Synonym |
BNP-45 (rat) |
Species |
Rat |
Protein Accession |
P55045 |
Purity |
Greater than 95% as determined by SDS-PAGE |
Endotoxin Level |
Less than 1 EU/μg |
Biological Activity |
The ED50 for this effect is typically 1-3 ng/mL |
Expression System |
E. coli |
Fusion Tag |
No tag |
Predicted Molecular Mass |
4.5 kDa |
Formulation |
Lyophilized from a 0.2 μm filtered solution of 20 mM citrate, pH 2.0 |
Reconstitution |
Centrifuge the vial prior to opening. Reconstitute in water to a concentration of 0.1-1.0 mg/mL
|
Storage & Stability |
Store at -80°C. Avoid repeated freeze-thaw cycles. |
FAQ
What is Brain Natriuretic Peptide-45 (rat) and what are its primary functions in research?
Brain
Natriuretic Peptide-45 (BNP-45) in rats is a peptide that researchers extensively study to understand
cardiovascular functioning and disease mechanisms. Particularly, BNP-45 is a significant component in
physiological investigations because of its functional role as a hormone that helps regulate blood
pressure and fluid balance in the body. In a biological context, BNP-45 is of considerable interest
because it is secreted by the cardiac ventricles in response to excessive stretching of the heart muscle
cells (cardiomyocytes). This process is crucial since it signifies that the heart is working under
stress, often due to factors leading to cardiovascular diseases like heart failure and hypertension.
Research involving BNP-45 focuses significantly on its vasoactive properties. Studies reveal
that BNP-45 contributes to vasodilation, which helps lower blood pressure by widening blood vessels,
thus enhancing the understanding of its therapeutic potential in managing conditions like hypertension.
Furthermore, BNP-45’s natriuretic effects, wherein it promotes sodium excretion, help maintain fluid
balance and reduce blood volume—another crucial factor in managing heart disease and other related
conditions. Additionally, BNP-45 influences lipid metabolism and has lipolytic properties, which further
contribute to its cardiovascular protective roles.
Understanding BNP-45’s intricate involvement
in signaling pathways and cellular responses extends its importance to experimental therapies and
screening for cardiovascular disorders. Researchers study the expression levels of BNP-45 as biomarkers
to assess and predict heart failure and assess therapy outcomes. Thus, the role of BNP-45 in rats offers
a foundational basis to explore genetic, molecular, and therapeutic aspects that have translational
relevance to human cardiovascular research. The knowledge derived from these studies often leads to
biomarker development and novel cardiovascular therapies, making BNP-45 a vital research component
despite being studied primarily in the context of rodents.
How is Brain Natriuretic Peptide-45
(rat) used in laboratory settings, and what are the common experimental procedures?
In laboratory
settings, Brain Natriuretic Peptide-45 (BNP-45), derived from rats, is utilized predominantly in
experimental models aimed at cardiovascular research. Its primary usage involves studying the biological
effects of BNP on heart tissue and analyzing mechanisms underlying heart-related ailments such as
congestive heart failure and hypertension. Researchers employ various experimental procedures to assess
BNP-45’s influence on cardiac functioning.
One common experimental approach is using rat models
that simulate human cardiovascular conditions. These models help evaluate BNP-45’s physiological impact
and therapeutic potential. Researchers might induce heart stress in rodents by employing surgical
procedures or pharmaceuticals that mimic heart disease conditions. This setup allows them to measure the
in vivo effects of BNP-45 including its capacity to induce vasodilation, influence cardiac remodeling,
and promote natriuresis. Behavioral studies are also conducted to understand how BNP-45 modulates
cardiovascular responses under different physiological and pathophysiological conditions.
In
vitro studies are essential for dissecting molecular pathways mediated by BNP-45. Researchers often use
cultured cardiomyocytes or tissue extracts from rat hearts to examine BNP-45’s receptor interactions and
subsequent cellular responses. Techniques such as ELISA (enzyme-linked immunosorbent assay) and Western
blotting are employed to measure protein expression and secretion levels, thereby assessing BNP’s
regulatory functions. Patch-clamp recordings might be used to investigate ion channel activity in
cardiomyocytes, elucidating BNP-45’s role in cardiac electrophysiology.
Furthermore, molecular
studies on gene expression using qPCR (quantitative polymerase chain reaction) or RNA sequencing provide
insights into the signaling cascades activated by BNP-45. This involves exploring the gene networks and
molecular targets modulated by BNP-45, thereby expanding understanding of its impact on cardiac function
at the genetic level.
Researchers also employ imaging techniques such as MRI and echocardiography
in live rat models to visualize cardiac structure and function noninvasively. This enables the study of
BNP-45 in real-time physiological conditions and the investigation of its potential to reverse or
mediate cardiac hypertrophy and fibrosis. Overall, the application of BNP-45 in laboratory settings
allows for a comprehensive analysis of its biological functions, facilitating the development of new
therapeutic strategies for cardiovascular diseases.
What research advancements have been made
using Brain Natriuretic Peptide-45 (rat) in cardiovascular disease?
The utilization of Brain
Natriuretic Peptide-45 (BNP-45) in rat models has significantly advanced our understanding of
cardiovascular disease and its treatment. Over the years, BNP-45 has been integral in elucidating
mechanisms by which the body regulates blood pressure and fluid balance, leading to groundbreaking
findings in heart disease management. These advancements manifest across several key areas of research,
influenced heavily by the study of BNP-45.
One major advancement facilitated by BNP-45 studies is
in our comprehension of heart failure biomarkers. Research indicates that elevated BNP levels correlate
with heart failure severity, making BNP a crucial diagnostic and prognostic tool. The use of BNP-45 in
rat models has validated these findings, reinforcing the peptide’s status as a reliable marker for early
detection and monitoring of heart failure progression.
Additionally, BNP-45 research has
contributed significantly to the development of therapeutic strategies for cardiovascular disease. The
peptide’s ability to induce vasodilation and natriuresis as demonstrated in animal studies points to
potential antihypertensive therapies. Researchers have experimented with synthetic analogs and
modulators of BNP pathways, derived from BNP-45 insights, as candidate treatments. Some of these
strategies aim at enhancing BNP signaling to exert beneficial effects on cardiac load and blood pressure
regulation.
At the cellular and molecular level, BNP-45 studies have enhanced knowledge of
cardiac remodeling processes. Findings suggest BNP-45’s involvement in modulating cardiomyocyte
proliferation and apoptosis, which are pivotal in the pathogenesis of cardiac hypertrophy and heart
failure. Experimental rat models have shown that BNP-45 influences pathways related to oxidative stress
and inflammation, both critical contributors to cardiac remodeling. This insight offers a targeted
approach toward minimizing detrimental cardiac changes during disease progression.
Moreover,
BNP-45 research has fostered advancements in understanding lipid metabolism’s role in cardiovascular
health. Rat studies involving BNP-45 have demonstrated its lipolytic properties and potential impact on
adipose tissue regulation, thereby linking lipid metabolism closely with cardiac health outcomes.
Exploring these metabolic pathways offers promise for therapeutic interventions that address
cardiovascular risk factors such as obesity and metabolic syndrome.
Overall, research involving
BNP-45 in rats provides a compelling cross-section of progress in cardiovascular disease understanding
and management. These advancements underscore the translational aspects of BNP-45 research, where
findings from rat models pave the way for human applications, refining both diagnosis and therapy of
cardiovascular conditions.
What are the potential therapeutic applications of Brain Natriuretic
Peptide-45 derived from rat studies?
Brain Natriuretic Peptide-45 (BNP-45), although studied
primarily in rat models, holds substantial promise for therapeutic applications in human cardiovascular
diseases. The therapeutic potential of BNP-45 arises from its foundational role in regulating
cardiovascular homeostasis, primarily due to its effects on vasodilation, natriuresis, and cardiac
remodelling. Exploration of these effects in rodent models provides a translational platform for
extending these applications to humans.
One of the promising therapeutic directions is the
management of heart failure, a condition characterized by inadequate cardiac output and fluid retention.
BNP-45’s role in promoting vasodilation addresses the elevated blood pressure common in heart failure
patients. Synthetic forms of BNP or agonists that stimulate similar pathways are being explored to
reduce cardiac stress, improve organ perfusion, and ultimately, patient outcomes. Clinical parallels
have been drawn from rat studies demonstrating BNP-45’s efficacy in reducing cardiac load.
In
treating hypertension, the BNP pathway offers an innovative angle. Hypertension often coexists with
heart failure, raising the stakes of finding effective treatments. The natriuretic and vasodilatory
functions of BNP-45 observed in rodent studies indicate its potential as a supplementary treatment in
managing high blood pressure. Pharmacologically enhancing BNP signaling can aid in sodium excretion and
vascular relaxation, thus serving as a complement to existing antihypertensive
therapies.
Moreover, BNP-45’s involvement in lipid metabolism opens therapeutic avenues for
metabolic syndromes, including obesity-linked cardiovascular risks. Rat studies demonstrate BNP-45’s
influence on reducing lipid accumulation and enhancing lipolysis, suggesting a potential role in
managing dyslipidemia and ameliorating obesity-related cardiac dysfunctions. Targeting metabolic
pathways linked to BNP-45 could lead to comprehensive strategies addressing both cardiovascular and
metabolic health.
Additionally, BNP-45’s anti-inflammatory and anti-fibrotic properties, as
evidenced in rat studies, suggest its utility in managing myocardial fibrosis and inflammation
associated with cardiac diseases. These properties could be exploited to develop therapies that prevent
or reverse pathological cardiac remodelling, reducing progression to heart failure.
Finally,
advancements in gene therapy provide another futuristic application, leveraging BNP-45 pathways.
Modulating gene expression in BNP-related signaling may offer targeted interventions to enhance
endogenous BNP production or mimic its effects in patients with deficient BNP activity, thus
personalizing treatment approaches for specific patient populations.
In conclusion, rat model
studies of BNP-45 not only advance the biological understanding of this peptide but also offer a
blueprint for therapeutic strategies potentially transforming cardiovascular disease management. Each
proposed application reflects the intricate interplay of BNP’s physiological functions and its broader
impact on cardiovascular health.
How does research involving BNP-45 in rat models contribute to
biomarker development for human heart disease?
Research on Brain Natriuretic Peptide-45 (BNP-45)
in rat models plays an instrumental role in developing biomarkers for human heart disease by providing
foundational insights into the peptide’s physiological roles and its association with pathological
states. Biomarker discovery is an essential aspect of modern medicine, offering means for early
diagnosis, disease monitoring, and evaluation of therapeutic efficacy, especially in cardiovascular
diseases. BNP-45 research advances this field in several significant ways.
Firstly, rat studies
demonstrate how BNP-45 expression correlates with specific cardiac stress conditions such as volume
overload, hypertension, and heart failure. By elucidating the peptide’s interaction with these
stressors, researchers can establish its value as a predictive biomarker for similar conditions in
humans. The ability to measure circulating BNP levels offers a non-invasive diagnostic tool that can
indicate the presence and severity of heart stress or dysfunction, thus aiding in early detection and
intervention.
Secondly, BNP-45 research delineates the molecular pathways and gene networks
regulated by this peptide, shedding light on the signaling cascades critical for maintaining
cardiovascular health. This knowledge fosters the development of companion biomarkers based on the
expression of BNP-related genes or post-translational modifications of BNP, enhancing disease
specificity and diagnostic precision. As researchers understand more about BNP-45’s regulatory roles and
downstream effects, they can design assays and technologies to accurately quantify these parameters in
human subjects.
Furthermore, rat model research highlights BNP-45’s dynamic response to
therapeutic interventions, proving its utility in monitoring treatment outcomes. For instance, declining
BNP levels in response to effective cardiac treatment can function as a biomarker for therapeutic
success, helping clinicians refine treatment regimens and make informed decisions about patient care.
Similarly, persistent or elevating BNP levels might signal treatment failure or disease progression,
necessitating timely therapeutic adjustments.
In studies involving different strains or
genetically modified rats, variations in BNP expression assist in identifying genetic predispositions to
heart disease, thus contributing to personalized medicine approaches. Understanding individual
differences in BNP regulation can lead to biomarker development that accounts for genetic variability,
improving risk stratification and targeted interventions in diverse populations.
Lastly, BNP-45’s
investigation in rat models paves the way for exploring combination biomarkers that can encompass BNP
alongside other peptides or cytokines, offering a comprehensive profile of cardiovascular health. Such
multiplexed approaches can increase diagnosis accuracy and provide insights into the multifaceted nature
of cardiovascular diseases, where BNP serves as a central component of a broad diagnostic
toolkit.
Overall, BNP-45 research in rat models underpins biomarker innovation for human heart
disease by translating preclinical discoveries into clinical applications that improve patient outcomes
and precision in cardiovascular care.