Synonym |
Ac-α-MSH (11-13) |
Species |
Human |
Protein Accession |
N/A |
Purity |
≥ 95% |
Endotoxin Level |
< 1.0 EU/µg |
Biological Activity |
N/A |
Expression System |
Chemical synthesis |
Fusion Tag |
Acetyl |
Predicted Molecular Mass |
619.66 Da |
Formulation |
Lyophilized from a 0.1% TFA in H2O |
Reconstitution |
Centrifuge vial before opening. Reconstitute in sterile, non-adhesive polypropylene vial |
Storage & Stability |
Lyophilized product is stable at room temperature for up to 3 weeks. Store reconstituted product
at -20°C |
FAQ
What is Acetyl-α-MSH (11-13), and how does it work?
Acetyl-α-MSH (11-13) is a synthetic peptide
segment derived from the naturally occurring melanocyte-stimulating hormones (MSH), particularly the
short sequence from positions 11 to 13. These hormones are part of the larger class of melanocortins,
peptides involved in a variety of physiological functions such as pigmentation, energy homeostasis, and
appetite regulation. The specific sequence 11-13 refers to a subset of amino acids within the larger
alpha-MSH peptide, and the acetylation of this sequence is believed to enhance certain biological
activities, such as binding affinity and stability.
The way Acetyl-α-MSH (11-13) works is
largely through its interaction with melanocortin receptors, especially MC1R and MC4R, which are
distributed in different tissues throughout the body. Upon binding to these receptors, Acetyl-α-MSH
(11-13) can trigger a cascade of intracellular events that lead to diverse outcomes based on the type of
receptor and tissue involved. For instance, at MC1R located primarily in the skin, this peptide can
stimulate melanogenesis, leading to increased melanin production and thus affecting pigmentation
processes. Meanwhile, interaction with MC4R, which is also expressed in the brain, can influence energy
balance and food intake. The peptide’s precise mechanisms can vary, invoking secondary messengers like
cAMP and activating different signaling pathways depending on the targeted receptor.
The
peptide's ability to predominantly function through these receptor-mediated interactions makes it an
interesting focus for research, with potential applications not only in dermatology but also in areas
such as metabolic functions and even immunomodulation. Scientists are exploring how modifications, such
as acetylation, can be optimized to develop more effective therapeutic agents with minimized side
effects. Given these diverse capabilities, Acetyl-α-MSH (11-13) is a promising candidate for a wide
range of biotechnological and therapeutic applications, although precise outcomes depend significantly
on dosage, method of delivery, and receptor selectivity.
What are the potential benefits of using
Acetyl-α-MSH (11-13)?
Acetyl-α-MSH (11-13) offers a range of potential benefits largely due to
its activity at melanocortin receptors, which play variegated roles in the human body. One of the
primary benefits is its role in skin pigmentation. By interacting with MC1R on melanocytes, it can
stimulate melanin production, thus enhancing pigmentation. This feature not only offers cosmetic
benefits, potentially providing a sunless tanning effect but also serves a protective role, as melanin
can absorb harmful UV radiation. The use of this peptide could be beneficial as a protective agent
against UV-induced damage or in conditions where increased pigmentation is desired, such as in vitiligo
treatment or depigmentation issues.
Beyond skin applications, Acetyl-α-MSH (11-13) could provide
benefits in energy metabolism and weight management. Its action at the MC4R in particular is associated
with the regulation of food intake and energy homeostasis. Studies suggest that stimulation of this
receptor can lead to decreased appetite and increased energy expenditure, which might be leveraged in
developing treatments for obesity or metabolic disorders.
Moreover, there is emerging interest
in its potential anti-inflammatory and immunomodulatory effects. Melanocortins, in general, have been
associated with exerting anti-inflammatory actions, and while the specific effects of the (11-13)
sequence are still under research, there's potential for this peptide to influence inflammatory
pathways. This opens avenues for its possible use in managing inflammatory or autoimmune
conditions.
Furthermore, because melanocortins can affect neurological functions, Acetyl-α-MSH
(11-13) might also impart cognitive or neuroprotective benefits. While preliminary, some research does
focus on the role of melanocortin peptides in neurodegenerative diseases or brain injuries, exploring
their capacity to potentially support neuronal health.
These conceptual benefits mean that
Acetyl-α-MSH (11-13) is under considerable scientific investigation. While promising, it's essential
that these potential applications are backed by rigorous clinical studies to establish safety and
efficacy; thus, it’s mostly being explored in controlled research settings rather than widespread
clinical practice currently.
Are there any risks or side effects associated with Acetyl-α-MSH
(11-13)?
While Acetyl-α-MSH (11-13) holds promise for various therapeutic applications, as with
any bioactive peptide, its use could present certain risks and side effects. Understanding these
potential adversities is crucial for safely harnessing its benefits. The primary area of concern arises
from its interaction with melanocortin receptors, which are involved in multiple physiological
systems.
One immediate concern is the peptide’s effect on pigmentation. While increased melanin
production can be beneficial and desirable in some contexts, it may not be suitable for everyone.
Enhanced pigmentation can lead to hyperpigmentation issues, especially in individuals prone to such
conditions. Additionally, uneven distribution of pigmentation effects could result, depending on where
and how the peptide is administered.
From a systemic standpoint, potential issues could also
arise from its impacts on the central nervous system. Since melanocortin receptors like MC4R are
involved in regulating appetite and energy expenditure, there’s a possibility for unintended effects on
eating behaviors. In theory, overstimulation of these receptors could lead to anorexia or other
appetite-related disorders, although such outcomes would typically depend on dosage and individual
susceptibility.
Furthermore, the peptide’s potential anti-inflammatory effects also need careful
management. While reducing inflammation is often desired, improper or excessive modulation of the immune
response could render a person more susceptible to infections or negatively affect wound healing
processes.
Another aspect to consider is the risk of allergic reactions or hypersensitivity,
which is inherent in any biologically active peptide therapy. The possibility of developing antibodies
against the peptide could also diminish its efficacy over time or lead to adverse immunological
responses.
Importantly, these risks highlight the necessity for controlled use within research
settings where dosages are carefully calibrated. Researchers aim to tailor acetylation and other
modifications to enhance the peptide’s profile for therapeutic use while minimizing its side effects. As
with any investigational compound, extensive clinical trials are essential to evaluate safety
comprehensively. It's worth noting that comprehensive safety data and guidelines should be followed if
Acetyl-α-MSH (11-13) transitions into broader clinical applications from the research-focused interest
it currently garners.
How does Acetyl-α-MSH (11-13) compare to other melanocyte-stimulating
hormones?
Acetyl-α-MSH (11-13) is a distinct yet related derivative within the family of
melanocyte-stimulating hormones, known as melanocortins. Understanding how it compares with other
members of this family involves examining its biochemical uniqueness and functional specificity.
Melanocyte-stimulating hormones such as alpha-MSH, beta-MSH, and gamma-MSH are naturally occurring
peptides that play crucial roles in regulating pigmentation, energy homeostasis, and immune responses by
binding to melanocortin receptors located throughout the body.
The key difference between
Acetyl-α-MSH (11-13) and its larger counterparts lies in its peptide structure and the effect of
acetylation. While alpha-MSH is itself a segment of the larger proopiomelanocortin (POMC) polypeptide
chain, Acetyl-α-MSH (11-13) is a shortened, acetylated form. Acetylation can enhance peptide stability
and receptor binding affinity, potentially offering more potent or prolonged effects compared to
non-acetylated forms.
Functionally, while alpha-MSH (the full-length version) acts broadly across
several melanocortin receptors and has a well-characterized role in skin pigmentation and
anti-inflammatory activity, Acetyl-α-MSH (11-13) might offer a more targeted approach with distinct
biochemical properties. The precise impacts of such peptides can vary based on their receptor
selectivity. For example, some derivatives might show higher affinity for certain receptor subtypes,
influencing pigmentation more than metabolism or vice versa.
In terms of therapeutic exploration,
the specific characteristics of Acetyl-α-MSH (11-13) might offer advantages in areas like receptor
selectivity or bioavailability that could make it preferable in certain settings, such as dermatological
applications where targeted action and minimized systemic activity are desirable. Comparatively,
full-length MSH might be more broadly effective but also more likely to cause systemic
effects.
Overall, while all melanocyte-stimulating hormones share common biological terrains—such
as affecting pigmentation and metabolism—the nuances in their molecular structures mean that
Acetyl-α-MSH (11-13) could potentially be optimized for specific therapeutic functions with distinct
safety and efficacy profiles. The ongoing research seeks to establish these comparisons more robustly,
aiming to tap into benefits that might not be as achievable with the naturally occurring full-length
peptides.
What current research exists on Acetyl-α-MSH (11-13), and what does it focus
on?
Current research on Acetyl-α-MSH (11-13) explores its potential across various biomedical
domains, driven by its activity at melanocortin receptors and the promise of acetylation-enhanced
efficacy. This peptide’s unique ability to modulate pigmentation, energy metabolism, and immune
responses positions it as a subject of interest for several therapeutic applications.
One
prominent focus of research is the dermatological application of Acetyl-α-MSH (11-13), particularly its
potential as a tanning agent or for treating pigmentary disorders like vitiligo. Scientists are
examining how this peptide can effectively increase melanin production with the intent to provide safe
and controlled pigmentation in clinical scenarios. Such studies are significant because they help
establish parameters, such as dosage and delivery methods, optimizing the peptide for desirable cosmetic
outcomes without adverse side effects.
Another active area of research is on its metabolic
effects, especially concerning weight management and appetite regulation. Given its action on MC4R,
studies aim to evaluate the peptide’s influence on energy balance and food intake, which could translate
to novel treatments for obesity or metabolic syndromes. Animal and early phase human trials might assess
changes in metabolic rate, energy expenditure, and appetite following treatment with Acetyl-α-MSH
(11-13), providing insights into its potential clinical utility in metabolic disorders.
Additionally, research is exploring its immunomodulatory properties. There is interest in
understanding how Acetyl-α-MSH (11-13) can modulate inflammatory processes, with animal models often
employed to assess its effectiveness in conditions characterized by excessive inflammation or immune
dysregulation.
The exploration into neurological impacts—potential cognitive or neuroprotective
benefits related to its interaction with brain-expressed melanocortin receptors—is another intriguing
angle. Such studies might investigate the peptide’s effects in neurodegenerative diseases or cognitive
disorders, assessing neuroprotection, synaptic plasticity, or overall brain health
impacts.
Overall, current research is heterogeneous, spanning preclinical trials and some
early-stage clinical investigations. Researchers strive to translate the promising biological mechanisms
observed in vitro and animal models into tangible clinical therapies. However, each application requires
careful evaluation through comprehensive studies to ascertain safety, efficacy, and long-term outcomes.
This expanding body of research aims to unlock therapeutic avenues and refine the application landscape
for Acetyl-α-MSH (11-13) through rigorous scientific inquiry.