Muscle phenotype of AGAT- and GAMT-deficient mice after simvastatin exposure

Autor: Ricarda Grzybowski, Erik Hanff, Rainer H. Böger, D. Tsikas, Kathrin Cordts, Christian Gerloff, Axel Neu, Ali Sasani, Chi-Un Choe, Dirk Isbrandt, Sönke Hornig, Edzard Schwedhelm
Jazyk: angličtina
Rok vydání: 2020
Předmět:
0301 basic medicine
Simvastatin
metabolism [Muscle
Skeletal]

Clinical Biochemistry
drug effects [Gene Expression Regulation]
Biochemistry
metabolism [Homoarginine]
chemistry.chemical_compound
Mice
Myocyte
pharmacology [Simvastatin]
DNA Modification Methylases
antagonists & inhibitors [DNA Repair Enzymes]
genetics [DNA Repair Enzymes]
drug effects [Muscle
Skeletal]

Guanidinoacetate N-methyltransferase
Phenotype
ddc:540
genetics [Guanidinoacetate N-Methyltransferase]
Animal studies
antagonists & inhibitors [DNA Modification Methylases]
medicine.symptom
medicine.drug
Genetically modified mouse
medicine.medical_specialty
Statin
medicine.drug_class
metabolism [Arginine]
Arginine
Creatine
03 medical and health sciences
genetics [Tumor Suppressor Proteins]
Internal medicine
antagonists & inhibitors [Tumor Suppressor Proteins]
medicine
Animals
Humans
Muscle
Skeletal

Myopathy
metabolism [Creatine]
030102 biochemistry & molecular biology
business.industry
Tumor Suppressor Proteins
Organic Chemistry
genetics [DNA Modification Methylases]
nutritional and metabolic diseases
Homoarginine
DNA Repair Enzymes
030104 developmental biology
Endocrinology
Gene Expression Regulation
chemistry
deficiency [Guanidinoacetate N-Methyltransferase]
Guanidinoacetate N-Methyltransferase
business
Zdroj: Amino acids 52(1), 73-85 (2019). doi:10.1007/s00726-019-02812-4
DOI: 10.1007/s00726-019-02812-4
Popis: Statin-induced myopathy affects more than 10 million people worldwide. But discontinuation of statin treatment increases mortality and cardiovascular events. Recently, l-arginine:glycine amidinotransferase (AGAT) gene was associated with statin-induced myopathy in two populations, but the causal link is still unclear. AGAT is responsible for the synthesis of l-homoarginine (hArg) and guanidinoacetate (GAA). GAA is further methylated to creatine (Cr) by guanidinoacetate methyltransferase (GAMT). In cerebrovascular patients treated with statin, lower hArg and GAA plasma concentrations were found than in non-statin patients, indicating suppressed AGAT expression and/or activity (n = 272, P = 0.033 and P = 0.039, respectively). This observation suggests that statin-induced myopathy may be associated with AGAT expression and/or activity in muscle cells. To address this, we studied simvastatin-induced myopathy in AGAT- and GAMT-deficient mice. We found that simvastatin induced muscle damage and reduced AGAT expression in wildtype mice (myocyte diameter: 34.1 ± 1.3 µm vs 21.5 ± 1.3 µm, P = 0.026; AGAT expression: 1.0 ± 0.3 vs 0.48 ± 0.05, P = 0.017). Increasing AGAT expression levels of transgenic mouse models resulted in rising plasma levels of hArg and GAA (P
Databáze: OpenAIRE