Homocysteine and Asymmetrical Dimethylarginine in Diabetic Rats Treated with Docosahexaenoic Acid-Loaded Zinc Oxide Nanoparticles.


Journal

Applied biochemistry and biotechnology
ISSN: 1559-0291
Titre abrégé: Appl Biochem Biotechnol
Pays: United States
ID NLM: 8208561

Informations de publication

Date de publication:
Jul 2020
Historique:
received: 03 11 2019
accepted: 08 01 2020
pubmed: 22 1 2020
medline: 30 1 2021
entrez: 22 1 2020
Statut: ppublish

Résumé

Hyperglycemia, the hallmark of diabetes mellitus, is considered one of the endothelial dysfunction risk factors, the main reason of vascular complication. In this study, we aimed to evaluate homocysteine (Hcy) and asymmetrical dimethylarginine (ADMA) levels in diabetic rats and the possibility to attenuate the elevation of these two parameters by supplementation of docosahexaenoic acid (DHA) alone or loaded zinc oxide nanoparticles (ZnONPs) to improve endothelial dysfunction in streptozotocin (STZ)-induced diabetic rats. Forty male albino rats weighing 180-200 g were classified as control, diabetic, diabetic treated with DHA, and diabetic treated with DHA-loaded zinc oxide nanoparticles (DHA/ZnONPs) groups. Fasting blood glucose, insulin, ADMA, Hcy, and nitric oxide (NO) were estimated. Fatty acids (linoleic acid (LA), arachidonic acid (AA), DHA, α-linolenic acid (ALA), and oleic acid (OA)) were also evaluated by reversed phase HPLC using a UV detector. The results showed that fasting blood sugar, insulin resistance, LA, AA, OA, ADMA, and Hcy increased significantly in diabetic rats compared with control while fasting insulin, DHA, ALA, and NO decreased significantly in diabetic rats. In both treated groups, fasting blood sugar, insulin resistance, LA, AA, OA, ADMA, and Hcy significantly decreased as compared with the diabetic group while fasting insulin, DHA, ALA, and NO were significantly increased. In conclusion, DHA and DHA/ZnONP supplementation protect against diabetic complications and improve endothelial dysfunction as well as hyperhomocysteinemia in diabetes. DHA/ZnONP-treated group appeared more efficient than DHA alone.

Identifiants

pubmed: 31960366
doi: 10.1007/s12010-020-03230-z
pii: 10.1007/s12010-020-03230-z
doi:

Substances chimiques

Insulin 0
Homocysteine 0LVT1QZ0BA
Docosahexaenoic Acids 25167-62-8
Nitric Oxide 31C4KY9ESH
N,N-dimethylarginine 63CV1GEK3Y
Cellulose 9004-34-6
Arginine 94ZLA3W45F
Zinc Oxide SOI2LOH54Z

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1127-1139

Subventions

Organisme : National Research Centre
ID : (internal project no: 11010130).)

Auteurs

Jihan Hussein (J)

Medical Biochemistry Department, National Research Centre, Dokki, Giza, Egypt. jihan_husein@yahoo.com.

Mehrez El-Naggar (M)

Textile Research Division, National Research Centre, Dokki, Giza, Egypt.

Ehsan Badawy (E)

Medical Biochemistry Department, National Research Centre, Dokki, Giza, Egypt.

Nabila El-Laithy (N)

Medical Biochemistry Department, National Research Centre, Dokki, Giza, Egypt.

Maha El-Waseef (M)

Medical Biochemistry Department, National Research Centre, Dokki, Giza, Egypt.

Hanan Hassan (H)

Medical Biochemistry Department, National Research Centre, Dokki, Giza, Egypt.

Yasmin Abdel-Latif (Y)

Medical Biochemistry Department, National Research Centre, Dokki, Giza, Egypt.

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Classifications MeSH