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缓激肽、血管活性肠肽、降钙素基因相关肽和神经肽 Y 的血管活性作用取决于体外猪视网膜小动脉的血管周围组织。

The vasoactive effects of bradykinin, vasoactive intestinal peptide, calcitonin gene-related peptide and neuropeptide Y depend on the perivascular tissue in porcine retinal arterioles in vitro.

机构信息

Department of Ophthalmology, Aarhus University Hospital, Aarhus N, Denmark.

出版信息

Acta Ophthalmol. 2024 May;102(3):349-356. doi: 10.1111/aos.15742. Epub 2023 Aug 11.

DOI:10.1111/aos.15742
PMID:37565361
Abstract

PURPOSE

The retina contains a number of vasoactive neuropeptides and corresponding receptors, but the role of these neuropeptides for tone regulation of retinal arterioles has not been studied in detail.

METHODS

Porcine arterioles with preserved perivascular retinal tissue were mounted in a wire myograph, and the tone was measured after the addition of increasing concentrations of bradykinin, vasoactive intestinal peptide (VIP), neuropeptide Y (NPY), substance P (SP), calcitonin gene-related peptide (CGRP) and brain natriuretic peptide (BNP). The experiments were performed during inhibition of the synthesis of nitric oxide (NO), prostaglandins and dopamine and were repeated after removal of the perivascular retinal tissue.

RESULTS

Bradykinin, VIP and CGRP induced significant concentration-dependent dilatation and NPY significant concentration-dependent contraction of the arterioles in the presence of perivascular retinal tissue (p < 0.03 for all comparisons) but not on isolated arterioles. BNP and SP had no effect on vascular tone. The NOS inhibitor L-NAME reduced bradykinin- and VIP-induced relaxation (p < 0.001 for both comparisons), whereas none of the other inhibitors influenced the vasoactive effects of the studied neuropeptides.

CONCLUSION

The effects of neuropeptides on the tone of retinal arterioles depend on the perivascular retinal tissue and may involve effects other than those mediated by nitric oxide, prostaglandins and adrenergic compounds. Investigation of the mechanisms underlying the vasoactive effect of neuropeptides may be important for understanding and treating retinal diseases where disturbances in retinal flow regulation are involved in the disease pathogenesis.

摘要

目的

视网膜含有多种血管活性神经肽及其相应的受体,但这些神经肽在调节视网膜小动脉张力方面的作用尚未得到详细研究。

方法

将保留血管周围视网膜组织的猪小动脉置于金属丝肌动描记器中,在加入逐渐增加浓度的缓激肽、血管活性肠肽(VIP)、神经肽 Y(NPY)、P 物质(SP)、降钙素基因相关肽(CGRP)和脑钠肽(BNP)后测量其张力。实验在抑制一氧化氮(NO)、前列腺素和多巴胺合成的情况下进行,并在去除血管周围视网膜组织后重复进行。

结果

在存在血管周围视网膜组织的情况下,缓激肽、VIP 和 CGRP 诱导小动脉产生显著的浓度依赖性舒张,而 NPY 则诱导小动脉产生显著的浓度依赖性收缩(所有比较均 p<0.03),但在分离的小动脉中则无此作用。BNP 和 SP 对血管张力没有影响。一氧化氮合酶抑制剂 L-NAME 减少了缓激肽和 VIP 诱导的舒张(两种比较均 p<0.001),而其他抑制剂均未影响研究中神经肽的血管活性作用。

结论

神经肽对视网膜小动脉张力的影响取决于血管周围的视网膜组织,可能涉及到除一氧化氮、前列腺素和肾上腺素能化合物以外的作用机制。研究神经肽的血管活性作用的机制对于理解和治疗涉及视网膜血流调节紊乱的视网膜疾病可能非常重要。

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