Semaglutide (GLP-1 Analogue) 10mg

Semaglutide is a modified form of the naturally occurring GLP-1 peptide, which plays a key role in regulating blood sugar levels and enhancing insulin secretion. Studies suggest that Semaglutide may also support heart, liver, and lung function while potentially slowing or preventing the progression of Alzheimer’s disease. Research indicates that Semaglutide can significantly reduce appetite by delaying gastric emptying and decreasing intestinal motility. Glucagon-Like Peptide-1 (GLP-1) analogs have been shown to promote insulin release and inhibit glucagon secretion in a glucose-dependent manner.

Semaglutide and GLP-1 Overview

Glucagon-like peptide-1 (GLP-1) is a naturally occurring peptide hormone, consisting of 30-31 amino acids, primarily responsible for regulating blood sugar levels by enhancing insulin secretion. It also supports beta-cell function by promoting insulin gene transcription and has been associated with neurotrophic effects in the brain and central nervous system. In the gastrointestinal system, GLP-1 has been shown to reduce appetite by delaying gastric emptying and slowing intestinal motility. Emerging research suggests its potential effects on various organs, including the heart, fat, muscles, bones, liver, lungs, and kidneys.

GLP-1 research has largely focused on its role in diabetes treatment and appetite regulation, with secondary studies exploring its cardiovascular benefits. More recent investigations, though still in early stages, are examining GLP-1’s potential in slowing neurodegenerative diseases. This area of study is expanding rapidly, particularly in relation to Alzheimer’s disease, as GLP-1 has been shown to help prevent the accumulation of amyloid-beta plaques, a hallmark of the condition.

Semaglutide Structure

Source: PubChem

Sequence: HXEGTFTSDVSSYLEGQAAK-OH.steric diacid-EFIAWLVRGRG

Molecular Formula: C187H291N45059

Molecular Weight: 4113.64 g/mol

PubChem CID: 56843331

CAS Number: 910463-68-2

Synonyms: Semaglutide, Oxempic, Rybelsus, NN9535

Semaglutide and GLP-1 Research

The Incretin Effect of GLP-1

One of the most significant physiological roles of GLP-1 is its contribution to the incretin effect, as described by Dr. Holst. Incretins are metabolic hormones released by the gastrointestinal tract that help lower blood glucose levels. GLP-1, along with glucose-dependent insulinotropic polypeptide (GIP), is one of the two primary hormones responsible for this effect in rodent models. Although GIP circulates at concentrations nearly ten times higher than GLP-1, research suggests that GLP-1 is the more potent regulator, especially in conditions of elevated blood glucose.

A specific GLP-1 receptor has been identified on the surface of pancreatic beta cells, confirming its direct role in stimulating insulin release from the pancreas. Studies have shown that when GLP-1 is combined with sulfonylurea drugs, insulin secretion is enhanced to the point where mild hypoglycemia occurs in up to 40% of subjects. Beyond insulin regulation, increased insulin secretion is associated with several anabolic effects, including enhanced protein synthesis, reduced protein breakdown, and increased amino acid uptake by skeletal muscle.

GLP-1 and Beta Cell Protection

Animal model research suggests that GLP-1 plays a critical role in supporting pancreatic beta cell health by promoting their growth and proliferation. Studies indicate that GLP-1 may also stimulate the differentiation of new beta cells from progenitor cells in the pancreatic duct epithelium while simultaneously inhibiting beta cell apoptosis. Collectively, these effects shift the balance toward beta cell preservation and regeneration, highlighting the potential of GLP-1 in diabetes treatment and pancreatic protection.

One particularly notable study demonstrated that GLP-1 reduces beta cell death induced by elevated levels of inflammatory cytokines. Furthermore, mouse models of type 1 diabetes suggest that GLP-1 can protect pancreatic islet cells from destruction, pointing to its potential role in delaying or preventing the onset of type 1 diabetes.

GLP-1 and Appetite


Studies in mouse models suggest that GLP-1, along with its closely related counterpart, can reduce the drive to eat and suppress food intake when administered directly into the brain. Research indicates that GLP-1 enhances feelings of satiety, helping individuals feel fuller for longer and indirectly reducing hunger.


Recent clinical studies in mice have shown that twice-daily administration of GLP-1 receptor agonists leads to gradual, sustained weight loss. Over time, this weight reduction has been linked to significant improvements in cardiovascular risk factors and a decrease in hemoglobin A1C levels—a key marker of diabetes severity and overall blood sugar control.


Potential Cardiovascular Benefits of GLP-1


Research has shown that GLP-1 receptors are widely distributed throughout the heart, where they play a role in improving cardiac function. GLP-1 has been found to increase heart rate and reduce left ventricular (LV) end-diastolic pressure—a key factor in preventing LV hypertrophy, cardiac remodeling, and heart failure.


Emerging evidence suggests that GLP-1 may also help minimize heart attack damage by enhancing glucose uptake in cardiac muscle cells. This effect provides ischemic heart tissue with essential nutrients, helping maintain function and reduce programmed cell death. Notably, this glucose uptake appears to occur independently of insulin.


Studies in canine models have demonstrated that large infusions of GLP-1 can improve LV performance while reducing systemic vascular resistance. This reduction in vascular resistance can lower blood pressure, decreasing strain on the heart and mitigating long-term consequences such as vascular thickening, LV remodeling, and heart failure. According to Dr. Holst, administration of GLP-1 following cardiac injury has “consistently increased myocardial performance both in experimental animal models and in patients.”


GLP-1 and the Brain

Research suggests that GLP-1 may play a role in enhancing learning and protecting neurons from neurodegenerative diseases such as Alzheimer’s disease. Studies have shown that GLP-1 improves associative and spatial learning in mice and can even mitigate learning deficits in genetically modified mice. Additionally, rats that overexpress GLP-1 receptors in specific brain regions demonstrate significantly enhanced learning and memory compared to control subjects.

Further investigations indicate that GLP-1 may protect neurons from excitotoxic damage, as demonstrated in rat models where it prevented glutamate-induced apoptosis. In cultured cells, GLP-1 has been observed to stimulate neurite outgrowth, a crucial process in neuron development and repair. These findings have led researchers to explore its potential role in halting or even reversing certain neurodegenerative conditions.


Notably, GLP-1 and its analog, exendin-4, have been shown to reduce amyloid-beta levels in mouse models. They also decrease the presence of beta-amyloid precursor protein in neurons. Since amyloid-beta is a major component of the plaques found in Alzheimer’s disease—plaques that correlate with disease severity—scientists are investigating whether reducing amyloid accumulation could help slow cognitive decline. While further research is needed, these findings offer promising insights into possible interventions for mild cognitive impairment and Alzheimer’s progression.


GLP-1 has demonstrated minimal to moderate side effects, low oral bioavailability, and excellent subcutaneous bioavailability in mice. However, dosage scaling from mice to humans is not applicable. GLP-1 available through Next Level Biotech™ is intended solely for educational and scientific research purposes and is not for human consumption. It is available only to licensed researchers.

Referenced Citations

1 "The Physiology of Glucagon-like Peptide 1 | Physiological Reviews." [Online].

2 "Combined treatment with lisofylline and exendin-4 reverses autoimmune diabetes. - PubMed - NCBI." [Online].

3 "The proglucagon-derived peptide, glucagon-like peptide-2, is a neurotransmitter involved in the regulation of food intake. PubMed - NCBI." [Online]

4 "Interim analysis of the effects of exenatide treatment on A1C, weight and cardiovascular risk factors over 82 weeks in 314 overweight patients with... -PubMed - NCBI." [Online].

5 "Cardiac function in mice lacking the glucagon-like peptide-1 receptor. - PubMed -NCBI." [Online].

6 "Glucagon-like Peptide 1 Can Directly Protect the Heart Against Ischemia/Reperfusion Injury | Diabetes." [Online].

7 "Recombinant glucagon-like peptide-1 increases myocardial glucose uptake and improves left ventricular performance in conscious dogs with pacing-ind.... PubMed - NCBI." [Online].

8 "Glucagon-like peptide-1 receptor is involved in learning and neuroprotection. PubMed - NCBI." [Online].

9 "Protection and reversal of excitotoxic neuronal damage by glucagon-like peptide-1 and exendin-4. PubMed - NCBI." [Online].

10 "A new Alzheimer's disease interventive strategy: GLP-1. PubMed - NCBI." [Online]

11 Holst JJ. From the Incretin Concept and the Discovery of GLP-1 to Today's Diabetes Therapy. Front Endocrinol (Lausanne) 2019;10:260. Published 2019 Apr 26. doi: 10.3389/fendo.2019.00260

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6497767/

Information

Peptides

Legal

Support

© Copyright 2025. Next Level Biotech. All Rights Reserved.