PMID- 37604668 OWN - NLM STAT- MEDLINE DCOM- 20230823 LR - 20240417 IS - 2051-817X (Electronic) IS - 2051-817X (Linking) VI - 11 IP - 16 DP - 2023 Aug TI - Differential effect of gold nanoparticles on cerebrovascular function and biomechanical properties. PG - e15789 LID - 10.14814/phy2.15789 [doi] LID - e15789 AB - Human stroke serum (HSS) has been shown to impair cerebrovascular function, likely by factors released into the circulation after ischemia. 20 nm gold nanoparticles (GNPs) have demonstrated anti-inflammatory properties, with evidence that they decrease pathologic markers of ischemic severity. Whether GNPs affect cerebrovascular function, and potentially protect against the damaging effects of HSS on the cerebral circulation remains unclear. HSS obtained 24 h poststroke was perfused through the lumen of isolated and pressurized third-order posterior cerebral arteries (PCAs) from male Wistar rats with and without GNPs (~2 x 10(9) GNP/ml), or GNPs in vehicle, in an arteriograph chamber (n = 8/group). All vessels were myogenically reactive >/=60 mmHg intravascular pressure; however, vessels containing GNPs had significantly less myogenic tone. GNPs increased vasoreactivity to small and intermediate conductance calcium activated potassium channel activation via NS309; however, reduced vasoconstriction to nitric oxide synthase inhibition. Hydraulic conductivity and transvascular filtration, were decreased by GNPs, suggesting a protective effect on the blood-brain barrier. The stress-strain curves of PCAs exposed to GNPs were shifted leftward, indicating increased vessel stiffness. This study provides the first evidence that GNPs affect the structure and function of the cerebrovasculature, which may be important for their development and use in biomedical applications. CI - (c) 2023 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. FAU - Hunt, Ryan D AU - Hunt RD AUID- ORCID: 0009-0009-7899-5152 AD - Department of Neurological Sciences, University of Vermont Larner College of Medicine, Burlington, Vermont, USA. FAU - Sedighi, Omid AU - Sedighi O AUID- ORCID: 0000-0002-4766-7983 AD - Department of Electrical and Biomedical Engineering, University of Vermont College of Engineering and Mathematical Sciences, Burlington, Vermont, USA. FAU - Clark, Wayne M AU - Clark WM AD - Oregon Stroke Center, Department of Neurology, Oregon Health, and Science University, Portland, USA. FAU - Doiron, Amber L AU - Doiron AL AUID- ORCID: 0000-0002-6963-0989 AD - Department of Electrical and Biomedical Engineering, University of Vermont College of Engineering and Mathematical Sciences, Burlington, Vermont, USA. FAU - Cipolla, Marilyn J AU - Cipolla MJ AUID- ORCID: 0000-0002-9172-5941 AD - Department of Neurological Sciences, University of Vermont Larner College of Medicine, Burlington, Vermont, USA. AD - Department of Electrical and Biomedical Engineering, University of Vermont College of Engineering and Mathematical Sciences, Burlington, Vermont, USA. AD - Department of Obstetrics, Gynecology and Reproductive Sciences, University of Vermont Larner College of Medicine, Burlington, Vermont, USA. AD - Department of Pharmacology, University of Vermont Larner College of Medicine, Burlington, Vermont, USA. LA - eng GR - R01 NS093289/NS/NINDS NIH HHS/United States GR - U54 GM115516/GM/NIGMS NIH HHS/United States GR - S10 OD025030/OD/NIH HHS/United States GR - S10 RR019246/RR/NCRR NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PL - United States TA - Physiol Rep JT - Physiological reports JID - 101607800 RN - 7440-57-5 (Gold) SB - IM MH - Rats MH - Humans MH - Animals MH - Male MH - Rats, Wistar MH - *Gold/pharmacology MH - *Metal Nanoparticles MH - Angiography MH - Blood-Brain Barrier PMC - PMC10442527 OTO - NOTNLM OT - blood-brain barrier OT - cerebrovasculature OT - gold nanoparticles OT - ischemia OT - stroke COIS- The authors declare no competing interests. EDAT- 2023/08/22 00:41 MHDA- 2023/08/23 06:42 PMCR- 2023/08/21 CRDT- 2023/08/21 21:13 PHST- 2023/07/24 00:00 [revised] PHST- 2023/03/29 00:00 [received] PHST- 2023/07/24 00:00 [accepted] PHST- 2023/08/23 06:42 [medline] PHST- 2023/08/22 00:41 [pubmed] PHST- 2023/08/21 21:13 [entrez] PHST- 2023/08/21 00:00 [pmc-release] AID - PHY215789 [pii] AID - 10.14814/phy2.15789 [doi] PST - ppublish SO - Physiol Rep. 2023 Aug;11(16):e15789. doi: 10.14814/phy2.15789.