Diabetes Mellitus, Inflammation, Obesity: Proposed Treatment Pathways for Current and Future Therapies

被引:20
作者
Sonnett, Travis E. [1 ]
Levien, Terri L. [2 ]
Gates, Brian J. [2 ]
Robinson, Jennifer D. [1 ]
Campbell, R. Keith [1 ]
机构
[1] Washington State Univ, Dept Pharmacotherapy, Coll Pharm, Pullman, WA 99164 USA
[2] Washington State Univ, Dept Pharmacotherapy, Coll Pharm, Spokane, WA USA
关键词
adiponectin; diabetes mellitus; ghrelin; leptin; resveratrol; PLASMA ADIPONECTIN LEVELS; GHRELIN RECEPTOR AGONIST; INSULIN-RESISTANCE; METABOLIC SYNDROME; PPAR-GAMMA; GASTROINTESTINAL MOTILITY; PROTEIN ADIPONECTIN; GLUCOSE-HOMEOSTASIS; OXIDATIVE STRESS; SIRT1; ACTIVATION;
D O I
10.1345/aph.1M640
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
OBJECTIVE: To review the pathophysiology, pharmacology, and current or future therapies under study for use in treating diabetes mellitus, inflammation associated with diabetes mellitus, and/or obesity related to diabetes mellitus, through 1 of 4 investigational pathways: adiponectin, ghrelin, resveratrol, or leptin. DATA SOURCES: A literature search using MEDLINE (1966 December 12, 2009), Pub Med (1950 December 12, 2009), Science Direct (1994 December 12, 2009), and International Pharmaceutical Abstracts (1970 December 12, 2009) was performed using the terms adiponectin, ghrelin, resveratrol, leptin, inflammation, obesity, and diabetes mellitus. English-language, original research, and review articles were examined, and citations from these articles were assessed as well. STUDY SELECTION AND DATA EXTRACTION: Clinical studies and in vitro studies were included in addition to any Phase 1, 2, or 3 clinical trials. DATA SYNTHESIS: Mechanistic pathways regarding adiponectin, ghrelin, resveratrol, and leptin are of interest as future treatment options for diabetes mellitus. Each of these pathways has produced significant in vitro and in vivo clinical data warranting further research as a possible treatment pathway for diabetes-related inflammation and/or obesity reduction. While research is still underway to determine the exact effects these pathways have on metabolic function, current data suggest that each of these compounds may be of interest for future therapies. CONCLUSIONS: While several pathways under investigation may offer additional benefits in the treatment of diabetes mellitus and associated impairments, further investigation is necessary for both investigational and approved therapies to ensure that the impact in new pathways does not increase risks to patient safety and outcomes.
引用
收藏
页码:701 / 711
页数:11
相关论文
共 125 条
[1]
Role of leptin in the neuroendocrine response to fasting [J].
Ahima, RS ;
Prabakaran, D ;
Mantzoros, C ;
Qu, DQ ;
Lowell, B ;
MaratosFlier, E ;
Flier, JS .
NATURE, 1996, 382 (6588) :250-252
[2]
Advanced glycation endproducts - role in pathology of diabetic complications [J].
Ahmed, N .
DIABETES RESEARCH AND CLINICAL PRACTICE, 2005, 67 (01) :3-21
[3]
Sirt1 regulates aging and resistance to oxidative stress in the heart [J].
Alcendor, Ralph R. ;
Gao, Shumin ;
Zhai, Peiyong ;
Zablocki, Daniela ;
Holle, Eric ;
Yu, Xianzhong ;
Tian, Bin ;
Wagner, Thomas ;
Vatner, Stephen F. ;
Sadoshima, Junichi .
CIRCULATION RESEARCH, 2007, 100 (10) :1512-1521
[4]
Ameri M, 2007, IRAN J SCI TECHNOL B, V31, P1
[5]
[Anonymous], DIAB WHAT IS DIAB
[6]
Glimepiride increases high-density lipoprotein cholesterol via increasing adiponectin levels in type 2 diabetes mellitus [J].
Araki, Takahiro ;
Emoto, Masanori ;
Konishi, Toshiaki ;
Ikuno, Yoshiko ;
Lee, Eiko ;
Teramura, Megumi ;
Motoyama, Koka ;
Yokoyama, Hisayo ;
Mori, Katsuhito ;
Koyama, Hidenori ;
Shoji, Tetsuo ;
Nishizawa, Yoshiki .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2009, 58 (02) :143-148
[7]
Adipocyte-derived plasma protein adiponectin acts as a platelet-derived growth factor-BB-binding protein and regulates growth factor-induced common postreceptor signal in vascular smooth muscle cell [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Maeda, K ;
Kuriyama, H ;
Okamoto, Y ;
Kumada, M ;
Hotta, K ;
Nishida, M ;
Takahashi, M ;
Nakamura, T ;
Shimomura, I ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
CIRCULATION, 2002, 105 (24) :2893-2898
[8]
The stomach is a source of leptin [J].
Bado, A ;
Levasseur, S ;
Attoub, S ;
Kermorgant, S ;
Laigneau, JP ;
Bortoluzzi, MN ;
Moizo, L ;
Lehy, T ;
Guerre-Millo, M ;
Le Marchand-Brustel, Y ;
Lewin, MJM .
NATURE, 1998, 394 (6695) :790-793
[9]
Beltowski Jerzy, 2008, Cardiovascular & Hematological Disorders - Drug Targets, V8, P7, DOI 10.2174/187152908783884920
[10]
ACRP30/adiponectin: an adipokine regulating glucose and lipid metabolism [J].
Berg, AH ;
Combs, TP ;
Scherer, PE .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2002, 13 (02) :84-89