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IGF-1 DES

IGF Axis & Muscle
DES(1-3)IGF-1Des IGF-1

Overview

IGF-1 DES, also known as DES(1-3)IGF-1 or Des IGF-1, is a truncated variant of Insulin-like Growth Factor 1 (IGF-1), lacking the first three amino acids of the IGF-1 sequence. This modification results in a peptide that is approximately 67 amino acids long. IGF-1 DES is synthesized through recombinant DNA technology, allowing for the production of this peptide in laboratory settings. Its structural alteration enhances its biological activity compared to the full-length IGF-1. Researchers have primarily focused on IGF-1 DES in the context of muscle growth and repair, as well as its role in the IGF axis. Studies have shown that IGF-1 DES can stimulate muscle hypertrophy and regeneration, making it of interest in muscle-wasting conditions. Additionally, it has been investigated for its potential effects on glucose metabolism and cellular proliferation. The mechanism of action of IGF-1 DES involves binding to the IGF-1 receptor with higher affinity than the full-length IGF-1, leading to enhanced activation of downstream signaling pathways such as the PI3K/Akt pathway. This results in increased protein synthesis and cellular growth. Pharmacokinetically, IGF-1 DES has a shorter half-life than IGF-1, with researchers noting rapid degradation in the bloodstream. Its bioavailability varies by administration route, with subcutaneous and intramuscular injections being common in research settings. Current research on IGF-1 DES is ongoing, with studies exploring its therapeutic potential and safety profile. However, it is not approved for medical use by major regulatory agencies, and its use is primarily restricted to research contexts.

Mechanism of Action

IGF-1 DES exerts its effects by binding to the IGF-1 receptor, initiating a cascade of intracellular signaling through the PI3K/Akt pathway. This activation promotes protein synthesis and cellular growth, contributing to its anabolic effects on muscle tissue.

Half-Life

IntranasalNot applicable
OralPoor bioavailability

IGF-1 DES is rapidly degraded in the bloodstream, limiting its half-life.

Storage

Lyophilized

Stable for 2+ years at -20°C, 12 months at 4°C

Reconstituted

Use within 14 days when refrigerated at 4°C

Avoid

Avoid repeated freeze-thaw cycles, direct light

Solvent

Bacteriostatic water or sterile saline recommended

Solubility

IGF-1 DES is soluble in water and commonly used solvents like acetonitrile and DMSO.

Legal Status

🇩🇪DE

Not approved as a medicinal product. Not a controlled substance. Sale as research chemical is a legal grey area.

🇺🇸US

Not approved by the FDA for medical use. Not scheduled by the DEA.

🇦🇺AU

Not approved by the TGA for therapeutic use.

🇬🇧UK

Not approved by the MHRA for medical use.

Legal status information is provided for general reference only and may not reflect the most current regulatory changes. Always verify with official government sources before making any decisions.

10 Research Publications

Vitamin D and benign prostatic hyperplasia -- a review.

Review

The Canadian journal of urology · 2013

Researchers reviewed studies on the relationship between vitamin D and benign prostatic hyperplasia (BPH), a common condition affecting older men. They observed that higher vitamin D levels may be linked to a reduced prevalence of BPH and a decrease in prostate size.

  • Researchers found that vitamin D may inhibit certain pathways involved in prostate cell growth, potentially reducing BPH symptoms.
  • The review indicated that increased vitamin D intake is associated with a lower prevalence of BPH among men.
  • No negative side effects were reported from higher vitamin D intake in the studies reviewed.
PubMed

Enforced epithelial expression of IGF-1 causes hyperplastic prostate growth while negative selection is requisite for spontaneous metastogenesis.

Animal

Oncogene · 2008

Researchers studied the effects of a specific form of insulin-like growth factor-1 (IGF-1) on prostate health in mice. They found that while increased IGF-1 led to abnormal growth in prostate cells, it also hindered the progression to cancer. Additionally, the study indicated that a lack of IGF-1 action may be necessary for the development of advanced cancer and metastasis.

  • Increased IGF-1 caused abnormal growth in prostate cells but did not lead to cancer within a year.
  • Crossbreeding with a prostate cancer model delayed tumor progression and spread in younger mice.
  • Older mice showed widespread metastasis, but the specific IGF-1 variant was not found in advanced tumors.
PubMed

Functional characterization of des-IGF-1 action at excitatory synapses in the CA1 region of rat hippocampus.

Animal

Journal of neurophysiology · 2005

Researchers studied the effects of a specific form of insulin-like growth factor-1 (des-IGF-1) on brain function in young rats. They found that des-IGF-1 significantly increased synaptic transmission in a brain region important for learning and memory, suggesting it may play a role in cognitive improvements.

  • Researchers observed a 40% increase in synaptic transmission in the hippocampus after applying des-IGF-1.
  • The enhancement in synaptic activity was linked to a specific type of receptor (AMPA) and involved certain cellular signaling pathways.
  • These findings may help explain how long-term increases in IGF-1 levels can benefit cognitive function in older animals.
PubMed

Des(1-3)IGF-1 treatment normalizes type 1 IGF receptor and phospho-Akt (Thr 308) immunoreactivity in predegenerative retina of diabetic rats.

Animal

International journal of experimental diabesity research · 2003

Researchers observed that an insulin-like growth factor (IGF)-1 analog could prevent early biochemical changes in the retinas of diabetic rats, which are associated with the progression of diabetic eye disease. Despite ongoing high blood sugar levels, the treatment reduced abnormal protein accumulations in the retina.

  • Type 1 IGF receptor levels increased significantly in the retinas of diabetic rats compared to healthy controls.
  • Phospho-Akt levels, which are linked to cell survival, were also found to be much higher in diabetic rat retinas.
  • Treatment with the IGF-1 analog reduced these abnormal protein levels in the retinas of diabetic rats.
PubMed

Differential effects of des IGF-1 on Erks, AKT-1 and P70 S6K activation in mouse skeletal and cardiac muscle.

Animal

Molecular and cellular biochemistry · 2002

Researchers studied the effects of a substance called des IGF-I on muscle activation in mice. They found that while des IGF-I did not change insulin or IGF-I levels, it significantly reduced blood sugar levels and activated specific pathways in skeletal and cardiac muscles differently.

  • Des IGF-I reduced plasma glucose levels by about 50%.
  • It increased the activation of a protein called Akt-1 in both skeletal and cardiac muscles.
  • Skeletal muscle showed increased activation of p70 S6K, while cardiac muscle did not.
PubMed

Insulin-like growth factor (IGF) binding protein-3 inhibits type 1 IGF receptor activation independently of its IGF binding affinity.

Unknown

Endocrinology · 2001

Researchers found that a protein called IGFBP-3 can inhibit the activation of a specific receptor involved in cell signaling, known as the type 1 IGF receptor, without directly binding to it. This study highlights a unique regulatory mechanism that IGFBP-3 employs, which does not affect other related receptors, such as the insulin receptor.

  • IGFBP-3 significantly reduces the activation of the type 1 IGF receptor in breast cancer cells.
  • The inhibitory effect of IGFBP-3 is specific to the IGF receptor and does not impact the insulin receptor.
  • IGFBP-3's ability to modulate IGF signaling occurs independently of its binding to IGF.
PubMed

Interactions of IGF-1 with the blood-brain barrier in vivo and in situ.

Human

Neuroendocrinology · 2000

Researchers studied how insulin-like growth factor-1 (IGF-1) crosses the blood-brain barrier (BBB) and its behavior in the brain and spinal cord. They found that IGF-1 can enter the brain quickly and remains intact for a short period, suggesting a specific transport system at the BBB that regulates its availability to the central nervous system.

  • Researchers observed that IGF-1 has a half-life of 4.5 minutes in blood and can enter the brain and spinal cord effectively after intravenous injection.
  • The influx rate of IGF-1 into the brain was measured at 0.4 microl/g x min, indicating a significant transport mechanism.
  • The study found that the presence of nonradiolabeled IGF-1 enhances the influx of IGF-1 into the brain when injected, but not during direct brain perfusion.
PubMed

The role of the insulin-like growth factor system in the developing brain.

Review

Hormone research · 1998

Researchers found that insulin-like growth factors (IGFs) are crucial for brain growth and development, particularly in the olfactory bulb. The study observed that IGF-1 can help protect brain cells from damage after injury, while specific binding proteins play an important role in delivering IGFs to their targets. Overall, the IGF system shows promise for supporting brain health and recovery.

  • IGF-1 and its binding proteins are highly active in the developing brain, especially in the olfactory bulb.
  • IGF-1 helps protect neurons from cell death after injury, enhancing their survival.
  • Binding proteins are essential for effectively transporting IGFs to their receptors, influencing brain cell responses.
PubMed

The effects of insulin-like growth factor (IGF)-1, IGF-2, and des-IGF-1 on neuronal loss after hypoxic-ischemic brain injury in adult rats: evidence for a role for IGF binding proteins.

Animal

Endocrinology · 1996

Researchers studied the effects of insulin-like growth factors on brain injury in rats. They found that IGF-1 reduced neuronal loss after a brain injury, while IGF-2 appeared to increase neuronal loss and counteracted the protective effects of IGF-1.

  • IGF-1 significantly reduced neuronal loss in various brain regions after injury.
  • IGF-2 was found to increase neuronal loss in certain areas of the brain.
  • The presence of IGF binding proteins may influence the protective effects of IGF-1.
PubMed

Insulin-like growth factor (IGF)-binding proteins inhibit the biological activities of IGF-1 and IGF-2 but not des-(1-3)-IGF-1.

In Vitro

The Biochemical journal · 1989

Researchers studied how certain proteins, known as IGF-binding proteins, affect the actions of insulin-like growth factors IGF-1 and IGF-2. They found that these binding proteins can inhibit the growth-promoting effects of IGF-1 and IGF-2 but do not affect a variant called des-(1-3)-IGF-1.

  • Researchers found that a binding protein from bovine kidney significantly reduced the ability of IGF-2 to stimulate cell growth and protein production.
  • The study observed that des-(1-3)-IGF-1 was not influenced by the binding proteins, indicating it remains more active than IGF-1 and IGF-2.
  • Researchers noted that the effectiveness of IGF-1 and IGF-2 is inversely related to their binding to these proteins, suggesting that less binding leads to greater biological activity.
PubMed

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This page is for informational and research purposes only. All information is based on published scientific literature. Nothing on this page constitutes medical advice or replaces consultation with a qualified healthcare professional.