Semaglutide (GLP-1) – Lyophilized
Semaglutide (GLP-1) – Lyophilized
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Semaglutide, a synthetic glucagon-like peptide-1 (GLP-1) analog, represents a significant advancement in the field of metabolic health, particularly in diabetes management and weight control. Semaglutide is researched to enhance insulin production, lower blood sugar levels, and preserve pancreatic beta cells while potentially influencing appetite and gastric emptying.
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Peptide Product Usage
PEPTIDE PRODUCTS ARE INTENDED AS A RESEARCH CHEMICAL ONLY.
This designation allows the use of research chemicals strictly for in vitro testing and laboratory experimentation only. All product information available on this website is for educational purposes only. This product should only be handled by licensed, qualified professionals. This product is not a drug, food, or cosmetic and may not be misbranded, misused or mislabled as a drug, food or cosmetic.
Semaglutide (GLP-1) – Lyophilized
Introduction to Semaglutide
Semaglutide, a synthetic glucagon-like peptide-1 (GLP-1) analog, represents a significant advancement in the field of metabolic health, particularly in diabetes management and weight control. This peptide is designed to enhance insulin production, lower blood sugar levels, and preserve pancreatic beta cells while potentially influencing appetite and gastric emptying.
Understanding Semaglutide
- Mechanism of Action: As a GLP-1 receptor agonist, semaglutide works by binding to GLP-1 receptors on pancreatic beta cells, stimulating insulin secretion, and reducing glucagon secretion. This action helps regulate blood glucose levels post-meal.
Semaglutide and Incretin Effect
- Incretin Hormones: Incretins are hormones released by the gastrointestinal tract in response to food intake, aiding in decreasing blood glucose levels. Semaglutide contributes to incretin hormone production, enhancing the body's natural glucose-lowering mechanisms.
Semaglutide and Pancreatic Beta Cells
- Cellular Protection: Research involving non-obese diabetic mice models suggests that Semaglutide may promote the growth of pancreatic beta cells and prevent their apoptosis, thereby maintaining optimal glucose levels in the body.
Semaglutide and Appetite Regulation
- Gastric Motility: Semaglutide may delay gastric emptying, contributing to a feeling of fullness and reduced appetite. This effect has been observed in animal research models.
Research on Semaglutide
Neurological Potential
- Cognitive Enhancement: GLP-1 and its receptors are expressed in brain cells. Studies indicate that GLP-1 receptor agonists like Semaglutide may improve cognitive abilities and offer neuroprotective effects, potentially preventing neuronal injury and enhancing learning.
Cardiovascular Implications
- Cardiac Function: GLP-1 receptors are present in the cardiovascular system. Activation of these receptors by Semaglutide may help maintain cardiac function and optimal blood pressure and reduce the risk of cardiac hypertrophy and heart attack.
- Post-Myocardial Infarction Recovery: Semaglutide may improve glucose uptake in heart muscles, potentially aiding in heart muscle function post-myocardial infarction recovery.
Conclusion
Semaglutide is a promising peptide in metabolic health, offering potential benefits in diabetes management, appetite control, and weight loss. Its neurological and cardiovascular health implications further underscore its significance in medical research. While the current understanding of Semaglutide is substantial, ongoing research is crucial to elucidate its therapeutic potential and safety profile fully.
References:
- Mahapatra MK, Karuppasamy M, Sahoo BM. Semaglutide is a glucagon like peptide-1 receptor agonist with cardiovascular benefits for the management of type 2 diabetes. Rev Endocr Metab Disord. 2022 Jun;23(3):521-539. doi: 10.1007/s11154-021-09699-1. Epub 2022 Jan 7. PMID: 34993760; PMCID: PMC8736331. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8736331/
- Knudsen LB, Lau J. The Discovery and Development of Liraglutide and Semaglutide. Front Endocrinol (Lausanne). 2019 Apr 12;10:155. doi: 10.3389/fendo.2019.00155. PMID: 31031702; PMCID: PMC6474072. https://pubmed.ncbi.nlm.nih.gov/31031702/
- Ahmann AJ, Capehorn M, Charpentier G, Dotta F, Henkel E, Lingvay I, Holst AG, Annett MP, Aroda VR. Efficacy and Safety of Once-Weekly Semaglutide Versus Exenatide ER in Subjects With Type 2 Diabetes (SUSTAIN 3): A 56-Week, Open-Label, Randomized Clinical Trial. Diabetes Care. 2018 Feb;41(2):258-266. doi: 10.2337/dc17-0417. Epub 2017 Dec 15. PMID: 29246950. https://pubmed.ncbi.nlm.nih.gov/29246950/
- Christou GA, Katsiki N, Blundell J, Fruhbeck G, Kiortsis DN. Semaglutide as a promising antiobesity drug. Obes Rev. 2019 Jun;20(6):805-815. doi: 10.1111/obr.12839. Epub 2019 Feb 15. PMID: 30768766. https://pubmed.ncbi.nlm.nih.gov/30768766/
- National Center for Biotechnology Information (2022). PubChem Compound Summary for CID 56843331, Semaglutide.
- Yang Z, Chen M, Carter JD, Nunemaker CS, Garmey JC, Kimble SD, Nadler JL. Combined treatment with lisofylline and exendin-4 reverses autoimmune diabetes. Biochem Biophys Res Commun. 2006 Jun 9;344(3):1017-22. doi: 10.1016/j.bbrc.2006.03.177. Epub 2006 Apr 5. PMID: 16643856. https://pubmed.ncbi.nlm.nih.gov/16643856/</>
- Blonde L, Klein EJ, Han J, Zhang B, Mac SM, Poon TH, Taylor KL, Trautmann ME, Kim DD, Kendall DM. Interim analysis of the effects of exenatide treatment on A1C, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with type 2 diabetes. Diabetes Obes Metab. 2006 Jul;8(4):436-47. doi: 10.1111/j.1463-1326.2006.00602.x. PMID: 16776751. https://pubmed.ncbi.nlm.nih.gov/16776751/
- During MJ, Cao L, Zuzga DS, Francis JS, Fitzsimons HL, Jiao X, Bland RJ, Klugmann M, Banks WA, Drucker DJ, Haile CN. The glucagon-like peptide-1 receptor is involved in learning and neuroprotection. Nat Med. 2003 Sep;9(9):1173-9. doi: 10.1038/nm919. Epub 2003 Aug 17. PMID: 12925848. https://pubmed.ncbi.nlm.nih.gov/12925848/
- Gros R, You X, Baggio LL, Kabir MG, Sadi AM, Mungrue IN, Parker TG, Huang Q, Drucker DJ, Husain M. Cardiac function in mice lacking the glucagon-like peptide-1 receptor. Endocrinology. 2003 Jun;144(6):2242-52. doi: 10.1210/en.2003-0007. PMID: 12746281. https://pubmed.ncbi.nlm.nih.gov/12746281/