Vascular dysfunction in ocular blood flow regulation impact of reactive oxygen species in an experimental setup

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Vascular dysfunction in ocular blood flow regulation impact of reactive oxygen species in an experimental setup. / Wagenfeld, Lars; Weiss, Sonja; Klemm, Maren; Richard, Gisbert; Zeitz, Oliver.

in: INVEST OPHTH VIS SCI, Jahrgang 55, Nr. 9, 2014, S. 5531-6.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{0c8c5daf1bd341f8adae0b5a018d2e8d,
title = "Vascular dysfunction in ocular blood flow regulation impact of reactive oxygen species in an experimental setup",
abstract = "PURPOSE: Glaucoma is associated with an altered blood flow and increased levels of reactive oxygen species (ROS). Reactive oxygen species can have opposing influences on the tone of a vessel; depending on the condition and type of the vessel, ROS can induce vasodilation or vasoconstriction. In the present study, we investigated the impact of ROS on the tone of rat ophthalmic arteries under various conditions and present data on the underlying mechanisms.METHODS: Freshly dissected rat ophthalmic arteries were pressurized in a perfusion setup to 80 mm Hg, at which a stable myogenic tone was observed. After various pretreatments (e.g., removal of endothelium, partial depolarization to -41 mV, blocking of the Na(+)/Ca(2+)-exchanger (NCX) in reverse mode by KB-R7943, or blocking of the Na(+)/K(+)-ATPase by ouabain), the vessels were exposed to ROS. Vessel diameter was continuously recorded and values before and after treatment compared.RESULTS: Stable myogenic tone of vessels with and without endothelium was established at a pressure of 80 mm Hg. At the physiological resting membrane potential, ROS exposure led to a significant vasodilatation, which was significantly reduced by pretreatment with ouabain. After depolarization to -41 mV, ROS exposure led to vasoconstriction. Blocking the NCX in reverse mode using KB-R7943 completely abolished this ROS-induced vasoconstriction.CONCLUSIONS: At resting potential, ROS provoke dilation; however, in precontracted vessels they act synergistically and induce further vasoconstriction. In diseases involving altered blood flow through altered vascular tone (e.g., vasospasms), ROS may influence blood flow and may thereby contribute indirectly to further disease progression.",
keywords = "Animals, Blood Pressure, Dilatation, Pathologic, Disease Models, Animal, Endothelium, Vascular, Muscle, Smooth, Vascular, Ophthalmic Artery, Rats, Rats, Wistar, Reactive Oxygen Species, Regional Blood Flow",
author = "Lars Wagenfeld and Sonja Weiss and Maren Klemm and Gisbert Richard and Oliver Zeitz",
note = "Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.",
year = "2014",
doi = "10.1167/iovs.14-14032",
language = "English",
volume = "55",
pages = "5531--6",
journal = "INVEST OPHTH VIS SCI",
issn = "0146-0404",
publisher = "Association for Research in Vision and Ophthalmology Inc.",
number = "9",

}

RIS

TY - JOUR

T1 - Vascular dysfunction in ocular blood flow regulation impact of reactive oxygen species in an experimental setup

AU - Wagenfeld, Lars

AU - Weiss, Sonja

AU - Klemm, Maren

AU - Richard, Gisbert

AU - Zeitz, Oliver

N1 - Copyright 2014 The Association for Research in Vision and Ophthalmology, Inc.

PY - 2014

Y1 - 2014

N2 - PURPOSE: Glaucoma is associated with an altered blood flow and increased levels of reactive oxygen species (ROS). Reactive oxygen species can have opposing influences on the tone of a vessel; depending on the condition and type of the vessel, ROS can induce vasodilation or vasoconstriction. In the present study, we investigated the impact of ROS on the tone of rat ophthalmic arteries under various conditions and present data on the underlying mechanisms.METHODS: Freshly dissected rat ophthalmic arteries were pressurized in a perfusion setup to 80 mm Hg, at which a stable myogenic tone was observed. After various pretreatments (e.g., removal of endothelium, partial depolarization to -41 mV, blocking of the Na(+)/Ca(2+)-exchanger (NCX) in reverse mode by KB-R7943, or blocking of the Na(+)/K(+)-ATPase by ouabain), the vessels were exposed to ROS. Vessel diameter was continuously recorded and values before and after treatment compared.RESULTS: Stable myogenic tone of vessels with and without endothelium was established at a pressure of 80 mm Hg. At the physiological resting membrane potential, ROS exposure led to a significant vasodilatation, which was significantly reduced by pretreatment with ouabain. After depolarization to -41 mV, ROS exposure led to vasoconstriction. Blocking the NCX in reverse mode using KB-R7943 completely abolished this ROS-induced vasoconstriction.CONCLUSIONS: At resting potential, ROS provoke dilation; however, in precontracted vessels they act synergistically and induce further vasoconstriction. In diseases involving altered blood flow through altered vascular tone (e.g., vasospasms), ROS may influence blood flow and may thereby contribute indirectly to further disease progression.

AB - PURPOSE: Glaucoma is associated with an altered blood flow and increased levels of reactive oxygen species (ROS). Reactive oxygen species can have opposing influences on the tone of a vessel; depending on the condition and type of the vessel, ROS can induce vasodilation or vasoconstriction. In the present study, we investigated the impact of ROS on the tone of rat ophthalmic arteries under various conditions and present data on the underlying mechanisms.METHODS: Freshly dissected rat ophthalmic arteries were pressurized in a perfusion setup to 80 mm Hg, at which a stable myogenic tone was observed. After various pretreatments (e.g., removal of endothelium, partial depolarization to -41 mV, blocking of the Na(+)/Ca(2+)-exchanger (NCX) in reverse mode by KB-R7943, or blocking of the Na(+)/K(+)-ATPase by ouabain), the vessels were exposed to ROS. Vessel diameter was continuously recorded and values before and after treatment compared.RESULTS: Stable myogenic tone of vessels with and without endothelium was established at a pressure of 80 mm Hg. At the physiological resting membrane potential, ROS exposure led to a significant vasodilatation, which was significantly reduced by pretreatment with ouabain. After depolarization to -41 mV, ROS exposure led to vasoconstriction. Blocking the NCX in reverse mode using KB-R7943 completely abolished this ROS-induced vasoconstriction.CONCLUSIONS: At resting potential, ROS provoke dilation; however, in precontracted vessels they act synergistically and induce further vasoconstriction. In diseases involving altered blood flow through altered vascular tone (e.g., vasospasms), ROS may influence blood flow and may thereby contribute indirectly to further disease progression.

KW - Animals

KW - Blood Pressure

KW - Dilatation, Pathologic

KW - Disease Models, Animal

KW - Endothelium, Vascular

KW - Muscle, Smooth, Vascular

KW - Ophthalmic Artery

KW - Rats

KW - Rats, Wistar

KW - Reactive Oxygen Species

KW - Regional Blood Flow

U2 - 10.1167/iovs.14-14032

DO - 10.1167/iovs.14-14032

M3 - SCORING: Journal article

C2 - 25034604

VL - 55

SP - 5531

EP - 5536

JO - INVEST OPHTH VIS SCI

JF - INVEST OPHTH VIS SCI

SN - 0146-0404

IS - 9

ER -