Synonym |
Met-Enk-Arg |
Species |
Human |
Protein Accession |
P01210 |
Purity |
≥ 95% |
Endotoxin Level |
< 1.0 EU per 1 μg of protein |
Biological Activity |
The ED50 for this effect is typically 1-5 nM. |
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
Approximately 5.7 kDa |
Formulation |
Lyophilized from a 0.2 μm filtered solution of 20mM PB, 150mM NaCl, pH 7.0 |
Reconstitution |
Centrifuge the vial prior to opening. Reconstitute in 5-10mM NaOH containing carrier protein
(e.g. BSA) to a concentration of 0.1-1.0 mg/mL. This solution can then be diluted into other
aqueous buffers and stored at 4°C for 1 week or -20°C for future use. |
Storage & Stability |
Store lyophilized protein at -20°C. Aliquot the product after reconstitution to avoid repeated
freezing/thawing cycles. Reconstituted protein can be stored at 4°C for a limited period of
time; it does not show any change after one week at 4°C. |
FAQ
What is Met-Enkephalin-Arg and how does it function in the body?
Met-Enkephalin-Arg is a naturally
occurring peptide, part of the enkephalin family, which is a type of endogenous opioid peptide.
Enkephalins are pentapeptides produced in the central nervous system and adrenal medulla, and they have
been found to bind to opioid receptors in the brain. Met-Enkephalin-Arg is known for its role in
modulating pain and rewarding effects, influencing mood, and regulating various physiological processes.
The peptide primarily interacts with the delta-opioid receptors, which are involved in analgesic
processes, mood regulation, and the reinforcement of reward-driven behaviors. When Met-Enkephalin-Arg
binds to these receptors, it triggers a cascade of biochemical events that lead to the inhibition of
neurotransmitter release, particularly those involved in the transmission of pain signals like Substance
P. This modulation of neurotransmitter release leads to the perception of reduced pain, providing a
natural analgesic effect. Moreover, Met-Enkephalin-Arg, through its interaction with opioid receptors,
influences the dopaminergic system, which plays a critical role in mood regulation and reward
perception. Such interactions have implications for mood disorders, addiction, and pain management. The
significance of Met-Enkephalin-Arg lies in its ability to enhance the body's natural defense against
stress and pain while promoting a sensation of well-being. Additionally, ongoing research is uncovering
its potential therapeutic applications in treating conditions such as chronic pain, depression, and
substance dependency, by exploiting its modulatory effects on specific neurotransmitter systems.
Understanding its mechanism offers insights into creating innovative approaches in improving mental
health and managing pain without the addictive tendencies associated with synthetic opioids.
What
are the potential benefits of Met-Enkephalin-Arg in therapeutic applications?
The potential
therapeutic benefits of Met-Enkephalin-Arg are largely centered around its ability to modulate
analgesia, mood, and immune response through its interaction with the body's opioid receptors. One of
the most prominent benefits is its role in pain management. By binding predominantly to delta-opioid
receptors, it can effectively inhibit the transmission of pain signals and provide significant analgesic
effects without some of the adverse effects associated with traditional opioid medications, such as
respiratory depression or severe dependency issues. This positions Met-Enkephalin-Arg as a viable
candidate for developing pain management therapies, particularly for individuals with chronic pain
conditions that require long-term management strategies. Another notable benefit is its impact on mood
regulation. As Met-Enkephalin-Arg influences the opioid and dopaminergic systems, it could be a crucial
element in developing treatment solutions for mood disorders like depression and anxiety. Research
indicates that it might help in modulating mood by reducing the threshold for neuronal excitation and
mitigating stress response, thus offering a drug-free approach to managing mood disorders. Beyond these,
preliminary studies suggest that Met-Enkephalin-Arg may have immunomodulatory effects, potentially
enhancing immune response and offering therapeutic value in immunocompromised conditions. This paves the
way for exploring innovative treatments for conditions like autoimmune disorders or infections where
boosting the immune response is crucial. Furthermore, its role in mitigating reward-driven behaviors
opens potential avenues in the treatment of addiction, particularly for substances where dependency is
heightened, providing the dual benefits of pain relief and addiction control. Each of these therapeutic
applications not only underscores the versatility of Met-Enkephalin-Arg but also highlights the
importance of continued research into understanding its complete biological impact.
How does
Met-Enkephalin-Arg impact mood and emotional regulation?
Met-Enkephalin-Arg exerts a pronounced
influence on mood and emotional regulation through its complex interactions with the opioid and
dopaminergic systems in the brain. These systems are integral to the regulation of mood, perception of
pleasure, and emotional responses. By binding primarily to delta-opioid receptors, Met-Enkephalin-Arg
modulates neurotransmitter release, which can alter mood states and contribute to an individual's
emotional well-being. Within the central nervous system, the interaction of Met-Enkephalin-Arg with its
receptors can enhance the release of dopamine, a neurotransmitter fundamentally linked to mood and the
reward pathways of the brain. This interaction is crucial because dopamine modulation is associated with
improving mood, reducing anxiety, and creating a sense of reward or pleasure. Increased dopamine levels
can effectively reduce feelings of depression, chronic stress, and anxiety, contributing to an overall
enhancement of mood. Additionally, by reducing the release of neurotransmitters like Substance P, which
are associated with pain and emotional distress, Met-Enkephalin-Arg further aids in decreasing stress
and depressive symptoms. The peptide's impact on mood is also associated with its ability to reduce
neuronal excitability. During periods of stress or anxiety, excitability can increase, leading to
heightened states of emotional distress. Met-Enkephalin-Arg helps in stabilizing this excitability, thus
promoting psychological tranquility and a balanced emotional state. Furthermore, research suggests that
the peptide may have neuroprotective effects, which could contribute to delaying or alleviating mood
disorders. The implications for therapeutic use are immense, as enhancing emotional regulation and
reducing mood disorder symptoms could lead to innovative treatments outshining current pharmaceutical
options that often come with significant side effects. Met-Enkephalin-Arg, with its multifaceted impact
on mood, offers a promising path for new approaches to mental health therapy that are both effective and
more aligned with the body’s natural biochemistry.
How might Met-Enkephalin-Arg contribute to the
management of chronic pain?
Met-Enkephalin-Arg holds significant promise in the management of
chronic pain owing to its ability to naturally modulate pain perception through its interaction with the
endogenous opioid system. Chronic pain, characterized by persistent pain signals within the nervous
system, presents a complex therapeutic challenge, often requiring interventions that effectively
alleviate pain without leading to addiction or severe side effects. Met-Enkephalin-Arg acts as a natural
analgesic by binding to and activating delta-opioid receptors, which are implicated in mediating the
transmission and modulation of pain signals in the central nervous system. This receptor interaction
directly inhibits the release of neurotransmitters that are responsible for conveying pain perception,
thus leading to a natural reduction in pain intensity. Importantly, because Met-Enkephalin-Arg acts
endogenously and targets specific opioid receptors, the risk of adverse side effects common with
synthetic opioids, such as addiction or respiratory depression, is significantly reduced. This makes it
a potentially safer option in pain management strategies. Moreover, Met-Enkephalin-Arg is suggested to
have anti-inflammatory properties, helping to alleviate pain that originates from inflammatory
processes, especially relevant in diseases like arthritis or autoimmune conditions where chronic
inflammation exacerbates pain. By reducing inflammation at the source, Met-Enkephalin-Arg can hinder the
chronic pain cycle, offering relief not just temporarily but as a part of a long-term management plan.
Another compelling aspect of Met-Enkephalin-Arg in chronic pain management is its potential
neuroprotective properties. Chronic pain often involves maladaptive changes within the nervous system,
yet the neuroprotective facets of Met-Enkephalin-Arg might counteract such changes, preserving neuronal
function and mitigating the progression of pain pathways. As research progresses, these properties
highlight the potential of Met-Enkephalin-Arg to be developed into a therapeutic agent that addresses
not only the symptoms of chronic pain but also its underlying neurological basis, presenting a holistic
approach to chronic pain management.
What role does Met-Enkephalin-Arg play in the immune system?
Met-Enkephalin-Arg's role in the immune system is gaining attention for its potential to enhance
immunomodulation, which is crucial in maintaining homeostasis and responding to pathogens. Opioid
peptides like Met-Enkephalin-Arg can influence immune cell function, and their interaction with opioid
receptors extends beyond the central nervous system into the immune system. These interactions suggest
that Met-Enkephalin-Arg can modulate the balance and activity of immune cells, impacting a range of
immune responses. One of the most significant roles of Met-Enkephalin-Arg in the immune system is the
regulation of cytokine production. Cytokines are signaling proteins that mediate and regulate immunity,
inflammation, and hematopoiesis. Met-Enkephalin-Arg can influence the production and release of
cytokines, promoting a balanced immune response that is neither underactive nor overly aggressive. This
regulatory capability is particularly valuable in autoimmune conditions, where an over-responsive immune
system attacks healthy cells, and in chronic inflammatory conditions, where unchecked inflammation
causes tissue damage. Furthermore, Met-Enkephalin-Arg is believed to enhance the activity of natural
killer (NK) cells, which are vital components of the innate immune system responsible for identifying
and destroying infected or malignant cells. By boosting NK cell activity, Met-Enkephalin-Arg could
contribute to the body's ability to manage infections and reduce the risk of tumor development. Its
immunomodulatory role extends to improving overall resistance against infections, emphasizing its
potential in treating immunocompromised states. Additionally, Met-Enkephalin-Arg appears to impact the
adaptive immune system by influencing the balance between T-helper cells, which play a critical role in
orchestrating complex immune responses. By modulating the ratio of different T-helper cell types,
Met-Enkephalin-Arg can indirectly influence how effectively the immune system responds to various
antigens. This presents an exciting prospect for its use in vaccines or therapies designed to manage or
prevent infectious diseases. As research into Met-Enkephalin-Arg continues, its impact on the immune
system signifies promise for future therapeutic strategies that incorporate modulation of both innate
and adaptive immunity.
How does Met-Enkephalin-Arg differ from synthetic opioids in its mode of
action?
Met-Enkephalin-Arg differs from synthetic opioids in several critical ways in terms of its
mode of action, specificity, and resulting physiological effects. At the core, Met-Enkephalin-Arg is a
naturally occurring peptide that is part of the body's endogenous opioid system, whereas synthetic
opioids are artificial compounds designed to mimic the pain-relieving properties of natural opioids.
Met-Enkephalin-Arg primarily interacts with delta-opioid receptors, unlike many synthetic opioids which
often have a high affinity for mu-opioid receptors. The mu-opioid receptors, when activated by synthetic
opioids, are largely responsible for the high levels of pain relief but also the significant side
effects, such as respiratory depression, sedation, and a high potential for addiction. In contrast,
delta-opioid receptors, which Met-Enkephalin-Arg targets, are mainly associated with modulating
emotional responses and alleviating pain without the intense euphoria that leads to addiction. This
selectivity allows Met-Enkephalin-Arg to provide effective analgesia while minimizing the risk of
dependency and side effects frequently observed with synthetic opioids. Another difference lies in the
biological assimilation and metabolism of these compounds. Being a naturally occurring peptide,
Met-Enkephalin-Arg is metabolized by the body’s natural pathways, often resulting in quicker degradation
and fewer long-term systemic effects compared to synthetic opioids which are designed for prolonged
bioavailability and often impose a more significant metabolic load on the body. This rapid
biotransformation leads to a self-limiting mechanism of action, reducing the risk of accumulation and
toxic side effects. Moreover, Met-Enkephalin-Arg's mode of action involves subtle modulation of
neurotransmitter release, achieving analgesic effects through the body’s existing pathways, whereas
synthetic opioids override these systems, leading to a more pronounced suppression of neurotransmitter
release, contributing further to the risk of addiction and tolerance. Hence, Met-Enkephalin-Arg presents
a promising alternative to synthetic opioids in developing new pain management therapies that offer
effective relief while reducing the adverse effects associated with traditional opioid
treatments.
What are the challenges associated with using Met-Enkephalin-Arg in clinical
settings?
Despite the promising therapeutic potential of Met-Enkephalin-Arg, there are several
challenges associated with its use in clinical settings that must be addressed to facilitate its
application as a therapeutic agent. One of the primary challenges lies in its stability and
bioavailability. As a peptide, Met-Enkephalin-Arg is inherently susceptible to rapid degradation by
peptidases in the gastrointestinal tract and serum when administered orally or intravenously. This rapid
breakdown can limit its effectiveness as a therapeutic, necessitating the development of delivery
systems or modified versions of the peptide that can resist enzymatic degradation and maintain
bioactivity for a clinically relevant duration. Another significant challenge is in the specificity of
drug action required to minimize potential side effects. While Met-Enkephalin-Arg primarily targets
delta-opioid receptors, any off-target effects or unanticipated interactions with other physiological
systems could complicate its therapeutic use. Therefore, precise targeting and delivery systems are
essential to ensure that the peptide exerts its intended effects at the required receptor sites without
influencing other systems adversely. Also, understanding the optimal dosage and administration routes is
crucial, yet current data may not provide comprehensive details on long-term pharmacokinetics and
pharmacodynamics in diverse patient populations who might present varied responses based on genetic or
environmental factors. Additionally, large-scale production and purification of peptides remain a
technological and economic hurdle. Producing peptides like Met-Enkephalin-Arg at pharmaceutical-grade
quality in sufficient quantities to meet clinical demands is technically challenging and costly.
Ensuring purity and consistency in peptide production requires advanced manufacturing processes and
rigorous quality control to prevent any contamination or degradation that might occur during synthesis
and storage. Research and development efforts are needed to address these issues before
Met-Enkephalin-Arg can be widely used in a clinical setting. Finally, understanding the full scope of
its beneficial and adverse effects through extensive clinical trials is essential. Extensive human
trials are a significant undertaking, requiring robust study designs to conclusively demonstrate both
efficacy and safety across diverse patient groups. Addressing these challenges is critical to harnessing
Met-Enkephalin-Arg’s full potential in clinical applications, helping to pave the way for its use as a
viable therapeutic option in the future.