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Molecular and Cellular Mechanisms of Anti-Obesity Agents: An Integrative Review
Harmandeep Kaur1, Deepika Kaushik2, Prasad Rasane1
1Department of Food Technology and Nutrition, Lovely Professional University, Phagwara, Punjab, India.
Abstract:
Genes play a pivotal role in appetite regulation and energy homeostasis during a person's obesity. LEP (Leptin) and POMC (Proopiomelanocortin) are vital for appetite suppression and promoting satiety, while AgRP (Agouti-related peptide) and NPY (Neuropeptide Y) serve to stimulate appetite, creating a balanced interplay between hunger and satiety signals. GHRL (Ghrelin) further promotes hunger, emphasizing the complexity of these regulatory mechanisms. BDNF (Brain-derived neurotrophic factor) shows a dual role, impacting energy homeostasis not only in the brain but also in adipose tissue, thereby influencing lipid metabolism. PCSK1 (Proprotein Convertase Subtilisin/Kexin Type 1) is critical for the processing of neuropeptides that modulate energy balance. IGF2BP2 (Insulin-like Growth Factor 2 mRNA-Binding Protein 2) and MAP2K5 (Mitogen-Activated Protein Kinase 5) contribute to metabolic processes involved in fat accumulation and glucose regulation. Thus, emphasizing the significance of these mechanisms offers valuable insights that could lead to effective interventions for obesity prevention and management.
Insights
Genetic factors significantly influence appetite and energy balance in obesity. Key genes like Leptin (LEP) and Proopiomelanocortin (POMC) suppress appetite, while others stimulate it, highlighting complex regulatory pathways for obesity management.
Area of Science:
- Genetics and Molecular Biology
- Metabolic Regulation
- Neuroendocrinology
Background:
- Obesity is a complex metabolic disorder influenced by genetic factors affecting appetite and energy homeostasis.
- Several key genes and their protein products are known to regulate hunger and satiety signals within the body.
Purpose of the Study:
- To elucidate the pivotal roles of specific genes in appetite regulation and energy homeostasis.
- To highlight the significance of these genetic mechanisms for potential obesity interventions.
Main Methods:
- Review and synthesis of existing research on genes involved in appetite regulation.
- Analysis of the functions of specific genes including LEP, POMC, AgRP, NPY, GHRL, BDNF, PCSK1, IGF2BP2, and MAP2K5.
Main Results:
- Genes like Leptin (LEP) and Proopiomelanocortin (POMC) suppress appetite, while Agouti-related peptide (AgRP) and Neuropeptide Y (NPY) stimulate it.
- Ghrelin (GHRL) promotes hunger, and Brain-derived neurotrophic factor (BDNF) has a dual role in brain and adipose tissue.
- Proprotein Convertase Subtilisin/Kexin Type 1 (PCSK1), Insulin-like Growth Factor 2 mRNA-Binding Protein 2 (IGF2BP2), and Mitogen-Activated Protein Kinase 5 (MAP2K5) are critical for neuropeptide processing and metabolic regulation.
Conclusions:
- The intricate interplay of these genes is crucial for maintaining energy balance.
- Understanding these genetic mechanisms provides valuable insights for developing effective strategies for obesity prevention and management.
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