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Inhibition of key digestive enzymes related to hyperlipidemia and protection of liver-kidney functions by Cystoseira crinita sulphated polysaccharide in high-fat diet-fed rats
- Source :
- Biomedicinepharmacotherapy = Biomedecinepharmacotherapie. 85
- Publication Year :
- 2016
-
Abstract
- The objective of this current study was to investigate the possible hyperlipidemic and antioxidative effects of Cystoseira crinita sulfated polysaccharide (CCSP) in rats fed with a high-fat diet, exhibited an inhibitory activity on pancreatic lipase in vitro. In vivo administration of this extract to HFD-rats lowered body weight and potentially inhibited key enzymes of lipid metabolism and absorption as lipase activity in both plasma and small intestine, which led to a notable decrease of blood LDL- cholesterol (LDL-Ch) and triglycerides (TG) levels, and an increase in HDL-cholesterol (HDL-Ch) levels in HFD-rats. CCSP was also observed to protect the liver-kidney functions efficiently, by decreasing of aspartate transaminase (AST), alanine transaminase (ALT), lactate dehydrogenase (LDH) and Creatine phosphokinase (CPK) activities and creatinine, albumin, T-bilirubin, uric acid, and urea rates in plasma. The histological analysis of liver and kidney tissues further established the positive effect of CCSP.
- Subjects :
- 0301 basic medicine
Male
medicine.medical_specialty
Aspartate transaminase
Hyperlipidemias
Kidney
Phaeophyta
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Polysaccharides
Internal medicine
Lactate dehydrogenase
Hyperlipidemia
medicine
Animals
Rats, Wistar
Pharmacology
biology
Dose-Response Relationship, Drug
Cholesterol
Plant Extracts
Albumin
General Medicine
medicine.disease
Dietary Fats
Rats
030104 developmental biology
Endocrinology
chemistry
Alanine transaminase
Liver
030220 oncology & carcinogenesis
biology.protein
Uric acid
lipids (amino acids, peptides, and proteins)
Creatine kinase
Digestion
Subjects
Details
- ISSN :
- 19506007
- Volume :
- 85
- Database :
- OpenAIRE
- Journal :
- Biomedicinepharmacotherapy = Biomedecinepharmacotherapie
- Accession number :
- edsair.doi.dedup.....6b14bb0232f4130c8b02f7929bbbef21