Taiy Chemical
δ-MSH
Synonym Delta-MSH
Species Human
Protein Accession POMC
Purity ≥ 95%
Endotoxin Level < 1.0 EU per μg
Biological Activity N/A
Expression System E. coli
Fusion Tag None
Predicted Molecular Mass 3.1 kDa
Formulation Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA
Reconstitution Centrifuge vial before opening. Reconstitute in 10 mM Sodium Phosphate, pH 7.5 to a concentration of 0.1-1.0 mg/ml.
Storage & Stability Store at -20°C upon receipt. Stable for up to 6 months at -20°C.
FAQ
What is δ-MSH, and how does it work in the human body?

δ-MSH, or Delta-Melanocyte Stimulating Hormone, is a peptide hormone that is primarily known for its role in skin pigmentation. It is a member of the melanocortin family, which includes other hormones such as α-MSH and β-MSH. These hormones are products of the proopiomelanocortin (POMC) gene and are involved in various physiological processes. δ-MSH is produced in the pituitary gland and acts on the melanocortin receptors, particularly the MC1R (melanocortin 1 receptor), which is predominantly found in melanocytes, the cells responsible for pigmentation in the skin and hair. By binding to MC1R, δ-MSH stimulates the production of melanin, the pigment that gives skin, hair, and eyes their color. This process is called melanogenesis.

Beyond pigmentation, δ-MSH and its interaction with melanocortin receptors have several other biological implications. Melanocortin receptors are distributed throughout the body, including in the brain, adipose tissue, and immune cells, suggesting that δ-MSH could influence a variety of systems. In addition to influencing pigmentation, δ-MSH has been studied for its potential roles in anti-inflammatory responses, regulation of appetite, and energy homeostasis. Its anti-inflammatory properties arise from its ability to target specific pathways and modulate immune responses, which may help in reducing inflammation associated with certain autoimmune conditions.

Research has also indicated that δ-MSH may be involved in the body's response to stress, as melanocortin peptides are implicated in the stress axis and stress-induced physiological changes. Furthermore, due to the widespread presence of its receptors, δ-MSH may influence the central nervous system, potentially affecting mood and behavior, although the exact mechanisms and implications of these effects require further scientific investigation. Overall, while δ-MSH is traditionally recognized for its role in pigmentation, its multifunctional nature highlights the complexity and interconnectivity of hormonal regulation in the body.

What are the potential therapeutic applications of δ-MSH?

δ-MSH is gaining attention in various research fields due to its broad range of potential therapeutic applications, driven by its ability to interact with melanocortin receptors which are involved in critical physiological processes. One of the most notable avenues of exploration is in the treatment of skin-related conditions. Given its role in stimulating melanin production, δ-MSH is being studied for its potential use in conditions like vitiligo, a disorder characterized by depigmented patches of skin. By enhancing melanin synthesis, δ-MSH could help restore pigmentation in affected individuals, offering a new avenue for treatment beyond traditional methods like phototherapy or topical steroids.

Apart from its dermatological applications, δ-MSH’s influence on inflammation positions it as a candidate for treating inflammatory diseases. In particular, researchers are exploring its utility in managing autoimmune conditions where chronic inflammation is a core issue. By modulating immune responses, δ-MSH might offer a pathway to reduce inflammation without the severe side effects associated with long-term use of conventional anti-inflammatory drugs like corticosteroids.

δ-MSH’s role in regulating appetite and energy homeostasis also presents potential therapeutic applications in tackling obesity and metabolic disorders. The peptide’s effect on appetite suppression could be harnessed to develop treatments that help manage weight by reducing food intake and promoting satiety. Moreover, due to its action on the melanocortin receptors involved in metabolism, δ-MSH could aid in enhancing metabolic rate and thus help manage or prevent obesity, diabetes, and other related metabolic conditions.

Moreover, δ-MSH is of interest in the neurological field due to its potential neuroprotective roles. It might assist in protecting neurons from damage in neurodegenerative diseases like Alzheimer’s and Parkinson’s. While research is in the early stages, the potential for δ-MSH in these areas warrants further investigation, as it could lead to breakthroughs in how such conditions are managed. The hormone's ability to modulate neural pathways could also mean it has potential applications in mental health, particularly in conditions linked with stress and mood regulation.

Is δ-MSH safe for therapeutic use, and what are the potential side effects?

The safety profile of δ-MSH for therapeutic use is a significant consideration that researchers and healthcare professionals are investigating. As of now, δ-MSH is primarily still within the experimental and research phases, especially concerning its application in humans. Initial studies and trials are pivotal in determining both its efficacy and safety margins across different potential therapeutic applications. It's essential to approach any hormone or peptide therapy with a careful understanding of its interactions, potential benefits, and side effects.

In current research and trials, δ-MSH has shown promise with relatively favorable safety indices, particularly when used in controlled environments. However, as with any biologically active peptide, there is potential for side effects, which researchers continue to evaluate. Common concerns when it comes to peptide hormones like δ-MSH include their potential to affect off-target sites due to the wide distribution of receptors across various body systems. This widespread receptor presence means that while δ-MSH might be beneficial for specific conditions, it could also unintentionally affect other systems, leading to side effects.

Potential side effects noted in studies include local reactions at the site of administration, which is common with peptide therapies, and can include redness or swelling. More systemic side effects depend on the area of application, for instance, affecting appetite, which might not be desired in individuals without metabolic disorders. Also, as δ-MSH can influence pigmentation, there could be unintended changes in skin tone, which although generally reversible, may not be desired cosmetically.

Furthermore, the immunomodulatory effects, while beneficial for conditions like autoimmune diseases, could pose a risk if they disturb the normal immune balance, potentially leading to an increased risk of infections or other immune complications. It is critical for complete clinical trials to occur to ascertain the long-term effects and establish firm safety guidelines for δ-MSH’s therapeutic use. These trials would help identify which patient populations would benefit the most from δ-MSH therapy and under what conditions it can be safely administered.

How does δ-MSH compare with other melanocyte stimulating hormones in terms of activity and function?

δ-MSH, like other members of the melanocyte-stimulating hormone family such as α-MSH and β-MSH, plays a crucial role in regulating pigmentation and is involved in several physiological processes through the activation of melanocortin receptors. However, each of these hormones has unique characteristics concerning their activity and function, influenced by their specific binding affinities and receptor distribution. δ-MSH is particularly interesting due to its distinct role among the MSH peptides, partly due to its different receptor binding profiles and its specific physiological outcomes.

Among the MSH peptides, α-MSH is the most studied and known for its potent activity in inducing melanogenesis, primarily through binding to the MC1R on melanocytes. This binding promotes increased melanin production, which is instrumental in pigmentation. α-MSH also has pronounced anti-inflammatory and anorexigenic effects, acting on multiple receptors spread across various body tissues. On the other hand, β-MSH, while also involved in pigmentation, is less potent than α-MSH and has other roles in energy homeostasis and the regulation of the adrenal cortex's activity.

δ-MSH, although sharing similar pathways and receptor interactions, has a different focus of activity. Its affinity for melanocortin receptors varies compared to α- and β-MSH. These differences can lead to varied biological responses, which are a subject of interest in ongoing research. One of the unique aspects of δ-MSH is its involvement in inflammatory processes. It appears to modulate certain inflammatory pathways potentially more effectively than its counterparts, presenting opportunities for targeted therapies where inflammation is a significant clinical problem.

In terms of functional scope, δ-MSH may not stimulate pigmentation as strongly as α-MSH but might offer a more balanced profile concerning its other roles. Researchers are particularly interested in δ-MSH as potentially providing therapeutic benefits with a possibly better side effect profile in applications where broader hormonal activation might lead to side issues. Understanding these differences helps in leveraging the unique properties of δ-MSH for therapeutic applications where other MSH variants might not be as effective or suitable. This comparative analysis continues to evolve, especially as detailed receptor studies and clinical trials shed more light on the subtle nuances of each MSH peptide's action.

What are the challenges in developing δ-MSH-based therapies?

Developing δ-MSH-based therapies presents several challenges that need to be addressed to ensure safe and effective use. Foremost among these challenges is the complexity of the human endocrine and immune systems, where δ-MSH interacts with multiple receptors and pathways. This complexity makes it difficult to predict the outcomes of δ-MSH therapy accurately. Understanding the intricacies of its interactions with various melanocortin receptors is crucial, as these interactions will determine both the efficacy of treatment and the potential side effects. Designing therapies that maximize δ-MSH's beneficial effects while minimizing unintended interactions within the body remains a significant scientific hurdle.

Another core challenge lies in the delivery mechanisms for δ-MSH-based therapies. Peptide-based treatments often face difficulties related to their stability and bioavailability. δ-MSH, being a peptide, is susceptible to degradation by enzymes in the gastrointestinal tract, meaning oral administration is generally ineffectual. Developing an effective delivery system, whether through injectable formats, transdermal, or novel drug delivery technologies, is essential to ensure that δ-MSH is delivered to the sites where it is needed without significant degradation.

Moreover, the regulatory landscape for new peptide therapies, including δ-MSH, adds another layer of complexity. Rigorous testing is required to meet safety standards and regulatory approval, which necessitates significant investment in clinical trials to demonstrate not only efficacy but also long-term safety. Establishing comprehensive trials that assess the therapeutic index, side effects, and pharmacokinetics across diverse patient populations is essential for regulatory approval, demanding substantial time and financial commitments from developing companies.

Finally, there is a need for a deeper understanding of δ-MSH’s broader systemic effects and potential long-term consequences. While much research has identified potential benefits, understanding contraindications and the long-term stability of its effects are crucial. Long-term studies will be paramount in ensuring the viability and safety of δ-MSH-based therapies, as these will inform best practices and guidelines for healthcare providers. Overcoming these challenges requires integrated research efforts, collaboration between academic institutions and pharmaceutical companies, and a concerted effort to advance scientific understanding and technological capabilities.
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