Synonym |
AM (16-31) |
Species |
Human, Pig |
Protein Accession |
P35318 |
Purity |
Greater than 95% |
Endotoxin Level |
Less than 1 EU/μg |
Biological Activity |
Not specified |
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
~2.9 kDa |
Formulation |
Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA |
Reconstitution |
Centrifuge vial before opening. Reconstitute in 10mM Acetic Acid to a concentration of 0.1-1.0
mg/ml |
Storage & Stability |
Store at -20°C. Aliquot and store at -20°C for long term. Avoid repeated freeze/thaw cycles |
FAQ
What is Adrenomedullin (16-31) and what are its primary functions in biological systems?
Adrenomedullin (16-31) is a peptide fragment derived from the larger adrenomedullin protein, which
is an important biological molecule involved in numerous physiological processes, including
vasodilation, immune response modulation, and osmoregulation. The peptide sequence of Adrenomedullin
(16-31) specifically corresponds to a segment of the adrenomedullin protein and is characterized by its
capacity to mimic some of the functions of the full-length peptide. Adrenomedullin, as a whole, is
widely recognized for its potent vasodilatory properties, contributing to blood pressure regulation and
cardiovascular homeostasis. It is released by various tissues in the human body, such as the adrenal
medulla, endothelial cells, and cardiac tissue, in response to physiological demands. The peptide
facilitates an increase in blood flow by relaxing vascular smooth muscles and plays an integral role in
the broader regulatory mechanisms that control vascular tone. Beyond its vascular effects,
adrenomedullin also acts as an anti-inflammatory mediator. It exerts this effect by modulating immune
cell activity and cytokine production, thereby acting as a protective agent in inflammatory conditions.
Adrenomedullin (16-31), as a fragment, may have distinct and possibly enhanced or specialized activities
compared to the whole protein. Particularly, this fragment can be significant in research focused on
specific pathways or cellular environments, allowing scientists to investigate targeted therapeutic
potentials, whether concerning cardiovascular diseases, inflammatory disorders, or cellular protection
mechanisms. Furthermore, due to its evolutionary conservation across species, such as in humans and
pigs, it provides a versatile model for comparative studies, which can advance our understanding of its
functions in different organisms. This conservation suggests foundational roles in both species,
offering insights into its significance in evolutionarily preserved physiological processes.
How
does Adrenomedullin (16-31) influence cardiovascular function, and what implications could this have for
medical research?
Adrenomedullin (16-31) plays a significant role in cardiovascular function through
its potent vasodilatory effects, which are paramount for regulating blood vessel tone and blood
pressure. This peptide fragment contributes to the relaxation of vascular smooth muscle cells, leading
to the widening of blood vessels, a reduction in peripheral resistance, and consequently, lowered blood
pressure. By modulating these processes, Adrenomedullin (16-31) can influence overall cardiovascular
homeostasis, enhancing blood flow to organs and tissues, which is crucial for maintaining oxygen and
nutrient supply to the body. This effect is particularly beneficial in conditions where blood
circulation is compromised, such as in hypertension, heart failure, and ischemic diseases. The actions
of Adrenomedullin (16-31) have several implications for medical research, especially when exploring
novel therapeutic avenues for cardiovascular diseases. The precise dissection of its effects offers
opportunities to develop new pharmacological agents that might harness its vasodilatory properties to
manage blood pressure more effectively or provide myocardial protection. Research into Adrenomedullin
(16-31) could lead to therapies that supplement or mimic its activity, particularly in patients with
elevated cardiovascular risk. This fragment, by mitigating inflammatory processes and promoting vascular
health, could be pivotal in slowing the progression of atherosclerosis, a major antecedent to heart
attacks and strokes. Additionally, its role in the heart suggests it might aid in myocardial repair and
adaptation, especially following cardiac injury. Another critical aspect for research is the potential
of Adrenomedullin (16-31) to operate in synergy with existing cardiovascular treatments, possibly
enhancing their efficacy or reducing side effects. Understanding these interactions may pave the way for
combination therapies that offer more comprehensive management of cardiovascular conditions. As research
delves deeper into these mechanisms, Adrenomedullin (16-31) holds promise not only as a therapeutic
target but also as a biomarker for diagnostic purposes, where its levels might indicate cardiovascular
health or disease states, providing clinicians with crucial information to tailor individualized
treatment plans.
Can Adrenomedullin (16-31) be used to modulate the immune response, and if so,
what are its mechanisms of action in immunological contexts?
Adrenomedullin (16-31) can indeed
modulate the immune response, making it an important focus of research in immunology. This peptide
fragment is involved in regulating inflammatory processes, suggesting its potential as a therapeutic
tool in various inflammatory and autoimmune disorders. Its immunomodulatory actions are achieved through
several mechanisms. Firstly, Adrenomedullin (16-31) exerts an inhibitory effect on pro-inflammatory
cytokine production. Cytokines are signaling molecules that mediate and regulate immunity and
inflammation. By reducing the secretion of inflammatory cytokines such as TNF-alpha, IL-6, and IL-1beta
by immune cells, the peptide can attenuate inflammatory responses that are typically upregulated in
acute or chronic inflammatory conditions. This action can help limit tissue damage associated with
excessive inflammation. Furthermore, Adrenomedullin (16-31) influences immune cell behavior, including
that of macrophages and dendritic cells, which play critical roles as antigen-presenting cells and
modulators of immune responses. It promotes a regulatory macrophage phenotype, which is associated with
tissue repair and inflammation resolution, as opposed to a pro-inflammatory phenotype. This shift can
lead to a more balanced immune response, avoiding the detrimental effects of chronic inflammation.
Additionally, Adrenomedullin (16-31) affects the maturation and function of dendritic cells, which are
pivotal in initiating and regulating the adaptive immune response. By modulating dendritic cell
activity, it can influence T cell responses and help maintain immune tolerance, which is crucial in
preventing autoimmune reactions. The peptide also enhances the production of other immunoregulatory
mediators, such as IL-10, an anti-inflammatory cytokine that plays a key role in controlling
inflammation and autoimmunity. This suggests that Adrenomedullin (16-31) could be leveraged as a
treatment to promote immune homeostasis in diseases like rheumatoid arthritis, lupus, and inflammatory
bowel disease, where immune dysregulation is a primary concern. The potential to modulate the immune
response in such a targeted way presents an exciting avenue for the development of novel treatments
aimed at reducing the burden of inflammatory diseases while minimizing side effects often associated
with conventional immunosuppressive therapies.
What potential does Adrenomedullin (16-31) have in
therapeutic applications, and what areas of research are particularly promising?
The therapeutic
potential of Adrenomedullin (16-31) is vast, given its involvement in multiple physiological systems,
notably the cardiovascular and immune systems. This peptide fragment is garnering attention in many
areas of research, with particular interest in its possible applications in managing cardiovascular
diseases, inflammatory disorders, and metabolic abnormalities. In cardiovascular research,
Adrenomedullin (16-31) is a promising candidate for the development of treatments aimed at managing
hypertension and heart failure due to its vasodilatory effects. By promoting blood vessel relaxation, it
could help to lower blood pressure and improve cardiovascular function in patients with hypertension,
where traditional therapies may be inadequate or cause unwanted side effects. Moreover, its myocardial
protective properties hold potential for reducing ischemic injury and improving outcomes post-myocardial
infarction. Its role in modulating inflammation also suggests potential as a treatment for
cardiovascular inflammation and atherosclerosis, reducing plaque buildup in arteries. In immunological
and inflammatory research, the peptide's capacity to modulate immune responses without broadly
suppressing immunity is particularly attractive for developing therapies for autoimmune diseases and
chronic inflammatory conditions. Treatments that can specifically downregulate harmful inflammation,
while preserving needed immune functions, remain a critical unmet need in this field. In diseases such
as rheumatoid arthritis and inflammatory bowel disease, Adrenomedullin (16-31) might help to control
disease activity and flare-ups by reducing inflammatory cytokine production and promoting immune
homeostasis. Furthermore, metabolic research is beginning to explore Adrenomedullin (16-31) in the
context of glucose metabolism and insulin sensitivity. Some studies suggest that it may impact metabolic
pathways relevant to diabetes, potentially offering an innovative approach to addressing metabolic
syndrome and Type 2 diabetes. Additionally, because of its diverse bioactivities, there is interest in
exploring how Adrenomedullin (16-31) might interact with neural pathways or contribute to
neuroprotection, opening new frontiers in treating neurodegenerative diseases. The potential for using
this peptide fragment in conjunction with other therapies represents another promising research area,
where synergies could lead to more comprehensive treatment strategies with enhanced efficacy and safety
profiles. As such, continued research into the mechanisms, efficacy, and safety of Adrenomedullin
(16-31) will be critical in translating these promising findings into clinical applications.
What
are the challenges and limitations currently facing research into Adrenomedullin (16-31), and how might
these be addressed in future studies?
Research into Adrenomedullin (16-31) faces several challenges
and limitations, which current and future studies need to address to fully realize its therapeutic
potential. One of the primary challenges is the complexity of adrenomedullin's mechanisms of action.
Understanding the specific pathways through which Adrenomedullin (16-31) exerts its effects requires
comprehensive research that disentangles its interactions within diverse biological systems. This
complexity can be challenging when trying to isolate its effects from the complete adrenomedullin
peptide or other interacting pathways in vivo. Advanced techniques such as molecular modeling, along
with transcriptomic and proteomic analyses, may aid in identifying the precise receptors and secondary
messengers involved in its actions. Another limitation is the need for robust preclinical and clinical
data to establish the safety and efficacy of Adrenomedullin (16-31) in potential therapeutic
applications. Most current research is at the in vitro or early animal study stage, necessitating the
development of reliable animal models that mimic human disease to assess the peptide's therapeutic
effects. Bridging the gap from bench to bedside will require carefully designed clinical trials that
evaluate dosage, administration routes, and long-term effects. Additionally, issues surrounding the
pharmacokinetics and bioavailability of peptide therapeutics must be addressed, as peptides often face
challenges with stability, degradation, absorption, and delivery. Innovative drug delivery systems, such
as nanoparticle-based carriers or formulation strategies that enhance peptide stability, could improve
the potential for oral or targeted delivery of Adrenomedullin (16-31). Adaptive designs and
controlled-release mechanisms may offer solutions that increase the peptide's therapeutic window and
efficacy. Intellectual property and regulatory landscapes present further hurdles in translating
findings into clinical use. Navigating these processes will require collaboration between researchers,
industry, and regulatory bodies to expedite the development of therapies that can meet stringent safety
and efficacy standards. Finally, the translation of findings from animal models to human applications
poses inherent challenges, given the potential differences in animal and human physiology. Thus,
comparative studies that use highly relevant models, such as primate studies or advanced human cell
models, can help bridge this gap. Addressing these challenges and limitations will be instrumental in
advancing Adrenomedullin (16-31) from a research subject to a viable therapeutic candidate for various
diseases.