Synonym |
NPY (3-36) (porcine) |
Species |
Porcine |
Protein Accession |
P01337 |
Purity |
≥ 95% |
Endotoxin Level |
< 1.0 EU per 1 μg of the protein |
Biological Activity |
Not specified |
Expression System |
E. coli |
Fusion Tag |
No tag |
Predicted Molecular Mass |
Approximately 3377 Da |
Formulation |
Lyophilized |
Reconstitution |
Reconstitute in H₂O to a concentration of 0.1-1.0 mg/ml |
Storage & Stability |
Store lyophilized protein at -20°C. Aliquot the product after reconstitution to avoid repeated
freezing/thawing cycles |
FAQ
What is Neuropeptide Y (3-36) (porcine) and how does it differ from other fragments or forms of
Neuropeptide Y?
Neuropeptide Y (NPY) is a highly conserved peptide that plays a significant role
in various physiological processes, including energy metabolism, appetite regulation, anxiety, and
cardiovascular functions. Among its many derivatives or fragments, Neuropeptide Y (3-36) (porcine) is a
notable form. This specific fragment is a truncated version of the full-length peptide, missing some
amino acids at the N-terminal end, which can influence its receptor affinity and functional properties
compared to the full-length Neuropeptide Y.
The primary distinction between Neuropeptide Y (3-36)
and other forms of NPY lies in its receptor selectivity. While full-length NPY can interact with several
receptor subtypes, including Y1, Y2, Y4, and Y5, the (3-36) fragment predominantly acts as an agonist
for the Y2 receptor subtype. This selective interaction impacts its functional role significantly; for
instance, the Y2 receptors are mostly prejunctional and often mediate an inhibitory feedback mechanism.
This means that NPY (3-36) primarily influences processes involving inhibition rather than stimulation,
offering unique insights into its biological impact.
From a physiological perspective, the
preferential action of NPY (3-36) on Y2 receptors has been linked with the regulation of food intake.
Research indicates that this fragment can inhibit food consumption by modulating the signaling pathways
involved in appetite suppression. This differs from the full-length NPY, which often stimulates food
intake through other receptor pathways. Consequently, Neuropeptide Y (3-36) has drawn attention for its
potential implications in obesity research and understanding satiety mechanisms.
Another factor
to consider is the source, with the porcine version of this peptide being used frequently in both
research and practical applications. The porcine model offers insights into mammalian biology that are
often relevant to human physiology, given the similarities between pig and human biology. This makes the
study of Neuropeptide Y (3-36) (porcine) particularly valuable for translational research that may
eventually impact therapeutic approaches in humans.
On a molecular level, the differentiation
between the NPY forms also extends to their biostability and degradation rates. Truncated forms like NPY
(3-36) could exhibit different metabolic half-lives compared to their full-length counterparts.
Understanding the specific degradation pathways and stability in various environments can be crucial
when utilizing these peptides in therapeutic or research contexts.
In summary, Neuropeptide Y
(3-36) (porcine) distinguishes itself mainly through receptor specificity, physiological role, and its
valuable application as a model in porcine biology. These characteristics make it a subject of interest
in scientific studies focusing on appetite regulation, energy balance, and potential therapeutic avenues
for metabolic disorders.
How is Neuropeptide Y (3-36) (porcine) relevant to current research in
appetite and energy balance?
Neuropeptide Y (3-36) (porcine) is extensively studied for its
significant role in the regulation of appetite and energy balance, making it a crucial subject in
current biomedical research. This specific fragment of Neuropeptide Y, due to its preferential binding
to Y2 receptors, allows researchers to delve into the complex mechanisms governing food intake and
energy homeostasis with a focus on inhibition pathways.
The relevance of NPY (3-36) in appetite
research is anchored in its ability to influence neuroendocrine pathways that control hunger and
satiety. Studies have revealed that NPY (3-36) acts as a satiety signal, modulating the central nervous
system's response to hunger signals. The Y2 receptor, primarily expressed in the hypothalamus—an area of
the brain critical for energy regulation—mediates these effects. When activated, the Y2 receptor can
potentially reduce the release of orexigenic signals, which promote feeding, thus providing a mechanism
for appetite suppression. This has sparked interest in its therapeutic potential for obesity and related
metabolic disorders, as controlling excessive food intake is a primary goal in managing such
conditions.
Furthermore, Neuropeptide Y (3-36) is investigated for its role in energy expenditure
and storage. It is part of a broader set of pathways that determine how effectively the body burns
calories and stores fat. By influencing the autonomic nervous system's balance between sympathetic and
parasympathetic activity, NPY (3-36) can affect how energy is distributed and utilized, playing a
possible role in conditions like metabolic syndrome, which includes symptoms like insulin resistance and
hyperlipidemia.
Research has also explored the potential of NPY (3-36) in stress-related eating
behaviors. Since stress is known to increase the expression of Y1 receptors which promote feeding, the
action of NPY (3-36) on Y2 receptors could offer a counterbalance by promoting feelings of fullness and
reducing stress-induced eating.
Furthermore, NPY (3-36) might provide a tool for distinguishing
between the neural pathways and hormonal signals that separately govern different types of hunger and
energy use, whether prompted by caloric deficiency, ghrelin-induced hunger, or habitual eating patterns.
By employing models that utilize Neuropeptide Y (3-36), researchers can build a more comprehensive
picture of these diverse and often overlapping systems.
Additionally, the relevance of the
porcine model in this research cannot be overstated. Pigs and humans share similar physiological
processes related to digestion and metabolic regulation. Using Neuropeptide Y (3-36) (porcine) helps
bridge the gap between basic animal research and human clinical applications. It allows for the
development of potential therapeutic interventions to modify appetite and energy balance
effectively.
Thus, Neuropeptide Y (3-36) (porcine) continues to be a valuable research focus due
to its potential to yield new insights into the treatment of obesity, metabolic disorders, and related
conditions. Its unique receptor interactions and physiological roles make it a key player in the ongoing
quest to understand appetite and energy regulation at a molecular level.
What are the potential
therapeutic implications of Neuropeptide Y (3-36) (porcine) in treating metabolic
disorders?
Neuropeptide Y (3-36) (porcine) has garnered significant attention in the field of
therapeutic research, particularly for its promising implications in the management and treatment of
metabolic disorders. Metabolic disorders, encompassing conditions such as obesity, type 2 diabetes, and
metabolic syndrome, are characterized by disruptions in energy balance, glucose metabolism, and lipid
profiles. The selective action of Neuropeptide Y (3-36) on Y2 receptors positions it as a potential
target in the therapeutic landscape for these conditions.
One of the primary therapeutic
implications of NPY (3-36) lies in its ability to regulate appetite and energy intake. By acting as an
agonist for the Y2 receptor, it contributes to the reduction of food intake. This attribute is
particularly relevant in the treatment of obesity, a condition fundamentally driven by an imbalance
between caloric intake and expenditure. By modulating the signaling pathways that enhance satiety, NPY
(3-36) could help reduce excessive food consumption, thus facilitating weight loss and improvements in
health markers associated with obesity, such as insulin sensitivity and lipid profiles.
Moreover,
NPY (3-36)'s influence on energy homeostasis extends to the modulation of energy expenditure. This could
aid in shifting the energy balance toward increased calorie burning as opposed to storage, which is a
beneficial factor in the management of obesity and related disorders. This shift in energy dynamics is
critical as it can contribute to both immediate metabolic improvements and long-term weight management,
reducing the risk of comorbidities like cardiovascular disease and type 2 diabetes.
In the
context of type 2 diabetes, Neuropeptide Y (3-36) may play a role in modulating glucose metabolism and
improving insulin sensitivity. By reducing food intake and potentially altering adiposity, NPY (3-36)
might help mitigate hyperglycemia and improve pancreatic function. This is significant because type 2
diabetes is often accompanied by insulin resistance—a state where the body's cells fail to respond
appropriately to insulin, leading to elevated blood sugar levels. Therapeutic strategies that involve
appetite regulation and weight management, facilitated by peptides like NPY (3-36), are integral to
addressing insulin resistance and enhancing glycemic control.
Furthermore, preliminary research
suggests that the anxiety-reducing effects of Y2 receptor activation might also help mitigate the
stress-induced exacerbation of metabolic symptoms. Stress is a known contributor to metabolic
dysfunction, promoting poor eating habits and increased abdominal fat deposition through hormonal
pathways involving cortisol and NPY. By providing mechanisms that can curb stress-related eating and
improve emotional well-being, NPY (3-36) holds potential in comprehensive metabolic disorder
interventions.
It is critical to acknowledge that translating these potential therapeutic
implications into clinical applications requires extensive research and clinical trials. Safety
profiles, efficacies, optimal dosages, and delivery mechanisms are key areas that need thorough
investigation. Nevertheless, the promising action of Neuropeptide Y (3-36) (porcine) offers a foundation
for developing novel therapies that address both the physiological and behavioral components of
metabolic disorders.
Overall, by targeting key pathways involved in appetite regulation and
energy metabolism, Neuropeptide Y (3-36) (porcine) may be a pivotal component in future multi-faceted
treatment strategies for metabolic disorders. This highlights its importance not only in advancing
scientific understanding but also in potentially guiding effective therapeutic interventions.
How
does Neuropeptide Y (3-36) (porcine) influence cardiovascular health and are there potential
applications in treating cardiovascular diseases?
Neuropeptide Y (3-36) (porcine) offers
intriguing potential regarding its influence on cardiovascular health and its application in managing
cardiovascular diseases. The cardiovascular system is intricately regulated by neuroendocrine signaling,
where peptides like NPY play critical roles in controlling blood pressure, heart rate, and vascular
tone. NPY (3-36) distinguishes itself by interacting primarily with the Y2 receptors, offering unique
insights and therapeutic possibilities.
One of the notable cardiovascular effects of Neuropeptide
Y (3-36) is its capacity to modulate blood vessel constriction. Research indicates that NPY (3-36),
through Y2 receptor interaction, might have vasodilatory effects under specific circumstances. This
contrasts with full-length NPY, which is generally associated with vasoconstriction. By influencing
vascular tone, NPY (3-36) could contribute to blood pressure regulation. This regulatory capacity makes
it a subject of interest in conditions characterized by dysregulated vascular tone, such as
hypertension—a major risk factor for various cardiovascular diseases.
Cardiovascular health also
benefits from the potential of NPY (3-36) to influence sympathetic nervous system activity. The peptide
may help modulate sympathetic outflow, a factor crucial in cardiovascular disease contexts. Dysregulated
sympathetic activity is implicated in heart failure and arrhythmias, where excessive sympathetic
stimulation can exacerbate these conditions. By potentially reducing sympatho-excitatory actions via Y2
receptor activation, NPY (3-36) could offer therapeutic benefits in managing such
disorders.
Moreover, the anti-inflammatory and stress-related aspects of cardiovascular health
connect with NPY (3-36)'s potential therapeutic uses. Cardiovascular diseases are often accompanied by
inflammatory processes and psychological stress, which can exacerbate disease progression. The role of
NPY (3-36) in stress reduction through central nervous system effects might offer an auxiliary benefit
in comprehensive cardiovascular risk management.
It is essential to highlight that the
therapeutic application of NPY (3-36) in cardiovascular diseases is still in exploratory phases, with
much of the current understanding derived from preclinical models. Translational research is essential
to ascertain its efficacy and safety in human subjects. Investigations into how NPY (3-36) could be
integrated with current cardiovascular therapies—whether as an adjunct treatment that enhances existing
therapies or as a standalone intervention—are crucial for future applications.
The porcine
model’s biological similarity to humans in cardiovascular physiology presents an excellent opportunity
for research. By analyzing how NPY (3-36) operates within this model, researchers can gain insights that
may eventually guide clinical applications. Potential clinical applications may range from therapeutic
agents that mitigate specific cardiovascular risk factors, or novel treatments designed to address
multifaceted aspects of cardiovascular health such as inflammation, dysregulated sympathetic activity,
and stress-related cardiovascular damage.
In summary, Neuropeptide Y (3-36) (porcine) holds
promise for influencing cardiovascular health through its effects on vascular tone, sympathetic nervous
system modulation, and potentially reducing stress and inflammation associated with cardiovascular
diseases. However, further studies and clinical research are needed to fully unlock and validate its
potential therapeutic applications in cardiovascular care.
Can Neuropeptide Y (3-36) (porcine)
play a role in neuropsychiatric conditions, and what are the mechanisms involved?
Neuropeptide Y
(3-36) (porcine) is emerging as a subject of interest in the study of neuropsychiatric conditions,
thanks to its potential influence on neurological and behavioral processes. Its interaction primarily
with Y2 receptors offers unique insights into its role in brain function, emotional regulation, and
stress response, making it relevant in contexts such as anxiety, depression, and stress-related
disorders.
Neuropeptide Y (3-36) has shown potential in modulating anxiety and depression through
its action on Y2 receptors, which are prevalent in brain regions involved in emotion and stress, such as
the hippocampus, amygdala, and prefrontal cortex. The Y2 receptor, when activated, is often associated
with anxiolytic and antidepressant effects. This aligns with research suggesting that NPY (3-36) might
play a protective role against stress-induced anxiety and mood dysregulation. The peptide's ability to
promote inhibitory signaling in stress-related pathways could lead to reduced anxiety and improved mood
stability, positioning it as a potentially interesting candidate for therapeutic development in managing
anxiety and depressive disorders.
Another neuropsychiatric area where Neuropeptide Y (3-36)
(porcine) may exert influence is stress resilience and adaptation. Stress is a prevalent factor
contributing to numerous mental health issues, and the ability to adaptively respond to stressors is
crucial for psychological well-being. NPY (3-36) may enhance stress resilience by modulating the brain's
response to stress at a molecular level, possibly impacting the hypothalamic-pituitary-adrenal (HPA)
axis. This modulation could lead to reduced cortisol release and a balanced stress response, which is
beneficial for maintaining mental health under acute or chronic stress conditions.
Moreover, the
role of Neuropeptide Y (3-36) in regulating food intake and body weight might also contribute to its
effects on neuropsychiatric conditions. Eating disorders, for example, have psychological components
linked to stress, anxiety, and depression. By influencing appetite and stress pathways concurrently, NPY
(3-36) could offer a dual approach in managing the neuropsychiatric dimensions of these
conditions.
Furthermore, the porcine model is conducive to translating preclinical
neuropsychiatric research to human contexts due to its similarities in brain structure and function.
This makes studies involving Neuropeptide Y (3-36) (porcine) particularly valuable in hypothesizing
human applications.
However, it is crucial to conduct further studies, including clinical trials,
to better understand and validate the neuropsychiatric implications of NPY (3-36). Identifying the
precise pathways and dosages required for therapeutic effect, as well as potential side effects, remains
an essential part of this research domain. These efforts could ultimately lead to novel interventions
for mental health conditions, harnessing the unique receptor actions and biological effects of
Neuropeptide Y (3-36) (porcine).
In summary, Neuropeptide Y (3-36) (porcine) holds promising
potential in neuropsychiatric research due to its capacity to modulate mood, stress resilience, and
emotional regulation through Y2 receptor interactions. Its dual ability to influence neuroendocrine and
behavioral pathways could be advantageous in developing comprehensive treatment strategies for various
neuropsychiatric conditions. Nonetheless, continued research is crucial to fully elucidate its
therapeutic potential and establish its application in clinical settings.