Synonym |
None |
Species |
Rat |
Protein Accession |
P01161 |
Purity |
Greater than 95% as determined by SDS-PAGE |
Endotoxin Level |
Less than 1 EU per μg of the protein by the LAL method |
Biological Activity |
Not available |
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
Approximately 2400 Da |
Formulation |
Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA |
Reconstitution |
Reconstitute in water to a concentration of 0.1-1.0 mg/ml |
Storage & Stability |
Store at -20°C. For long term storage, store at -80°C. Stable for 3 months after receipt. |
FAQ
What is Neuropeptide W-23 and what is its significance in scientific research?
Neuropeptide W-23
(NPW-23) is a naturally occurring peptide discovered in the brain, with notable expression in tissues of
rat models. It forms part of a larger family of neuropeptides, which are small protein-like molecules
that neurons use to communicate with each other. NPW-23, specifically, has garnered significant
attention for its involvement in various physiological processes and its potential applications in
research spanning areas such as endocrinology, neurology, and behavior. NPW-23 has been linked to
functions including the regulation of feeding behavior, energy homeostasis, stress responses, and the
modulation of pain pathways. Its study could provide insights into complex biological pathways, making
it a valuable subject for scientists exploring fundamental brain activities and disorders. In research
circles, its relevance extends to examining obesity, metabolic disorders, mental health issues, and
understanding how the brain manages stress and pain. It is used particularly in preclinical studies
using rat models to evaluate its role and impact, providing a bridge to possible human applications.
Understanding NPW-23 fully requires robust research into its signaling mechanisms, receptor
interactions, and wider physiological roles, which underscores its value in advancing neuroscience and
related fields.
How is Neuropeptide W-23 administrated in a research setting, and what
considerations are necessary regarding its use?
When administering Neuropeptide W-23 in a research
setting, particularly in studies involving rat models, it's typically done using controlled dosing
methods that allow for precision and replicability. Common methods include intracerebroventricular (ICV)
injections, which deliver the peptide directly into the brain's ventricular system, ensuring direct
access to its targeted sites of action. This method is favored in studies focusing on neural mechanisms.
Alternatively, peripheral administration, such as subcutaneous or intraperitoneal injections, may be
used depending on the study design and objectives. Researchers considering the administration of NPW-23
need to be meticulous about several factors, including dosing concentrations, the timing of
administration, and the choice of delivery method, all of which are crucial for the study outcomes.
Rigorous controls and replication are essential to validate the findings reliably. The purity of NPW-23
used is critical, requiring comprehensive validation procedures to ensure no confounding results due to
impurities or miscalculations. It's also important to adhere strictly to ethical considerations,
consistent with Institutional Animal Care and Use Committees (IACUC) guidelines or their equivalents,
ensuring minimal discomfort and stress for animal subjects. Detailed monitoring post-administration is
vital to evaluate the effects and preemptively address possible adverse reactions. Researchers must
maintain high standards of record-keeping and experimental documentation to support the reproducibility
and integrity of the data collected, facilitating peer-review and publication processes.
What are
the primary physiological effects observed with the administration of Neuropeptide W-23 in rat models?
Research into Neuropeptide W-23 has unveiled several primary physiological effects once it is
administered in rat models, thus providing insights into its potential mechanisms of action. One of the
prominent effects observed is in appetite regulation and energy balance, where NPW-23 is noted to
influence feeding behaviors. Studies have shown that the administration of NPW-23 can result in
decreased food intake, implicating its role in satiety and weight management. It is postulated that
NPW-23 interacts with the hypothalamus, a critical brain area in energy homeostasis, to elicit these
changes. Additionally, NPW-23 is implicated in the modulation of stress responses. It is believed that
this peptide interacts with stress-activated pathways, potentially impacting corticosterone levels,
which are biomarkers for stress in animals. This effect highlights the role of NPW-23 in neuroendocrine
regulation. Also noteworthy are findings indicating that NPW-23 administration can modify pain
perception. Researchers have described shifts in pain threshold and an altered response to noxious
stimuli, suggesting its potential role in analgesia or pain management. The impact of NPW-23 on
neurotransmitter systems, particularly those related to dopamine and serotonin, has also been studied,
indicating broader implications in mood and behavioral disorders. There is a growing interest in the
potential that NPW-23 might interact with, or modulate, receptor pathways that are involved in
behavioral drives, neuroprotection, and cognitive functions. However, while many findings are promising,
much of the research remains at a preclinical stage. Further studies are needed to fully articulate the
pathways involved and the potential for therapeutic applications in complex physiological and
neurological conditions.
What is known about the receptor interactions of Neuropeptide W-23, and
what implications do these interactions have for research?
Neuropeptide W-23 interacts with specific
receptors primarily identified as G protein-coupled receptors (GPCRs), notably the NPBWR1 and NPBWR2
receptors, which are extensively studied for their role in neuromodulation and physiological regulation.
These receptors are widely expressed in the central nervous system, especially in regions associated
with emotion, stress, and reward systems, such as the hypothalamus, amygdala, and midbrain. The
interaction between NPW-23 and these receptors plays a vital role in its biological activities.
Understanding NPW-23's receptor interactions is essential for unraveling its functional pathways and
assessing its full potential in therapeutic contexts. These interactions contribute significantly to the
regulation of feeding behavior, stress response, and the pain management processes. For example, the
activation of NPBWR1 by NPW-23 has been shown to suppress food intake in rat models, suggesting
therapeutic implications for obesity and related metabolic disorders. Similarly, NPW-23’s influence on
stress-related pathways via receptor interactions offers potential insight into new treatment avenues
for anxiety and depression. Further research is needed to decipher the exact intracellular signaling
cascades triggered by these receptor interactions and their broader physiological impacts. The potential
for cross-talk between NPW-23 engaged pathways and other neuromodulatory systems also represents a
fertile area for future research, promising to deepen our understanding of neuropeptide function and its
connections with behavioral outcomes. The specificity and affinity of NPW-23 for its receptors, as well
as the pharmacodynamics involved, remain critical points of study, not only to elucidate how NPW-23
functions but also to potentially manipulate these interactions for therapeutic benefit.
What
potential does Neuropeptide W-23 have for therapeutic applications, based on current research findings?
Current research suggests that Neuropeptide W-23 holds considerable potential for therapeutic
applications, especially in conditions related to its primary physiological effects. The modulation of
feeding behaviors by NPW-23 points towards its use in addressing obesity and eating disorders. As
obesity and related metabolic syndrome represent a significant health burden globally, understanding and
leveraging NPW-23's mechanisms in appetite regulation could pave the way for developing novel weight
management therapies. Moreover, its role in stress modulation suggests applications in managing anxiety
disorders and depression. By targeting stress and mood regulation pathways, NPW-23 could provide
alternative strategies to conventional treatments, potentially offering fewer side effects and a
different mechanism of action. Importantly, NPW-23's observed effects on pain perception introduce
possibilities in analgesic development. Pain management remains a critical area of medical need, and
neuropeptides like NPW-23 could contribute to the formulation of new, more effective, and safer pain
relief medications, particularly in chronic and neuropathic pain conditions. The neuroprotective
attributes ascribed to NPW-23 also suggest possible applications in neurological disorders where
neuroprotection and synaptic plasticity are of therapeutic interest, such as in Alzheimer's or
Parkinson's disease. Despite these promising directions, it's important to note that much of the
research remains in preclinical stages, primarily in animal models. The translation from animal studies
to human treatments requires extensive further research, encompassing detailed investigations into
pharmacokinetics, safety profiles, and functional outcomes in human systems. Any therapeutic application
of NPW-23 will necessitate rigorous clinical trials to ensure efficacy and safety, reflecting the
complexity of neuropeptide functions and their interactions within the human body’s multisystem network.
This research direction emphasizes the importance of continued exploration into NPW-23, with the hope
that it will emerge as a cornerstone in designing the next generation of neuropharmacological
interventions.