Synonym |
Preangiotensinogen (11-14) (human) |
Species |
Human |
Protein Accession |
NA |
Purity |
Greater than 95% by HPLC |
Endotoxin Level |
<1.0 EU per 1 μg of protein |
Biological Activity |
NA |
Expression System |
Chemical Synthesis |
Fusion Tag |
NA |
Predicted Molecular Mass |
NA |
Formulation |
Lyophilized from a 0.2 μm filtered solution in acetonitrile and TFA |
Reconstitution |
Centrifuge the vial prior to opening. Reconstitute in 1% acetic acid to a concentration of
0.1-1.0 mg/ml. |
Storage & Stability |
Store at -20°C. For long term storage, store at -80°C. Avoid repeated freeze-thaw cycles. |
FAQ
What is Preangiotensinogen (11-14) (human), and what role does it play in the human
body?
Preangiotensinogen (11-14) is a peptide derived from the precursor protein angiotensinogen,
which is part of the renin-angiotensin system (RAS) in the body. This intricate hormonal cascade plays a
crucial role in regulating blood pressure and fluid balance. Angiotensinogen itself is produced by the
liver and released into the bloodstream. The sequence (11-14) refers to specific amino acids within the
larger protein, indicating the segment that is biologically active or relevant to the peptide's
function.
The importance of the renin-angiotensin system cannot be overstated, as it is a central
component in the maintenance of cardiovascular homeostasis. The system is activated when a decrease in
blood pressure is detected, prompting the kidneys to release renin. This enzyme cleaves angiotensinogen
to form angiotensin I, which is further converted by the angiotensin-converting enzyme (ACE) to
angiotensin II, a potent vasoconstrictor. Angiotensin II acts on various tissues, resulting in the
contraction of blood vessels, increased blood pressure, and stimulation of aldosterone secretion, which
promotes sodium retention and potassium excretion by the kidneys.
However, the understanding of
the exact role of the shorter segment Preangiotensinogen (11-14) is an area of ongoing research. It is
postulated that these peptides may have distinct biological activities independent of their role in
angiotensin II production, possibly influencing other pathways or acting as neuromodulators. The
exploration of such short peptides derived from larger proteins is critical, as they may offer novel
insights into manipulating the RAS for therapeutic benefits. This could potentially lead to new
interventions for diseases related to blood pressure, heart function, or kidney health. As science
advances, understanding the broader capabilities and impacts of these peptides continues to be a focal
point of cardiovascular and renal research.
How is Preangiotensinogen (11-14) (human) associated
with blood pressure regulation?
Preangiotensinogen (11-14) is closely tied to blood pressure
regulation through its parent molecule, angiotensinogen, which is a fundamental component of the
renin-angiotensin system (RAS). The regulation of blood pressure is an essential physiological process,
and the RAS is a primary regulator of this function. The RAS functions by responding to signals
indicating a drop in blood pressure or plasma sodium concentrations. This prompts the kidneys to produce
and release renin, an enzyme that catalyzes the conversion of angiotensinogen to angiotensin
I.
Subsequently, angiotensin I is converted to angiotensin II by the angiotensin-converting
enzyme (ACE) found predominantly in the pulmonary circulation. Angiotensin II is a potent
vasoconstrictor, meaning it narrows blood vessels, increasing the resistance against which the heart has
to pump, leading to a rise in blood pressure. It also stimulates the secretion of aldosterone from the
adrenal cortex, which increases sodium and water reabsorption in the kidneys, further contributing to
increased blood volume and elevated blood pressure.
Although the primary function of
angiotensinogen is traditionally associated with angiotensin I and II, research into smaller peptide
fragments like Preangiotensinogen (11-14) opens up the possibility of additional regulatory roles. The
bioactivity of these peptide fragments could influence other signaling pathways or exert effects that
modulate blood pressure indirectly. By understanding these mechanisms, research aims to uncover
additional modulatory roles that could offer new therapeutic targets, especially for conditions such as
hypertension where the regulation of blood pressure is compromised. This inquiry highlights the
potential for these peptides to serve as biomarkers or as therapeutic agents designed to fine-tune the
RAS response, providing nuanced intervention strategies that go beyond current medication that primarily
targets ACE or angiotensin II receptors.
What potential therapeutic applications does
Preangiotensinogen (11-14) (human) have in medical science?
The study of Preangiotensinogen
(11-14), derived from angiotensinogen within the renin-angiotensin system (RAS), is opening new avenues
for therapeutic applications. Given the central role of RAS in cardiovascular health, manipulation of
its components presents substantial opportunities for addressing a range of conditions, particularly
those associated with blood pressure abnormalities and fluid imbalances.
Traditional therapeutic
strategies targeting the RAS include the use of ACE inhibitors, angiotensin II receptor blockers (ARBs),
and renin inhibitors. These treatments are primarily aimed at mitigating the effects of angiotensin II
to control hypertension and prevent its long-term cardiovascular consequences. However, with new
evidence suggesting that smaller peptide fragments such as Preangiotensinogen (11-14) may have
biological activities distinct from the larger angiotensin peptides, there is potential for developing
new drugs that could target these specific fragments or their action pathways.
In terms of
therapeutic applications, there is a significant interest in how these peptides might serve as more
targeted treatments that could fine-tune the cardiovascular responses without the broader systemic
impacts observed with current RAS-modulating drugs. For instance, if Preangiotensinogen (11-14) or its
analogs could be shown to influence vasodilation or vasoconstriction in a more controlled manner, they
could offer a means of regulating blood pressure with potentially fewer side
effects.
Furthermore, understanding the implications of these peptides extends beyond
hypertension to other RAS-related diseases such as heart failure, chronic kidney disease, and
potentially metabolic disorders influenced by the cardiovascular system. There is also speculation about
the peptides playing a role in modulating inflammation or immune responses, given the interconnected
nature of these systems with the RAS.
Thus, while direct clinical applications of
Preangiotensinogen (11-14) and related peptides are still in exploratory stages, their potential is
significant. By contributing to the understanding of peptide-specific functionality and its systemic
impacts, these studies could lead to more sophisticated approaches to disease management, tailored
treatment options, and enhanced patient outcomes, particularly for those with complex cardiovascular
profiles. This represents a growing frontier in precision medicine, focusing on the interplay of peptide
functions and broader physiological processes.
How is research involving Preangiotensinogen
(11-14) (human) conducted, and what are some challenges faced?
Research involving
Preangiotensinogen (11-14) is part of a broader scientific inquiry into the components of the
renin-angiotensin system (RAS). This research is conducted through a variety of methodologies, each
designed to explore the potential functions and effects of this specific peptide fragment within the
body's complex regulatory networks. The process typically begins with in vitro studies, where the
peptide is examined in controlled laboratory conditions for its biochemical properties and interactions.
These studies are critical for understanding the peptide's structure, receptor binding capabilities, and
potential biological activities.
Following in vitro exploration, in vivo studies—often utilizing
animal models—are vital for assessing the physiological and pharmacological impacts of
Preangiotensinogen (11-14). These models help scientists observe the peptide's effects on blood
pressure, vascular tone, and its interaction with other components of the RAS, which is necessary for
determining its therapeutic potential and safety profile. Translational research efforts may then move
towards early human trials, where the focus shifts to safety, tolerability, and initial observations of
efficacy in patients.
However, there are significant challenges in this line of research. One
major challenge is the complexity of the RAS itself, a system with numerous interacting components and
feedback loops. Isolating the effects of Preangiotensinogen (11-14) from other peptides and hormones
within the system can be difficult. Additionally, the physiological effects observed in animal models
may not always directly translate to humans due to species-specific differences in cardiovascular and
metabolic regulation.
Another challenge lies in the synthesis and stability of such small peptide
fragments. Peptides can be metabolically unstable and subject to rapid degradation in the body, which
makes delivering an effective dose to the intended site of action challenging. Advancements in peptide
delivery systems, such as the use of encapsulation techniques or peptide analogs with enhanced
stability, are being developed to overcome these issues.
Moreover, ethical and regulatory
considerations also present hurdles, especially as research moves into human trials. Ensuring that
studies adhere to strict ethical guidelines and obtaining the necessary approvals from regulatory bodies
can be a lengthy and complex process.
Despite these challenges, the research into
Preangiotensinogen (11-14) and similar peptides is crucial, as the insights gained hold promise for new,
targeted therapies that could revolutionize the treatment of cardiovascular and renal diseases. The
continued dedication to overcoming these obstacles reflects the scientific community's commitment to
harnessing the potential of these peptides for patient benefit.
What are some current findings or
emerging research trends involving Preangiotensinogen (11-14) (human)?
Recent research involving
Preangiotensinogen (11-14) has illuminated several intriguing areas that could redefine our
understanding of the renin-angiotensin system (RAS) and its associated physiological pathways. As the
scientific community delves deeper into the peptide's specific role, several emerging trends and
findings have started to take shape, which could have significant implications for medical
science.
One of the emerging trends is the study of Preangiotensinogen (11-14) as a modulator of
vascular function beyond its traditional role in angiotensin II generation. Researchers are
investigating how this peptide might influence endothelial function and contribute to vascular
relaxation or contraction in ways that are distinct from the effects of angiotensin II. Understanding
these effects is pivotal as it could lead to new therapeutic targets for treating hypertension and
related cardiovascular disorders.
Additionally, there has been a growing interest in the
peptide's potential role as a neuromodulator. The link between RAS and the central nervous system is
being explored, with findings suggesting that angiotensinogen-derived peptides might interact with
pathways that regulate sodium appetite, thirst, and even behavioral responses. This line of research is
opening new avenues in understanding how blood pressure regulation might intersect with neurological
function and behavior.
In the realm of technology, advances in peptide synthesis and analytical
techniques are facilitating more sophisticated studies of Preangiotensinogen (11-14). Cutting-edge mass
spectrometry and bioinformatics tools are allowing for detailed analysis of peptide interactions within
complex biological matrices, which is crucial for identifying specific targets and pathways
involved.
Another hot topic within emerging research is the exploration of peptide stability and
delivery. Modifications to enhance the stability of such peptides in vivo can help in the creation of
new, more effective therapeutic agents. Innovative delivery systems, such as nanoparticles and peptide
analogs, are being designed to improve bioavailability and target specificity, which would make
potential treatments more efficient and with fewer side effects.
Moreover, personalized medicine
is becoming a significant focus in this research area. The genetic and phenotypic variation in
angiotensinogen production and processing among individuals could lead to personalized therapeutic
approaches based on one's specific cardiovascular and metabolic needs. Understanding how
Preangiotensinogen (11-14) interacts with other genetic factors could pave the way for precision
treatments tailored to individual patient profiles.
Collectively, these trends and findings are
advancing the potential for novel interventions that harness the intricate balance of peptide
interactions in the renin-angiotensin system. As this area of research continues to evolve, the promise
of Preangiotensinogen (11-14) as a key player in cardiovascular and neurological health becomes
increasingly apparent, offering hope for more effective and personalized healthcare solutions.