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GLP-1, scientifically referred to as Liraglutide, is a naturally occurring peptide renowned for its ability to promote insulin secretion. Extensive research suggests that this remarkable peptide holds the promise of reducing blood sugar levels and enhancing the overall functionality of vital organs like the heart, liver, and lungs. Given its potential to counteract increases in blood sugar levels, it has become an attractive option for researchers seeking to combine it with MK 677, a compound known to induce such elevations in study subjects.
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GLP-1, or Glucagon-Like Peptide 1, is a naturally occurring peptide with significant relevance in the realm of research. This peptide is highly regarded for its unique properties and potential applications.
Recognized under the brand names Victoza and Saxenda, it acts as an agonist for glucagon-like peptide 1 (GLP-1). In vitro studies have indicated its potential to hinder beta cell apoptosis and stimulate beta cell growth. Additionally, Liraglutide shows promise in retarding gastric emptying, which may contribute to weight loss. [R][R]
The development of Liraglutide involved a strategic modification, replacing lysine with arginine at position 34 within the GLP-1 peptide structure. This innovation was necessary due to GLP-1’s suboptimal pharmacokinetic characteristics. The original peptide boasts a brief half-life of a mere 2 minutes and is rapidly degraded by endogenous enzymes. [R][R]
GLP-1 exerts its effects primarily on the endocrine system, specifically in relation to the regulation of glucose metabolism. It plays a pivotal role in the secretion of insulin, helping to maintain glucose homeostasis. This intricate process involves GLP-1 binding to its receptor, initiating a cascade of events that culminate in enhanced insulin release, suppressed glucagon secretion, and delayed gastric emptying. These actions collectively contribute to the potential reduction of elevated blood sugar levels.
Researchers have been delving into the multifaceted aspects of GLP-1 and its potential applications in various domains of scientific investigation.
One notable benefit of GLP-1 research lies in its implications for diabetes management. GLP-1 has demonstrated the ability to enhance insulin secretion, making it an appealing subject for studies focused on improving diabetes treatment strategies.
In a 52-week placebo-controlled trial, type 2 diabetes patients (ages 10 – 17) were randomly assigned to receive either Liraglutide or placebo. Results from the trial show that Liraglutide, at a dose of up to 1.8 mg per day, was potentially effective in improving glycemic control over the course of the study. [R]
In another study, the effects of Liraglutide treatment on patients with T2D were noted. It was found that 0.6 mg once daily Liraglutide administration potentially improved fasting plasma glucose. This effect was significant after the 1st week and persisted through eight weeks of treatment. [R]
Another promising avenue of research involving GLP-1 is its impact on cardiovascular health. Studies have indicated that GLP-1 may exert beneficial effects on the cardiovascular system, potentially reducing the risk of heart-related complications.
In a mouse model of human heart failure, treatment with Liraglutide improved cardiac function. It also reduced cardiac hypertrophy, decreased myocardial fibrosis, and reduced attenuation of atrial weight. Liraglutide treatment was also shown to decrease lung congestion. [R]
In the realm of liver function, GLP-1 research has unveiled its potential to influence liver health positively. Investigations are ongoing to explore how this peptide might be harnessed to address liver-related conditions.
Numerous clinical trials have unveiled the potential advantages of Liraglutide in the realm of weight management.
In a double-blind clinical trial encompassing 3,731 individuals struggling with obesity, the once-daily administration of Liraglutide demonstrated the potential to reduce body weight and enhance metabolic control. Impressively, 63.2% of the participants achieved a weight loss of at least 5%, with 33.1% experiencing even more substantial reductions exceeding 10% of their initial body weight. [R]
Another study explored the effects of Liraglutide 3.0 mg in 115 patients characterized by an average BMI of 34.8. Remarkably, after four months of treatment, the median body weight witnessed a notable reduction of 9.2%. It is worth mentioning that significant weight loss was observed even among individuals who did not receive the maximum prescribed dose. [R]
Lastly, a phase III trial focused on evaluating the impact of Liraglutide treatment on patients with BMIs ranging from 30 to 40. The results from this investigation underscored the potential of Liraglutide 3.0 mg as a robust agent for weight loss, both in the short term and as a viable option for sustained long-term weight management. [R]
Research has shown that GLP-1 is potentially capable of preventing amyloid beta accumulation. This beta-amyloid precursor protein is the primary component of plaques found in Alzheimer’s disease. Unrelated to that, GLP-1 may promote gene transcription, protecting beta cell insulin stores.
GLP-1, as a naturally occurring peptide, holds promise in various fields of research. From its role in diabetes management and cardiovascular health to potential applications in liver and lung function, ongoing investigations are shedding light on the diverse benefits and implications of this intriguing peptide.
Strength | 30mcg per spray/3mg/10ml |
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