Synonym |
Bradykinin (1-5) |
Species |
Human |
Protein Accession |
P01023 |
Purity |
Greater than 95% |
Endotoxin Level |
Less than 1 EU/µg |
Biological Activity |
Not specified |
Expression System |
Chemical synthesis |
Fusion Tag |
None |
Predicted Molecular Mass |
556.66 Da |
Formulation |
Lyophilized from a 0.2 µm filtered solution in 10 mM HCl |
Reconstitution |
Reconstitute in water to a concentration of 0.1-1.0 mg/ml |
Storage & Stability |
Store at -20°C. Aliquot and store at -20°C to -80°C for long term. |
FAQ
What is Bradykinin (1-5) and how does it function in the human body?
Bradykinin (1-5) is a
peptide fragment derived from the kinin-kallikrein system, which plays a crucial role in various
physiological processes, including inflammation, blood pressure regulation, and pain modulation. This
system involves the production of bradykinin, a potent vasodilator, which means it helps to widen blood
vessels and thus, contributes to lowering blood pressure. However, bradykinin can also be broken down
into smaller peptide fragments, one of which is Bradykinin (1-5). This particular fragment has been the
subject of extensive biochemical research due to its implications in various cardiovascular and
inflammatory processes.
The most well-noted function of Bradykinin (1-5) is its involvement in
the modulation of inflammatory responses. It is known to have lesser potency compared to its full-length
parent peptide, but it retains some vasodilatory effects which can influence tissue permeability. This
change in permeability can affect the migration of immune cells to sites of injury or infection, thereby
playing a role in the body’s defense mechanisms.
Bradykinin (1-5) is also studied for its ability
to interact with specific receptors on cell surfaces. These interactions can trigger signaling pathways
that influence cellular activities. Unlike the full-length bradykinin, which primarily affects the B2
receptor, Bradykinin (1-5) might engage different receptors, leading to alternative cellular outcomes.
This property suggests that Bradykinin (1-5) could fine-tune responses rather than just triggering them,
pointing towards a more regulatory role in inflammation and pain management systems.
Another
intriguing aspect of Bradykinin (1-5) is its potential role in the cardiovascular system, affecting
processes like angiogenesis, the formation of new blood vessels from pre-existing ones. This action
could be critical in wound healing and the response to cardiovascular injuries. In addition, its
influence on blood pressure regulation, through mild vasodilation, suggests it could play a
supplementary role in the pharmacological management of hypertension.
Biochemically, the study of
Bradykinin (1-5) involves understanding its metabolism, receptor interactions, and the downstream
signaling processes that it mediates. Consequently, research on this peptide could lead to innovative
therapeutic strategies, aiming to mitigate pathological inflammatory responses or cardiovascular
conditions. As research progresses, new insights into its specific actions and potential clinical
applications continue to emerge, signifying its importance in physiological regulation and as a target
for drug development.
What are the potential therapeutic benefits of Bradykinin (1-5) in medical
treatment?
Bradykinin (1-5) has garnered attention for its potential therapeutic applications,
particularly in the treatment of inflammatory conditions and cardiovascular diseases. Its role in
regulating various physiological processes makes it an attractive candidate for drug development in
several medical fields. One of the most promising areas of application is in the modulation of
inflammatory responses. Since inflammation is a common postoperative complication and a characteristic
of various chronic diseases such as arthritis, therapies targeting inflammation can greatly enhance
patient outcomes. Bradykinin (1-5) could serve as a new target for designing drugs that either suppress
or modulate the inappropriate inflammatory responses, potentially leading to symptom reduction and
improved quality of life for patients.
Moreover, its ability to induce vasodilation and influence
blood vessel formation makes Bradykinin (1-5) a candidate for treating cardiovascular issues. It might
aid in managing high blood pressure, which is a risk factor for strokes, heart attacks, and other
conditions. By modulating blood flow and pressure, this peptide could be a part of combination therapies
aimed at achieving better cardiovascular health. Its subtle regulatory effects on blood vessels might
also support tissue repair and regeneration, a useful property for facilitating quicker recoveries from
heart or vascular surgeries.
Bradykinin (1-5) also has potential neuroprotective effects, given
its involvement in pain modulation pathways. Chronic pain management is a complex field with limited
options, and new therapeutic agents are constantly in demand. By targeting the specific pathways
involved in pain perception and modulation, Bradykinin (1-5) could serve as a basis for developing new
analgesics that offer pain relief while minimizing side effects.
Its broader role in cellular
signaling and receptor activity also hints at the possibility of employing it in targeted therapies for
cancer or other proliferative disorders. Therapies based on Bradykinin (1-5) might selectively influence
tumor vascularization or immune cell recruitment to tumor sites, opening novel avenues for cancer
treatment.
In conclusion, while research into the therapeutic benefits of Bradykinin (1-5) is
still ongoing, it is evident that this peptide has significant potential in medical treatment. From
inflammatory diseases and cardiovascular health to neuroprotection and possible cancer therapy, the
applications are diverse and promising. As scientific understanding grows, clinical trials and further
research will determine its efficacy and safety in these fields, potentially leading to new, innovative
treatment options.
How does Bradykinin (1-5) compare to other bradykinin fragments in terms of
biological activity?
When comparing Bradykinin (1-5) to other bradykinin fragments concerning
biological activity, it's essential to consider how these peptides derive from the same parent molecule
but exhibit distinct properties and functions. Bradykinin, the precursor to these fragments, is renowned
for its ability to modulate physiological responses such as vasodilation, pain, and inflammation. Upon
enzymatic cleavage, bradykinin generates fragments, each possessing unique bioactive profiles that
contribute differently to homeostasis and pathological states.
Bradykinin (1-5) specifically,
tends to represent a more moderate activity profile compared to its precursor and some other fragments.
In essence, while the full-length bradykinin (1-9) strongly targets B2 receptors to elicit rapid
physiological responses, Bradykinin (1-5) does not interact as dominantly with those receptor subtypes,
which results in more nuanced and potentially regulatory effects. This characteristic makes it an
intriguing candidate for further research aimed at fine-tuning physiological responses with minimal
systemic disruption.
Other fragments such as Bradykinin (1-7) or (1-8) may exhibit stronger or
different affinities to a broader spectrum of receptor sites. This wider interaction profile can lead to
diverse effects ranging from enhanced vasodilation to more vigorous pain modulation. As such, the
potency and the target specificity of these fragments can vary significantly, impacting their potential
utility in therapeutic contexts.
The unique aspect of Bradykinin (1-5) is its subtle yet
impactful role in modulating inflammation, vascular activities, and possibly contributing to
angiogenesis—features that are not as pronounced in some other bradykinin fragments. It may not induce
the same degree of acute physiological reactions as its parent or longer fragments, lending itself to
applications where controlled modulation is beneficial rather than sweeping systemic
change.
Moreover, the metabolic stability of Bradykinin (1-5) also sets it apart. Some fragments
undergo rapid degradation, which limits their therapeutic utility. However, Bradykinin (1-5)’s relative
stability could facilitate its persistence in circulation long enough to exert desired effects, which is
critical in developing effective therapy models.
Thus, in the realm of peptides derived from the
kinin system, Bradykinin (1-5) occupies a distinctive niche. Its biological activities, while less
potent than the full bradykinin molecule, make it a promising candidate for interventions requiring
subtle modulation. Its unique interaction paradigm offers new possibilities where soft yet specific
alteration of physiological conditions is desirable, achieving therapeutic goals with precision and
potentially fewer side effects.
Are there any known adverse effects associated with Bradykinin
(1-5)?
With any biological agent, including Bradykinin (1-5), understanding its safety profile,
including any potential adverse effects, is essential for evaluating its clinical applicability.
Generally, since Bradykinin (1-5) is a naturally occurring peptide fragment derived from bradykinin, its
safety considerations are more benign compared to synthetic drugs or agents not typically present in the
body. However, due to its role in influencing inflammatory and cardiovascular processes, there are
potential areas of concern that warrant attention in therapeutic experimentation and clinical
trials.
The primary area of concern when discussing potential adverse effects revolves around its
vasodilatory action. While beneficial for lowering blood pressure and increasing blood flow to specific
tissues, unintended systemic vasodilation might result in hypotension, where blood pressure drops to
levels that can cause dizziness, fainting, or even shock in extreme cases. Therefore, controlled
administration and monitoring are crucial, particularly in individuals with pre-existing conditions that
predispose them to blood pressure irregularities.
Furthermore, because Bradykinin (1-5) is
involved in inflammatory pathways, there exists a theoretical risk of exacerbating conditions
characterized by excessive inflammation if not appropriately modulated. This possibility would be
particularly worth noting in subjects with autoimmune disorders or chronic inflammatory diseases. For
instance, while moderate inflammation aids in healing and defense mechanisms, an unchecked increase
could contribute to tissue damage or exacerbate symptoms of chronic inflammatory diseases.
Skin
reactions or localized irritation may pose another potential adverse effect, especially if Bradykinin
(1-5) formulations are administered topically or injected. A hypersensitivity reaction could lead to
rash, erythema, or even localized swelling. Such reactions are relatively rare and typically mild, yet
they warrant precautionary measures during initial exposures.
The peptide’s interaction with
various receptors could also yield unknown effects until fully understood through extensive
pharmacological studies. Key to this process would be identifying any off-target activities that might
result in undesirable side effects or influence critical biochemical pathways meant to be untouched by
its therapeutic action.
Moreover, the long-term effects of sustained Bradykinin (1-5) exposure
are not yet entirely clear. Chronic exposure could potentially lead to tolerance or alteration in
endogenous signaling pathways, emphasizing the importance of understanding the broader context of its
activity.
Collectively, while Bradykinin (1-5) poses several hypothetical adverse effects,
ongoing research and clinical trials remain vital to elucidate these risks further. By characterizing
these aspects carefully, scientific advancements will maximize its therapeutic potential while
maintaining safety.
What current research exists on Bradykinin (1-5) in disease
management?
Research into the role of Bradykinin (1-5) in disease management is expansive and
growing as scientists uncover more about its properties and potential applications across a spectrum of
medical conditions. This small peptide shows promising regulatory effects on inflammation and vascular
function, leading to scientific investigations into its role in managing inflammatory diseases,
cardiovascular conditions, and even contributing to advances in cancer therapy.
One significant
area of research focuses on its anti-inflammatory potential due to its involvement in the
kinin-kallikrein system. Research has been directed towards harnessing its possible suppressive effects
on unwanted inflammation. Dysfunctional inflammatory responses are central to diseases such as
rheumatoid arthritis, inflammatory bowel disease, and other autoimmune conditions. As such, the
modulation of these harmful responses through agents like Bradykinin (1-5) could offer new therapeutic
pathways. Studies involving cellular models suggest that Bradykinin (1-5) may temper inflammatory
responses by altering cytokine production, which are critical mediators in the inflammation cascade.
Although more in vivo studies and clinical trials are necessary, these promising initial results
indicate a potential role in managing chronic inflammatory diseases.
Exploration is also underway
concerning the peptide's cardiovascular benefits. By promoting vasodilation, Bradykinin (1-5) could
contribute to managing hypertension, a critical risk factor for strokes and heart disease. Researchers
are actively investigating whether it can be integrated into current therapeutic regimens or if it
offers novel pathways for treatment which could lead to more effective blood pressure management
strategies. Its angiogenic capabilities, or the ability to promote the formation of new blood vessels,
position Bradykinin (1-5) as a candidate for improving wound healing and potentially aiding in recovery
from ischemic events like heart attacks.
Within the realm of cancer research, the modulation of
blood vessel growth and inflammation could also imply roles in tumorigenesis and metastasis. Studies are
evaluating how Bradykinin (1-5) may influence tumor microenvironments, potentially offering a new avenue
for reducing tumor growth or enhancing the transport of drugs directly to the tumor site. While this
application is still in nascent stages, the peptide’s natural presence in the body suggests it could
sidestep some side effects associated with more aggressive cancer therapies.
Lastly, there is
developing interest in how Bradykinin (1-5) may impact neuroinflammatory conditions and pain modulation.
Research is investigating its ability to affect pain perception pathways and how it might assist in
neuroprotection, which could be pivotal in diseases like multiple sclerosis or neuropathic pain
syndromes.
Overall, Bradykinin (1-5) is at the forefront of research that seeks to innovate
disease management strategies. While ongoing research continues to unfold new possibilities, more
extensive studies and clinical trials are imperative for cementing its role in therapeutic landscapes of
the future.