Hypolipemic effects of histamine is due to inhibition of VLDL secretion from the liver: involvement of both H1 and H2-receptors.
Cholesterol
VLDL
histamine
lipid
liver
rat
Journal
Archives of physiology and biochemistry
ISSN: 1744-4160
Titre abrégé: Arch Physiol Biochem
Pays: England
ID NLM: 9510153
Informations de publication
Date de publication:
Dec 2022
Dec 2022
Historique:
pubmed:
25
6
2020
medline:
25
10
2022
entrez:
25
6
2020
Statut:
ppublish
Résumé
The research was performed to study the mechanism whereby histamine affects the profile of plasma lipids. Six groups of ten male rats were received two injections with histamine or its H1- and H2-agonists and antagonists. Histamine caused a significant decrease in the concentrations of triglyceride, total cholesterol, and LDLc, while HDLc had no significant change. The rate of VLDL secretion was 263.6 ± 25.8 mg/h dL in control rats and was inhibited by about 68% in histamine injected rats. These changes have been mimicked by either histamine H1- or H2-agonists. The effects of H1- and H2-agonists were abolished in the presence of cetirizine and famotidine respectively. Histamine causes a significant decrease in serum triglyceride, total, and LDL-cholesterol by both H1 and H2-receptors. The decrease in serum lipids is due to the inhibitory effect of histamine or its agonists on VLDL secretion from the liver.
Identifiants
pubmed: 32579487
doi: 10.1080/13813455.2020.1782436
doi:
Substances chimiques
Receptors, Histamine H2
0
Histamine
820484N8I3
Famotidine
5QZO15J2Z8
Receptors, Histamine H1
0
Cetirizine
YO7261ME24
Histamine Agonists
0
Triglycerides
0
Cholesterol
97C5T2UQ7J
Lipids
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM