)-10(-4)m) profoundly lowered IOP, and the maximum effect was observed at 4-8 h. The ocular hypotensive effect of AM was dose-dependent (10(-7)-10(-4)m). Pretreatment with CGRP-(8-37) did not significantly inhibit the ocular hypotensive effect of AM (10(-6)m), whereas pretreatment with AM-(22-52) completely abolished it. AM (10(-6)m) did not significantly affect aqueous protein concentration. The higher dose of AM (10(-5)m) induced a significant increase in aqueous protein, which was not associated with an increase in the aqueous cAMP content and was significantly inhibited by AM-(22-52) and CGRP-(8-37). These results demonstrate that AM is expressed in the iris-ciliary body and decreases IOP mainly via specific AM receptors, and suggest that AM may play a role in controlling IOP.
本研究的目的是确定一种新型血管舒张肽——肾上腺髓质素(AM)在眼中的表达及作用。采用逆转录-聚合酶链反应(RT-PCR)检测大鼠虹膜睫状体中AM mRNA的表达。在兔中,向一只眼玻璃体内注射(20微升)AM(10⁻⁷ - 10⁻⁴摩尔)后定期测量眼压。在兔的不同组中,向一只眼玻璃体内注射AM-(22 - 52)(10⁻³摩尔)(一种特异性AM受体拮抗剂)或CGRP-(8 - 37)(10⁻³摩尔)(一种CGRP1受体拮抗剂)30分钟后,向双眼注射AM(10⁻⁶摩尔),并测量眼压。使用不同的兔,注射AM 6小时后测定房水蛋白和cAMP浓度。在大鼠虹膜睫状体中检测到AM mRNA的表达。在兔中,玻璃体内注射AM(10⁻⁶ - 10⁻⁴摩尔)可显著降低眼压,最大效应在4 - 8小时观察到。AM的降眼压作用呈剂量依赖性(10⁻⁷ - 10⁻⁴摩尔)。用CGRP-(8 - 37)预处理并未显著抑制AM(10⁻⁶摩尔)的降眼压作用,而用AM-(22 - 52)预处理则完全消除了该作用。AM(10⁻⁶摩尔)对房水蛋白浓度无显著影响。较高剂量的AM(10⁻⁵摩尔)可导致房水蛋白显著增加,这与房水cAMP含量增加无关,且被AM-(22 - 52)和CGRP-(8 - 37)显著抑制。这些结果表明,AM在虹膜睫状体中表达,主要通过特异性AM受体降低眼压,并提示AM可能在控制眼压中发挥作用。