Taiy Chemical
Brain Natriuretic Peptide-45 (rat)
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.
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