咪唑啉受体在调节房水动力学中的潜在作用。

W R Campbell, D E Potter
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引用次数: 12

摘要

1)将莫onidine (MOX)注射至NZW家兔前侧脑室,诱导双侧低血压(> 7.0 mmHg)持续2小时。2)将氧美唑啉(Oxymetazoline, OXY)注射到NZW兔的前侧脑室,诱导双侧低血压(> 7.0 mmHg),并在2 h达到峰值。3)单侧局部应用氧可诱导对侧和同侧眼在3小时内出现最大双侧低血压(> 12 mmHg),持续时间超过12小时。4)假定的咪唑啉(I1)拮抗剂依法罗森注射到前侧脑室,可显著抑制由icvt MOX、icvt OXY和单侧局部OXY引起的低血压。5)位于中枢神经系统的咪唑啉(I1)受体在MOX-和OXY诱导的低血压中发挥作用,推测的咪唑啉(I1)受体拮抗剂依法罗胺能够抑制MOX-、OXY-和局部OXY诱导的低血压。
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Potential role of imidazoline (I1) receptors in modulating aqueous humor dynamics.

1) Moxonidine (MOX), injected icvt into the anterior lateral ventricle of NZW rabbits, induced bilateral, ocular hypotension (> 7.0 mmHg) that persisted for two hrs. 2) Oxymetazoline (OXY), injected icvt into the anterior lateral ventricle of NZW rabbits, induced bilateral ocular hypotension (> 7.0 mmHg) that peaked at two hrs. 3) Unilateral topical application of OXY induced maximal, bilateral ocular hypotension (> 12 mmHg), at 3 hrs, in both the contralateral and ipsilateral eyes, that persisted more than 12 hrs. 4) The putative imidazoline (I1) antagonist, efaroxan, injected icvt into the anterior lateral ventricle, inhibited significantly the ocular hypotension produced by icvt MOX, icvt OXY, and unilateral topical OXY. 5) Imidazoline (I1) receptors, located in the CNS, play a role in MOX- and OXY-induced ocular hypotension, as suggested by the ability of the putative imidazoline (I1) receptor antagonist efaroxan, to inhibit icvt MOX-, icvt OXY- and topical OXY-induced ocular hypotension.

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