IGF-1 DES Overview
IGF-1 DES (Des(1-3)IGF-I) is a truncated, naturally occurring analogue of Insulin-like Growth Factor-1. This specific variant is characterized by the absence of the first three amino acids—Glycine, Proline, and Glutamic acid—from the N-terminus of the peptide chain. While standard IGF-I is a primary mediator of growth hormone effects, IGF-1 DES is uniquely concentrated in areas requiring rapid cellular adaptation, such as the human brain and bovine colostrum.
The removal of the N-terminal tripeptide grants IGF-1 DES a biological profile that is ten times more potent than its full-length counterpart. This heightened efficacy is attributed to its inability to bind with IGF-I Binding Proteins (IGFBPs), which normally inhibit the peptide’s interaction with its receptors. Consequently, IGF-1 DES remains highly bioavailable for immediate receptor activation. Research currently explores its utility in addressing muscle-wasting conditions, neurological development in autism, and gastrointestinal barrier integrity.
IGF-1 DES Structure
The structure of IGF-1 DES consists of 67 amino acids in a specific sequence that mimics the core of the 70-amino acid IGF-I molecule. By truncating the N-terminus, the molecule gains a more favorable pharmacokinetic profile for crossing biological membranes and avoiding inhibitory protein sequestration.
Molecular Structure Formula: Carbon 319, Hydrogen 495, Nitrogen 91, Oxygen 96, Sulfur 6
IGF-1 DES Research
Potency and Receptor Interaction
In physiological environments, most IGF-I is rendered inactive by binding proteins (IGFBPs). IGF-1 DES lacks the binding site for these proteins, allowing it to remain in a free, active state. Studies in mammalian cell cultures and animal models have confirmed that because IGF-1 DES does not compete with binding proteins, it can stimulate the IGF-1 receptor at much lower concentrations than native IGF-I. This makes it an exceptionally efficient tool for studying hypertrophy and cellular proliferation.
Neurological Applications and Autism Spectrum Disorder
Research into neurodevelopmental disorders has highlighted a correlation between IGF-I deficiency and autism symptoms. Children with autism often exhibit lower concentrations of this peptide during critical stages of brain growth. IGF-1 DES is of particular interest because its modified structure allows it to cross the blood-brain barrier more effectively than full-length IGF-I. In mouse models, the administration of IGF-1 DES has been shown to reverse behavioral deficits, improve spatial memory, and stabilize synaptic transmission.
Research Category
Primary Scientific Finding
Potential Application
Hypertrophy
10x greater potency in muscle cell growth
Muscle wasting diseases
Bioavailability
Zero affinity for IGF-binding proteins
High-efficiency research dosing
Neurobiology
Enhanced synaptic neuron health
Autism, Fragile X Syndrome
Metabolism
Rapid clearance of blood glucose
Type II Diabetes research
Immunology
Stimulation of neutrophils and macrophages
Infectious disease management
Metabolic Health and Glucose Regulation
Experimental data suggests that IGF-1 DES acts as a rapid-acting anti-hyperglycemic agent. In pig studies, it has demonstrated a superior ability to lower blood sugar and improve nitrogen balance compared to standard insulin or IGF-I, even under calorie-restricted conditions. Researchers believe this makes it a strong candidate for studying the management of metabolic disorders where insulin resistance is a factor.
Oncology and Tissue Repair
In cancer research, IGF-1 DES has been observed to induce differentiation in leukemia and colon cancer cells. By forcing these undifferentiated, rapidly dividing cells to become specialized, the peptide effectively halts tumor proliferation. Additionally, in the field of dermatology, IGF-1 DES supports wound healing by stimulating dermal fibroblasts to create the extracellular matrix necessary for tissue closure, even in environments characterized by high inflammation.
Product Storage
IGF-1 DES is highly sensitive to environmental conditions. The lyophilized powder should be stored in a freezer at -20 degrees Celsius for long-term stability. Once the peptide is reconstituted with a sterile diluent, it must be stored in a refrigerator at 2 to 8 degrees Celsius and protected from light. It is recommended to minimize repeated freeze-thaw cycles to maintain biological activity.
Author and Scientific Recognition
Article Author
This material was researched and edited by Dr. Logan, M.D. Dr. Logan holds a doctorate from Case Western Reserve University School of Medicine and a degree in molecular biology.
Scientific Journal Author
Dr. Clemmons is a prominent investigator in the field of endocrinology, specializing in the molecular pathways of growth factors. His research focuses on how IGF-I and its variants promote cellular differentiation and proliferation. He is acknowledged here for his foundational work in the field. Dr. Clemmons has no affiliation with Peptide Sciences and does not endorse the use or sale of this product.
Referenced Citations
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