TY - JOUR
T1 - Approaches for the development of drugs for treatment of obesity and metabolic syndrome
AU - Maksimov, Maksim L.
AU - Svistunov, Andrey A.
AU - Tarasov, Vadim V.
AU - Chubarev, Vladimir N.
AU - Ávila-Rodriguez, Marco
AU - Barreto, George E.
AU - Dralova, Olga V.
AU - Aliev, Gjumrakch
N1 - Publisher Copyright:
© 2016 Bentham Science Publishers.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - Obesity and metabolic syndrome (MS) are risk factors for diabetes, cancer, some cardiovascular and musculoskeletal diseases. Pharmacotherapy should be used when the body mass index (BMI) exceeds 30 kg/m2 or 27 kg/m2 with comorbidity. Efficacy and safety of pharmacotherapy depend on the mechanism of action of drugs. In this context, drugs affecting the central and peripheral mediator systems such as cannabinoid receptor antagonists (Rimonabant), neuronal reuptake inhibitor of NE and 5-HT (Sibutramine), neuronal reuptake inhibitor of NE 5-HT DA (Tesofensine), agonist of 5-HT 2C receptors (Lorcaserin) have a high risk of side effects on the central nervous and cardiovascular systems when used for a long period. Apparently, the drugs design targeting obesity should screen safer drugs that affect fat absorption (Orlistat), activate energy metabolism (Adipokines), inhibit MetAP2 (Beloranib) and other peripheral metabolic processes. The use of synergies of anti-obesity drugs with different mechanisms of action is an effective approach for developing new combined pharmaceutical compositions (Contrave®, Empatic™, Qsymia et al.). The purpose of this article is to review the currently available anti-obesity drugs and some new promising trends in the development of anti-obesity therapy.
AB - Obesity and metabolic syndrome (MS) are risk factors for diabetes, cancer, some cardiovascular and musculoskeletal diseases. Pharmacotherapy should be used when the body mass index (BMI) exceeds 30 kg/m2 or 27 kg/m2 with comorbidity. Efficacy and safety of pharmacotherapy depend on the mechanism of action of drugs. In this context, drugs affecting the central and peripheral mediator systems such as cannabinoid receptor antagonists (Rimonabant), neuronal reuptake inhibitor of NE and 5-HT (Sibutramine), neuronal reuptake inhibitor of NE 5-HT DA (Tesofensine), agonist of 5-HT 2C receptors (Lorcaserin) have a high risk of side effects on the central nervous and cardiovascular systems when used for a long period. Apparently, the drugs design targeting obesity should screen safer drugs that affect fat absorption (Orlistat), activate energy metabolism (Adipokines), inhibit MetAP2 (Beloranib) and other peripheral metabolic processes. The use of synergies of anti-obesity drugs with different mechanisms of action is an effective approach for developing new combined pharmaceutical compositions (Contrave®, Empatic™, Qsymia et al.). The purpose of this article is to review the currently available anti-obesity drugs and some new promising trends in the development of anti-obesity therapy.
KW - Adipokines
KW - Beloranib
KW - Contrave®
KW - Empatic™
KW - Liraglutide
KW - Lorcaserin
KW - Orlistat
KW - Pharmacotherapy of obesity
KW - Qsymia
KW - Rimonabant
KW - Sibutramine
KW - Tesofensine
KW - Treatment of obesity and ms
UR - http://www.scopus.com/inward/record.url?scp=84958531487&partnerID=8YFLogxK
U2 - 10.2174/1381612822666151209153047
DO - 10.2174/1381612822666151209153047
M3 - Article
C2 - 26648466
AN - SCOPUS:84958531487
SN - 1381-6128
VL - 22
SP - 895
EP - 903
JO - Current Pharmaceutical Design
JF - Current Pharmaceutical Design
IS - 7
ER -