The Natural-Mineral-Based Novel Nanomaterial IFMC Increases Intravascular Nitric Oxide without Its Intake: Implications for COVID-19 and beyond.

COVID-19 SARS-CoV-2 blood flow promotion haemoglobin natural-mineral-based nanomaterial nitric oxide

Journal

Nanomaterials (Basel, Switzerland)
ISSN: 2079-4991
Titre abrégé: Nanomaterials (Basel)
Pays: Switzerland
ID NLM: 101610216

Informations de publication

Date de publication:
29 Aug 2020
Historique:
received: 24 07 2020
revised: 16 08 2020
accepted: 27 08 2020
entrez: 3 9 2020
pubmed: 3 9 2020
medline: 3 9 2020
Statut: epublish

Résumé

There are currently no promising therapy strategies for either the treatment or prevention of novel coronavirus disease 2019 (COVID-19), despite the urgent need. In addition to respiratory diseases, vascular complications are rapidly emerging as a key threat of COVID-19. Existing nitric oxide (NO) therapies have been shown to improve the vascular system; however, they have different limitations in terms of safety, usability and availability. In light of this, we hypothesise that a natural-mineral-based novel nanomaterial, which was developed based on NO therapy, might be a viable strategy for the treatment and prevention of COVID-19. The present study examined if it could induce an increase of intravascular NO, vasodilation and the consequent increase of blood flow rate and temperature in a living body. The intravascular NO concentration in the hepatic portal of rats was increased by 0.17 nM over 35.2 s on average after its application. An ultrasonic Doppler flow meter showed significant increases in the blood flow rate and vessel diameter, but no difference in the blood flow velocity. These were corroborated by measurements of human hand surface temperature. To our knowledge, this result is the first evidence where an increase of intravascular NO and vasodilation were induced by bringing a natural-mineral-based nanomaterial into contact with or close to a living body. The precise mechanisms remain a matter for further investigation; however, we may assume that endothelial NO synthase, haemoglobin and endothelium-derived hyperpolarising factor are deeply involved in the increase of intravascular NO.

Identifiants

pubmed: 32872395
pii: nano10091699
doi: 10.3390/nano10091699
pmc: PMC7559745
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Tomohiro Akiyama (T)

Advanced Research Laboratories, Tokyo City University, Tokyo 158-8557, Japan.
Graduate School of Information Technology, Kobe Institute of Computing, Kobe 650-0001, Japan.
Graduate School of Education, Kyoto University, Kyoto 606-8501, Japan.
Graduate School of Global Environmental Studies, Sophia University, Tokyo 102-8554, Japan.

Takamichi Hirata (T)

Advanced Research Laboratories, Tokyo City University, Tokyo 158-8557, Japan.
Graduate School of Integrative Science and Engineering, Electrical Engineering and Chemistry, Tokyo City University, Tokyo 158-8557, Japan.

Takahiro Fujimoto (T)

Advanced Research Laboratories, Tokyo City University, Tokyo 158-8557, Japan.
Clinic F Laser Medicine & Surgery, Tokyo 102-0083, Japan.

Shinnosuke Hatakeyama (S)

Graduate School of Integrative Science and Engineering, Electrical Engineering and Chemistry, Tokyo City University, Tokyo 158-8557, Japan.

Ryuhei Yamazaki (R)

Graduate School of Integrative Science and Engineering, Electrical Engineering and Chemistry, Tokyo City University, Tokyo 158-8557, Japan.

Tomohiro Nomura (T)

Osaka City University, Osaka 558-8585, Japan.

Classifications MeSH