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Neuropeptide Y treatment induces retinal vasoconstriction and causes functional and histological retinal damage in a porcine ischaemia model

Christiansen, Anders T. (author)
Copenhagen University Hospital,University of Copenhagen
Sørensen, Nina B. (author)
Copenhagen University Hospital
Haanes, Kristian A. (author)
Copenhagen University Hospital
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Blixt, Frank W. (author)
Lund University,Lunds universitet,Experimentell kärlforskning,Forskargrupper vid Lunds universitet,Experimental Vascular Research,Lund University Research Groups
la Cour, Morten (author)
Copenhagen University Hospital
Warfvinge, Karin (author)
Copenhagen University Hospital
Klemp, Kristian (author)
Copenhagen University Hospital
Woldbye, David P.D. (author)
University of Copenhagen
Kiilgaard, Jens F. (author)
Copenhagen University Hospital
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 (creator_code:org_t)
2018-09-14
2018
English.
In: Acta Ophthalmologica. - : Wiley. - 1755-375X. ; 96:8, s. 812-820
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Purpose: To investigate the effects of intravitreal neuropeptide Y (NPY) treatment following acute retinal ischaemia in an in vivo porcine model. In addition, we evaluated the vasoconstrictive potential of NPY on porcine retinal arteries ex vivo. Methods: Twelve pigs underwent induced retinal ischaemia by elevated intraocular pressure clamping the ocular perfusion pressure at 5 mmHg for 2 hr followed by intravitreal injection of NPY or vehicle. After 4 weeks, retinas were evaluated functionally by standard and global-flash multifocal electroretinogram (mfERG) and histologically by thickness of retinal layers and number of ganglion cells. Additionally, the vasoconstrictive effects of NPY and its involved receptors were tested using wire myographs and NPY receptor antagonists on porcine retinal arteries. Results: Intravitreal injection of NPY after induced ischaemia caused a significant reduction in the mean induced component (IC) amplitude ratio (treated/normal eye) compared to vehicle-treated eyes. This reduction was accompanied by histological damage, where NPY treatment reduced the mean thickness of inner retinal layers and number of ganglion cells. In retinal arteries, NPY-induced vasoconstriction to a plateau of approximately 65% of potassium-induced constriction. This effect appeared to be mediated via Y1 and Y2, but not Y5. Conclusion: In seeming contrast to previous in vitro studies, intravitreal NPY treatment caused functional and histological damage compared to vehicle after a retinal ischaemic insult. Furthermore, we showed for the first time that NPY induces Y1- and Y2- but not Y5-mediated vasoconstriction in retinal arteries. This constriction could explain the worsening in vivo effect induced by NPY treatment following an ischaemic insult and suggests that future studies on exploring the neuroprotective effects of NPY might focus on other receptors than Y1 and Y2.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Oftalmologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Ophthalmology (hsv//eng)

Keyword

multifocal electroretinogram
neuropeptide Y
neuropeptide Y receptors
neuroprotection
retina
swine
vasoconstriction

Publication and Content Type

art (subject category)
ref (subject category)

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