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感觉神经在大鼠虹膜小动脉而非扩约肌的功能中起传出作用。

Sensory nerves play an efferent role in the function of the arterioles, but not the dilator muscle, of the rat iris.

作者信息

Hill C E, Gould D J, Strigas J, Burcher E, Vidovic M

机构信息

Division of Neuroscience, John Curtin School of Medical Research, Australian National University, Canberra, Australia.

出版信息

J Auton Nerv Syst. 1996 Apr 20;58(1-2):89-100. doi: 10.1016/0165-1838(95)00126-3.

Abstract

We have studied the expression, distribution and function of receptors for the sensory neurotransmitters, substance P (SP) and calcitonin gene-related peptide (CGRP) in the dilator muscle and arterioles of the rat iris. Immunohistochemical studies showed that the sensory fibres containing these peptides are distributed throughout the connective tissue stroma of the iris and in association with the larger arterioles, but do not come into close association with the dilator muscle cells. Using reverse-transcription polymerase chain reaction, we have shown that both NK1 and NK3 receptor message is expressed by iris tissue, comprising both dilator muscle and stromal tissue. Binding sites for the NK1 agonist, [Sar9, Met(O2)11]-substance P (SarSP), and for CGRP are confined to the stromal layer and to the larger arterioles within that layer and do not appear to be associated with the dilator muscle itself. Application of either SarSP or CGRP produced both a vasodilatation and an inhibition of sympathetic nerve-induced vasoconstriction of the larger arterioles. Neither SarSP nor CGRP altered the resting tone of the dilator nor were they capable of modulating the contractions due to sympathetic nervous activity. These results suggest that the sensory fibres perform an efferent role in the larger irideal arterioles while their presence in the irideal stroma appears not to modulate the activity of the dilator muscle.

摘要

我们研究了感觉神经递质P物质(SP)和降钙素基因相关肽(CGRP)的受体在大鼠虹膜开大肌和小动脉中的表达、分布及功能。免疫组织化学研究表明,含有这些肽的感觉纤维分布于虹膜的整个结缔组织基质中,并与较大的小动脉相关,但不与开大肌细胞紧密相连。利用逆转录聚合酶链反应,我们发现虹膜组织(包括开大肌和基质组织)均表达NK1和NK3受体信息。NK1激动剂[Sar9,Met(O2)11]-P物质(SarSP)和CGRP的结合位点局限于基质层及其内较大的小动脉,似乎与开大肌本身无关。应用SarSP或CGRP均可使较大小动脉血管舒张,并抑制交感神经诱导的血管收缩。SarSP和CGRP均未改变开大肌的静息张力,也无法调节交感神经活动引起的收缩。这些结果表明,感觉纤维在较大的虹膜小动脉中发挥传出作用,而它们在虹膜基质中的存在似乎并未调节开大肌的活动。

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