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Effect of ketanserin tartrate on HMG CoA reductase and LDL receptor activity in cultured human skin fibroblasts
- Source :
- European Journal of Clinical Pharmacology. 39:217-220
- Publication Year :
- 1990
- Publisher :
- Springer Science and Business Media LLC, 1990.
-
Abstract
- In man ketanserin tartrate reduces plasma LDL cholesterol. To clarify the mechanism of this effect the effect of ketanserin on 3-hydroxy-3-methylglutaryl (HMG) CoA reductase and LDL receptor activity in cultured human skin fibroblasts has been examined. After incubation with ketanserin for 14 h HMG CoA reductase activity was decreased in a dose-dependent manner up to 300 ng/ml (550 nM) without changing the free cholesterol content in the cells. Ketanserin increased specific binding and specific internalization of 125I-LDL dose-dependently. There was a significant inverse relationship between the percentage changes in HMG CoA reductase and LDL receptor activity. It appears that ketanserin induces up-regulation of LDL receptor activity by direct suppression of HMG CoA reductase, and this may be one mechanism by which plasma LDL-cholesterol is reduced by ketanserin.
- Subjects :
- Adult
Male
medicine.medical_specialty
Ketanserin
media_common.quotation_subject
Reductase
chemistry.chemical_compound
Internal medicine
medicine
Humans
Pharmacology (medical)
Internalization
Cells, Cultured
Skin
media_common
Pharmacology
biology
Cholesterol
musculoskeletal, neural, and ocular physiology
General Medicine
Fibroblasts
musculoskeletal system
Hydroxymethylglutaryl-CoA reductase
Up-Regulation
Endocrinology
Receptors, LDL
Mechanism of action
chemistry
HMG-CoA reductase
LDL receptor
cardiovascular system
biology.protein
Hydroxymethylglutaryl CoA Reductases
lipids (amino acids, peptides, and proteins)
medicine.symptom
medicine.drug
Subjects
Details
- ISSN :
- 14321041 and 00316970
- Volume :
- 39
- Database :
- OpenAIRE
- Journal :
- European Journal of Clinical Pharmacology
- Accession number :
- edsair.doi.dedup.....6ab5b258c3312a2b64b9b226348d58c5
- Full Text :
- https://doi.org/10.1007/bf00315099