All U Health offers the latest cutting-edge pharmaceutical grade peptides under the direct care & safety from our medical team. All the peptides that we offer are from registered pharmacies and are pharmaceutical grade (NOT RESEACH ONLY) peptides that have been tested and have stability studies done on them. The medical team specializes in educating and building a plan to use peptides as the regenerative therapy for our own internal processes.
Peptides are short strains of amino acids and make up larger proteins you may be familiar with like collagen. While some peptides are naturally occurring, scientists have created certain peptides to enhance our bodies natural processes and help treat issues we may have. In short, peptides can often be the key to triggering responses in the body to improve our health and appearance.
While our bodies do naturally produce peptides, the production of peptides in individuals can vary greatly and we generally see a decline in our body’s production of peptides as we age. This is where peptide therapy comes in to play. Peptide therapy is the use of peptides in treatment to direct cells to perform the function specific to the peptide being used. Since our bodies naturally produce many kinds of peptides, there are many different types of peptide therapies, all of which are used to trigger a specific function within the body.
Tirzepatide is the latest weight loss peptide that at therapeutic doses, acts on centers in the brain & suppresses appetite. This peptide focuses on both weight & fat loss by working in two different paths. Used in conjunction with diet & exercise, Tirzepatide helps patients adhere to a reduced-calorie diet, enhancing the weight loss process. Approved in March 2022 by the FDA called Mounjaro™ as an adjunct to diet & exercise to improve glycemic control in adults with type 2 diabetes mellitus, Tirzepatide is a dual glucose-dependent insulinotropic polypeptide (GIP) & glucagon-like peptide-1 (GLP-1) receptor agonist (RA). This means it works by imitating not one, but two unique incretin hormones produced by the human body. It works by stimulating GLP-1 production in the body, which helps the body produce more insulin when needed. GIP has been shown to decrease food intake & increase energy expenditure therefore resulting in weight reductions & when combined with GLP-1 receptor agonism, may result in greater effects on markers of metabolic dysregulation such as body weight, glucose, & lipids.
Semaglutide is a Glucagon-like peptide-1 (GLP-1) produced by the gut. It is commercially called Wegovy & Ozempic. It increases insulin production, a hormone that lowers the blood sugar level while inhibiting glucagon secretion, which is a hormone that raises blood sugar, reduces appetite and energy intake while delaying gastric emptying. It was first developed in 2012 by Novo Nordisk as a longer-acting option to Liraglutide. In 2017 this drug was approved as an anti-diabetic medication used to treat type 2 diabetes and obesity. In June 2021, it got approved for chronic weight management in obese individuals with a (BMI) ≥ 30 kg/m2) or overweight (initial BMI ≥ 27 kg/m2) with at least one weight-related comorbidity.
AOD 9604 is a breakthrough peptide that has shown great results without many of the side effects or risks of other more commonly prescribed fat loss medications. It works by mimicking the way natural Growth Hormone regulates fat metabolism but without the adverse effects on blood sugar or growth that is seen with unmodified Growth Hormone. Like Growth Hormone, AOD 9604 stimulates lipolysis (the breakdown or destruction of fat) and inhibits lipogenesis (the transformation of nonfat food materials into body fat). Recent findings have shown, in addition to its fat loss properties, AOD 9604 processes many other regenerative properties associated with growth hormone. Currently trials are underway to show the application of AOD 9604 in osteoarthritis, hypercholesterolemia, bone, and cartilage repair.
The combination of Ipamorelin and CJC 1295 has been developed because the two can act together on the pituitary and hypothalamus to increase the natural production of growth hormone in the body for improved energy, fitness, and overall health. It is done in this way to maximize the amount of growth hormone being released into your body for therapeutic benefits while acting on two separate families of receptors. This peptide works like Growth Hormone by increasing your IGF1 and GH but it is done by naturally regenerating the body’s ability to produce more growth hormone.
CJC 1295 and Ipamorelin should be taken together in order to maximize the amount of growth being released into your body. This creates a safe and therapeutic anti-aging benefit. Some would even call it the fountain of youth!
Some of the Benefits of CJC 1295/Ipamorelin include, but are not limited to:
• Increased Bone Density
• Strengthens the cardiovascular system
• Increase in muscle mass
• The ability to burn fat
• Increased sex drive
• Improved recovery and repair from Injuries
• Strengthens immune system
• Improves cognition and memory function
• Improves insulin sensitivity
IGF1-LR3 is a breakthrough peptide that has shown great results without many of the side effects or risks of other more commonly prescribed fat loss medications. IGF-1 LR3 inhibits the movement of glucose into the body’s cells which facilitates fat burning and the use of fat in the body for the production of energy. Its effects last most of the day and have made it a preferred variant by a majority of patients and physicians. When IGF-1 LR3 is active in the body, it functions differently in different types of tissues. For instance, in muscle tissue, it makes the muscle more sensitive to insulin’s effects, such as a reduction in fat storage.
A great thing about Ibutamoren is that it increases growth hormone levels with little or no increase in other hormones, such as cortisol. Cortisol suppresses the immune system, reduces wound healing, and impairs learning and memory, and it is usually not good to have this hormone elevated. In addition, this peptide has shown to increase IGF-1 levels for up to 24 hours with a single oral dose.
MOTS-c is a peptide encoded as a sORF in the mtDNA that is metabolically and developmentally regulated, which has endocrine-like effects on muscle metabolism, insulin sensitivity, and weight regulation. For this reason, it establishes its role as a member of a new class of mitochondrial signals. Benefits of MOTS-c include decreased insulin resistance, better transport of sugars to muscle cells, fat loss, increased energy, greater resistance to metabolic stress and improved health and lifespan.
BPC, body protection compound, promotes a response to tendon and ligament injury, BPC-157 accelerates healing by increasing type 1 collagen in these tissues. BPC-157 is cytoprotective and thus helps maintain the mucosal lining of the GI tract. As an anti-inflammatory, it aids in the protection and healing of inflamed intestinal tissues. BPC-157 also aids in tissue damage repair by increasing blood flow to damaged tissues.
Additionally, BPC-157 acts as a neuroprotective by modulating serotonin and dopamine production in the brain.
Thymosin Beta-4 is a protein which consists of 43 amino acids. TB-500 is a synthetic fraction of the protein thymosin beta-4. The main purpose of this peptide is to promote healing. The healing effects of TB-500 have been observed in tendons, ligaments, muscle, skin, heart, and eyes. Thymosin beta-4 is naturally produced in higher concentration where tissue has been damaged. This peptide is also a very potent anti-inflammatory agent.
T-cells come in two forms: killer and helper cells. Killer T-cells are responsible for hunting down and destroying our body’s own cells that are cancerous or infected with bacteria or viruses. TA1 is thought to modulate the immune system by augmenting T-cell function. TA1 may affect thymocytes by stimulating their differentiation or by converting them to active T-cells.
TA1 is in Phase III trials for the treatment of hepatitis C and in Phase II trials for hepatitis B. Additional possible indications are malignant melanoma, hepatocellular carcinoma, drug-resistant tuberculosis, and Di George’s syndrome as well as any chronic cancer or viral disease. Some physicians are using thymosin for chronic fatigue and Lyme disease as well.
Semax act as Melanocortin Stimulating Hormone-like peptides within the brain to initiate wide ranging effects related to brain activity and fitness. Semax has been prescribed for anxiety, memory improvement, ischemic events, stroke, nerve regeneration, ADHD, opioid withdrawal, and even chronic diseases such as ALS, Parkinson’s Disease, and Alzheimer’s.
Selank is an immune-stimulatory synthetic peptide analog of the natural immunopeptide taftsin, which acts in part by stabilizing the natural peptides in the body that are believed to counteract stress response as well as influence the levels of the neurotransmitters – norepinephrine, dopamine, & serotonin which are widely believed to be involved in motivation, focus, & pleasure. Selank is similar to benzodiazepines, without the unwanted side effects of BZDs including: amnesia, withdrawal, & dependence.
Selank has been shown to enhance cognitive function, reduce anxiety and stress levels, improve mood and sleep, and boost the immune response. By stimulating GABA receptors, Selank may promote relaxation and calmness while reducing tension and restlessness. Additionally, it helps regulate cortisol levels in the body, which are responsible for inducing stress responses. As a result, users can experience improved mental clarity and focus while feeling more relaxed overall. Another benefit of Selank peptide is its potential to promote better sleep quality.
PT-141, also known as bremelanotide, is an innovative new peptide hormone treatment that works for both men and women to improve sexual function. This medication was used to treat pre-menopausal women with hypoactive sexual desire disorder (HSDD), which is defined by a persistent lack of interest in sex, causing stress. PT-141 acts on receptors for a brain-stimulating hormone called melanocortin, which is associated with sexual arousal and appetite in both men and women. Unlike Viagra &, Cialis, and related medications (that only give you the ability to achieve an erection), PT-141 does not act upon the vascular system but directly increases sexual desire via the nervous system.
The therapeutic value of this approach lies in its capacity to encourage the formation of new functional synaptic connections among existing neurons, encourage the replacement of damaged and lost neurons from available neural stem cell populations, and facilitate cerebral blood flow and neuroprotection. Such treatment outcomes would benefit patients afflicted with attention deficit and possibly those suffering from other neurodegenerative diseases.