Synonym |
GRF (1-29) amide |
Species |
Human |
Protein Accession |
NA |
Purity |
≥ 98% |
Endotoxin Level |
< 1.0 EU per μg |
Biological Activity |
NA |
Expression System |
NA |
Fusion Tag |
NA |
Predicted Molecular Mass |
3297.8 Da |
Formulation |
Supplied as a lyophilized powder |
Reconstitution |
Reconstitute in water to a concentration of 0.1-1.0 mg/ml |
Storage & Stability |
Store lyophilized product at -20°C. Reconstituted product is stable for up to 3 months at -20°C
|
FAQ
What is Acetyl-(D-Phe2)-GRF (1-29) amide (human) and how does it function within the
body?
Acetyl-(D-Phe2)-GRF (1-29) amide is a synthetic analogue of the naturally occurring Growth
Hormone-Releasing Factor (GRF), designed for its heightened stability and potential efficacy. The
modification in the peptide chain, specifically the substitution at the second position with
D-Phenylalanine, is intended to enhance its biological activity and resistance to enzymatic degradation.
This compound mimics the action of endogenous GRF, which is a key player in the endocrine system,
primarily responsible for stimulating the pituitary gland to secrete growth hormone (GH). GH is crucial
for a variety of bodily functions, including growth, cell repair, and metabolism.
GRF binds to
specific receptors on the pituitary gland, triggering a cascade of intracellular signals that result in
the release of growth hormone into the bloodstream. Once secreted, GH exerts its effects directly as
well as indirectly through the stimulation of Insulin-like Growth Factor 1 (IGF-1) production in the
liver and other tissues. These effects encompass promoting growth in children and adolescents and
regulating body composition, muscle and bone growth, sugar and fat metabolism, and possibly heart
function in adults. By acting as a GRF analogue, Acetyl-(D-Phe2)-GRF (1-29) amide can play a significant
role in research focused on understanding and potentially enhancing these physiological
processes.
The stability and potency of this peptide make it a valuable tool in both therapeutic
research and understanding the intricacies of the hormonal regulation of growth and metabolism. Its
potential applications are numerous, including studies aimed at addressing conditions associated with GH
deficiency or excess, as well as understanding age-related changes in hormonal balance. However, the use
of such compounds should be approached with comprehensive research and conducted under appropriate
conditions to ensure safety and efficacy.
What are the potential applications or benefits of
using Acetyl-(D-Phe2)-GRF (1-29) amide in scientific research?
The allure of Acetyl-(D-Phe2)-GRF
(1-29) amide for scientific research lies in its potential to unravel complex physiological processes
and contribute toward advancements in therapeutic interventions. As a potent analogue of Growth
Hormone-Releasing Factor (GRF), one of its primary benefits is serving as a model to study the endocrine
regulation of growth hormone (GH) secretion. Researchers can exploit this compound to gain a deeper
understanding of how GH influences growth, metabolism, and cellular repair, paving the way for novel
insights into managing conditions arising from GH imbalances.
One significant avenue of research
is examining GH deficiency, both congenital and acquired, which is associated with myriad health
challenges such as reduced muscle mass, increased body fat, and diminished quality of life. Researchers
utilize this analogue to explore potential pathways for stimulating GH release, offering hope for
improved management or treatment options. Similarly, research into excessive GH production, which leads
to conditions such as acromegaly, can benefit from understanding GRF-related pathways, providing
opportunities to develop interventions that could mitigate these effects.
Metabolic studies also
constitute a significant area where Acetyl-(D-Phe2)-GRF (1-29) amide is invaluable. The peptide’s role
in regulating insulin sensitivity and lipid metabolism renders it a potent tool for understanding
metabolic disorders like obesity, type 2 diabetes, and dyslipidemia. Investigations into how GH and
subsequently IGF-1 influence carbohydrate and fat metabolism can unlock new therapeutic strategies aimed
at ameliorating these widespread conditions.
Furthermore, aging research stands to gain
considerably from studies employing this analogue. Given the natural decline in GH levels with age,
understanding how synthetic GRF analogues modulate hormonal pathways can inform anti-aging therapies
focused on improving bone density, muscle mass, and cognitive function in the elderly. Such insights are
crucial, considering the increasing global aging population.
Lastly, the peptide’s ability to
promote cellular repair and regeneration opens another frontier in tissue engineering and regenerative
medicine. Researchers can delve into GH's potential to enhance wound healing or support recovery after
surgical procedures, potentially revolutionizing postoperative care or strategies for treating chronic
wounds.
What are the potential side effects or risks associated with Acetyl-(D-Phe2)-GRF (1-29)
amide in experimental settings?
While Acetyl-(D-Phe2)-GRF (1-29) amide holds promising utility in
research, it is imperative to consider the potential side effects or risks associated with its use in
experimental or clinical settings. Like any hormonal analogue, this compound can affect various bodily
systems, necessitating a cautious approach to its application in research models.
A potential
risk of using GRF analogues is the overstimulation of growth hormone (GH) release, which, if
unregulated, can lead to conditions associated with excessive GH, such as acromegaly. This condition is
characterized by abnormal growth of bones and tissues, leading to a plethora of complications, including
joint pain, cardiovascular issues, and insulin resistance. Researchers must balance achieving desired
stimulation levels while avoiding excessive hormone release that could mimic such pathological
states.
Another consideration is the body's metabolic response to increased GH or IGF-1 levels.
Enhanced GH activity can influence carbohydrate and lipid metabolism, raising concerns about insulin
sensitivity alterations, glucose intolerance, or dyslipidemia. In experimental settings, researchers
must monitor these metabolic parameters to ensure comprehensive data collection on the peptide's safety
profile.
Immunogenicity is another aspect to be wary of, particularly because the introduction of
synthetic analogues can sometimes elicit immune responses. While Acetyl-(D-Phe2)-GRF (1-29) amide is
engineered for human biological systems, research involving different species or in varied experimental
conditions should account for potential immune reactions that might skew results or cause unintended
effects.
Moreover, the stability and breakdown of the peptide in biological systems must be
considered. Degradation products can have unforeseen interactions or effects that differ from the
intended outcomes. Researchers must employ rigorous verification and monitoring protocols to understand
these dynamics within the system being studied.
It is also essential to consider ethical
implications, particularly when translating findings from bench research to potential human
applications. Data regarding the long-term effects of sustained GH elevation, especially through
exogenous means, remain incomplete, urging a conservative approach to any clinical
extrapolation.
To distill these considerations, the research involving Acetyl-(D-Phe2)-GRF (1-29)
amide should be conducted with meticulous setup and consistent monitoring. Control measures should be in
place to mitigate these risks while collecting comprehensive data that could inform future applications
and enhance our understanding of this potent peptide's benefits and limitations.
How does
Acetyl-(D-Phe2)-GRF (1-29) amide compare to other growth hormone-releasing hormone
analogues?
Acetyl-(D-Phe2)-GRF (1-29) amide stands out among other growth hormone-releasing
hormone (GHRH) analogues due to its unique structural modification, aimed at enhancing stability and
biological activity. The insertion of D-Phenylalanine at the second position in the peptide chain is a
deliberate design feature to increase the compound's resistance to enzymatic degradation, a common
challenge with peptide-based agents. This property potentially affords the peptide a longer half-life
and sustained action, making it a compelling choice for research where prolonged GH stimulation is under
study.
In comparing this analogue to others, several key differentiators emerge. Traditional GHRH
peptides may be rapidly degraded in vivo, necessitating frequent dosing or complex formulations to
maintain their biological effects. Acetyl-(D-Phe2)-GRF (1-29) amide's enhanced stability allows
researchers more flexibility in experimental design, potentially reducing the need for repetitive
administrations and thus minimizing disruption to the studied system.
Furthermore, the potency of
Acetyl-(D-Phe2)-GRF (1-29) amide is often a focus of comparison. The specific modifications in this
analogue are tailored to optimize its binding affinity and subsequent activation of the GHRH receptor on
pituitary somatotropes. This heightened receptor interaction can yield more pronounced GH release in
research settings, a feature beneficial for studies aiming to explore maximal hormonal responses or
therapeutic potentials.
Another crucial comparison lies in the specificity of action. By
carefully engineering the peptide sequence, researchers can enhance functional specificity, potentially
reducing off-target effects that could complicate data interpretation. In this regard,
Acetyl-(D-Phe2)-GRF (1-29) amide allows for more precise studies often required in preclinical models
aiming to delineate discrete hormonal pathways.
However, it is also pertinent to consider each
analogue's context within the broader scope of research. Different GHRH analogues may be preferred based
on particular research goals, availability, and cost considerations. Each possesses attributes that
might be more aligned with certain study designs or specific physiological
questions.
Acetyl-(D-Phe2)-GRF (1-29) amide's role within this competitive landscape emphasizes
the innovation and tailored approach required to address the dynamic challenges of hormonal research.
Its distinct profile exemplifies how targeted modifications can yield significant advantages, offering a
valuable tool for advancing our understanding of growth regulation and its clinical
applications.
What precautions should researchers consider when handling and analyzing
Acetyl-(D-Phe2)-GRF (1-29) amide in the laboratory?
Working with Acetyl-(D-Phe2)-GRF (1-29) amide
in the laboratory demands certain precautions to ensure both the integrity of the research and the
safety of the personnel involved. As with any potent biological agent, adhering to appropriate handling
and analytical procedures is essential for obtaining reliable results while minimizing risk
exposure.
Firstly, understanding the compound's molecular characteristics and stability is
crucial. Acetyl-(D-Phe2)-GRF (1-29) amide, like many peptides, may be sensitive to environmental
conditions such as temperature, pH, and light. It is important to store the peptide according to its
specification, often at low temperatures to preserve its integrity until its use. Laboratories should
ensure they have the capability to store such reagents appropriately, including facilities to minimize
temperature fluctuations and contamination risk.
When handling the peptide, researchers should
use personal protective equipment (PPE), including gloves, lab coats, and eye protection, to prevent
direct skin contact, which could be a vector for unintended exposure. Though this compound is tailored
for compatibility with human biological systems, it's critical to mitigate any direct contact until
comprehensive safety assessments, reflecting its nuanced biological activity, have been
conducted.
Researchers should also adopt stringent quality control measures throughout the
peptide's lifespan in the laboratory. This includes verifying the purity of the peptide upon receipt,
often through techniques such as high-performance liquid chromatography (HPLC) or mass spectrometry, to
confirm that it meets experimental requirements. Such assessments should be routine, given that small
deviations could impact experimental outcomes significantly.
In addition, accurate dosing and
administration protocols must be established, considering the peptide's potency. Calibration of
equipment and validation of dosing techniques can prevent errors that may affect both safety and data
validity. Researchers should maintain detailed documentation on the preparation and utilization of
solutions, ensuring all aspects of experimental design are carefully tracked.
Furthermore,
disposal protocols for unused peptide and related laboratory waste are paramount. Given the biological
activity of such compounds, it’s crucial to follow institutional and regulatory guidelines for disposal,
ensuring that waste does not pose a risk to the environment or public health.
By adhering to
these precautions, researchers can foster a safe and effective experimental environment, maximizing the
potential insights Acetyl-(D-Phe2)-GRF (1-29) amide can offer into growth and metabolic regulation.