Hypolipidemic effect of brown seaweed (Sargassum crassifolium) extract in vivo (Study of histopathology, mRNA expression, and immunohistochemistry (IHC) with VCAM-1, ICAM-1, and MCP-1 parameters)
The purpose of this study was to obtain natural drugs from brown seaweed (Sargassum crassifolium) as antiatherosclerosis candidates through the study of hypolipidemic mechanisms of action. Modeling of dyslipidemia rats was carried out by feeding high-fat (HFF) and doses of crude fucoidan 100. 200. 4...
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Zusammenfassung: | The purpose of this study was to obtain natural drugs from brown seaweed
(Sargassum crassifolium) as antiatherosclerosis candidates through the study of
hypolipidemic mechanisms of action. Modeling of dyslipidemia rats was carried
out by feeding high-fat (HFF) and doses of crude fucoidan 100. 200. 400mg /
KgBB. in both treatments measured blood lipid profile levels taken from the
orbital sinuses. HE's histopathology. mRNA expression. immunohistochemistry
(IHC) with parameters VCAM-1. ICAM-1. and MCP-1 were performed on adipose
tissue. as well as liver. Total cholesterol values 51.07-225.2. triglycerides
30.43-115.73. HDL 13.1-24.86 mg/dl and LDL 20.22-189.68 mg/dl. In the treatment
of crude fucoidan obtained the result of p value < {\alpha} (0.05.
Histopathological features of adipose tissue after administration of HFF for 60
days resulted in an increase in adipose cell size. and the liver experienced
structural damage and inflammation. but after 21 days of treatment the
morphological picture of adipose tissue was similar to normal morphology and
the liver also decreased in severity and inflammation. The results of
histochemical staining after treatment showed a positive staining part on
MCP-1. The result of p value < {\alpha} (0.05) of mRNA expression for
administration of 3 treatment doses. A dyslipidemic mouse model with HFF
administration for 60 days succeeded in becoming a dyslipidemic rat. and crude
fucoidan had hypolipidemic activity. Doses of 100. 200. and 400 mg/KgBB crude
fucoidan showed improvement in adipose and liver morphological features of
severity and inflammation of dyslipidemic rats and decreased mRNA expression. |
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DOI: | 10.48550/arxiv.2402.07497 |