Synonym |
Neuropeptide Y (free acid) |
Species |
Human, rat |
Protein Accession |
P01303 |
Purity |
> 95% |
Endotoxin Level |
< 1.0 EU per 1 μg of protein |
Biological Activity |
Not specified |
Expression System |
Not specified |
Fusion Tag |
None |
Predicted Molecular Mass |
Approximately 4.7 kDa |
Formulation |
Lyophilized from a 0.2 μm filtered solution of acetic acid |
Reconstitution |
Reconstitute in water to a concentration of 0.1-1.0 mg/ml |
Storage & Stability |
Store at -20°C upon receipt. Stable for up to 12 months at -20°C |
FAQ
What is Neuropeptide Y (free acid) (human, rat), and what roles does it play in the
body?
Neuropeptide Y (NPY) is one of the most abundant peptides in the mammalian brain and is
found in both humans and rats. It is a 36-amino acid peptide that belongs to the pancreatic polypeptide
family and is widely distributed in the central nervous system and various peripheral tissues. In the
body, NPY plays a multitude of roles across a range of physiological processes. In the central nervous
system, it is predominantly expressed in the brain regions associated with the hypothalamus,
particularly the arcuate nucleus, paraventricular nucleus, and the ventromedial hypothalamus, which are
key areas implicated in energy homeostasis and the regulation of appetite. One of the primary roles of
NPY is its ability to induce appetite and food intake. It is considered one of the most potent
orexigenic (appetite-stimulating) peptides known. The secretion of NPY is upregulated during energy
deficit states, such as fasting or food deprivation, resulting in an increase in feeding behavior.
Moreover, NPY is also involved in energy storage and adipose tissue function, promoting lipogenesis and
decreasing energy expenditure. Beyond its influence on energy balance and appetite, NPY also plays an
important role in stress response, circadian rhythm regulation, cardiovascular function, and
neuroprotection. During times of stress, NPY is secreted and acts to dampen the effects of stress by
reducing anxiety-like behaviors, indicating its anxiolytic properties. It also modulates circadian
rhythms and sleep by interacting with various neurotransmitter systems in the brain. NPY's role in
cardiovascular function involves the modulation of blood pressure and heart rate. It acts as a potent
vasoconstrictor and can influence peripheral resistance, contributing to the regulation of blood
pressure. Additionally, NPY exhibits neuroprotective effects, helping to protect neurons from damage
during instances of ischemic injury or other neurotoxic insults.
Why is Neuropeptide Y (free
acid) (human, rat) an important molecule for scientific research?
Neuropeptide Y (NPY) is an
important molecule for scientific research due to its diverse roles in physiological and pathological
processes, making it a critical target for understanding and potentially treating a variety of
conditions. One of the main reasons for studying NPY is its significant involvement in regulating energy
balance and metabolism. Researchers are particularly interested in its role in the pathogenesis of
obesity and related metabolic disorders. Since NPY is known for its ability to stimulate appetite and
promote energy storage, understanding its mechanisms of action could lead to novel therapeutic
approaches for obesity and conditions like type 2 diabetes, where energy balance is disrupted.
Furthermore, NPY's involvement in stress response and anxiety implies that it could be a valuable target
for research on psychiatric disorders. By elucidating how NPY modulates stress and anxiety, scientists
hope to develop new interventions for anxiety disorders, depression, and potentially other
stress-related conditions. Insights from these studies could lead to more effective treatments with
fewer side effects compared to current options. In addition to its roles in metabolism and stress
response, NPY's function in cardiovascular physiology makes it relevant to research focused on
hypertension, heart failure, and other cardiovascular diseases. Exploring how NPY affects
vasoconstriction and cardiac function can offer potential therapeutic pathways for managing these
conditions. The peptide's neuroprotective properties also make it an intriguing subject for research in
neurodegenerative diseases. Studies investigating NPY's neuroprotective mechanisms could lay the
groundwork for new strategies to mitigate neuronal damage in disorders such as Alzheimer's disease,
Parkinson's disease, and stroke. Lastly, as a peptide with high conservation across species, NPY
provides a valuable model for comparative studies in humans and other mammals, such as rats, which are
commonly used in experimental research. This cross-species similarity enables translational research
where findings from animal models can be more readily applied to human physiology and medicine.
How does Neuropeptide Y (free acid) (human, rat) impact appetite regulation, and what
implications does this have for understanding obesity?
Neuropeptide Y (NPY) plays a central role
in the regulation of appetite and is one of the most potent stimulators of feeding behavior in both
humans and rats. Its impact on appetite regulation is primarily exerted through its actions within the
hypothalamus, particularly the arcuate nucleus. NPY is co-expressed with another neuropeptide called
agouti-related peptide (AgRP), and both act synergistically to increase hunger and stimulate food
intake. NPY is released in response to an energy deficit in the body, such as during fasting or calorie
restriction, and it acts by promoting feeding and reducing energy expenditure to restore energy balance.
It achieves this effect by interacting with Y1 and Y5 receptors in the brain, which are known to mediate
its orexigenic actions. The significance of NPY in appetite regulation and its implications for obesity
revolve around its ability to modulate various neurobiological pathways that control hunger and satiety.
In individuals with dysregulated NPY signaling, there can be an exaggerated drive to eat, contributing
to excessive calorie intake and the development of obesity. In conditions where there is chronic energy
surplus, such as obesity, the regulatory mechanisms that control NPY expression can become disrupted,
possibly leading to a persistent state of increased hunger. Understanding the mechanisms by which NPY
influences appetite provides invaluable insights into the development and perpetuation of obesity. It
opens avenues for potential therapeutic interventions targeting the NPY system to help manage excessive
food consumption. For instance, the development of antagonists or inhibitors that block NPY receptors
could help reduce appetite and aid in weight management. Additionally, modifying lifestyle factors that
influence NPY expression, such as nutrition and stress management, may also have beneficial implications
for controlling obesity. Moreover, research on NPY can contribute to personalized treatment approaches
for obesity, wherein interventions are tailored based on an individual's specific neuropeptide
expression and regulation patterns. By advancing our understanding of how NPY functions and interacts
with other appetite-regulating mechanisms, researchers can identify precise targets for combating
obesity and related metabolic disorders.
What are the effects of Neuropeptide Y (free acid)
(human, rat) on stress and anxiety, and how might this knowledge be applied in clinical
settings?
Neuropeptide Y (NPY) is known for its significant modulatory effects on stress and
anxiety, functioning as a vital part of the body's response to stressors. NPY is widely distributed in
the brain, with high concentrations found in regions associated with stress and emotion regulation, such
as the amygdala, hippocampus, and periaqueductal gray. During stressful conditions, NPY is released as a
coping mechanism to mitigate the effects of stress and anxiety, acting as an anxiolytic agent by
interacting with its receptors in the brain. NPY reduces the release of corticotropin-releasing factor
(CRF), a key hormone that drives the hypothalamic-pituitary-adrenal (HPA) axis response to stress. By
dampening the stress response, NPY contributes to a decrease in anxiety-like behaviors and promotes
resilience to stress. Furthermore, NPY has been shown to enhance neurogenesis and neuronal survival in
the hippocampus, a region critical for regulating mood and emotion. The augmentation of neurogenesis by
NPY can counteract the negative effects of chronic stress, such as anxiety and depression. The potential
application of knowledge regarding NPY's role in stress and anxiety is vast, particularly in clinical
settings. Understanding how NPY functions as a natural anxiolytic opens possibilities for harnessing its
effects to develop treatments for anxiety-related disorders and depression. One application could be the
development of pharmaceutical agents that enhance NPY activity or mimic its effects, potentially
providing new interventions with anxiolytic properties. Additionally, personalized medicine approaches
could emerge where patients with heightened stress sensitivity or anxiety disorders are evaluated for
NPY levels or receptor function, allowing for tailored therapeutic strategies targeting the NPY system.
Identifying individuals with specific genetic or expression profiles related to NPY could lead to more
effective management of stress-related conditions. Beyond pharmacological treatments, this knowledge
could improve cognitive-behavioral therapies by incorporating strategies that align with enhancing
natural NPY production or activity through lifestyle changes, such as exercise and stress management
techniques. Physical activity, for instance, has been shown to increase NPY levels, suggesting that
exercise programs could be designed to harness this effect to alleviate anxiety symptoms. Overall, the
insights into NPY's influence on stress and anxiety not only expand the understanding of these complex
conditions but also pave the way for innovative therapeutic approaches that enhance quality of life for
individuals affected by stress and anxiety disorders.
What research methodologies are commonly
used to study Neuropeptide Y (free acid) (human, rat), and how have these studies advanced our
understanding of its functions?
Research methodologies used to study Neuropeptide Y (NPY)
encompass a diverse array of techniques, enabling comprehensive exploration of its biological roles and
mechanisms. One common methodology involves the use of animal models, predominantly rodents, due to the
high degree of homology between rat and human NPY systems. In vivo studies with genetically modified
mice, such as knockout or transgenic models, allow researchers to observe the physiological and
behavioral consequences of altered NPY expression or receptor function. These models have been pivotal
in elucidating the roles of NPY in appetite regulation, stress response, and energy homeostasis.
Molecular biology techniques, such as in situ hybridization and quantitative PCR, are employed to assess
NPY mRNA expression and localization in various tissues, providing insights into the regulation of its
gene expression. Immunohistochemistry and Western blotting techniques are also utilized to detect and
quantify NPY peptides and their receptors at the protein level, thereby advancing understanding of their
distribution and functional status across different physiological states. Electrophysiological
approaches are used to study the effect of NPY on neuronal activity, particularly in brain regions
associated with its action. Patch-clamp recording and other electrophysiological methods reveal how NPY
modulates synaptic transmission and neuronal excitability, contributing to its influence on feeding
behavior and emotional regulation. Pharmacological studies using selective agonists or antagonists for
NPY receptors help delineate the specific receptor subtypes involved in mediating its effects. These
studies have been crucial in identifying the Y1, Y2, and Y5 receptors as significant players in NPY’s
appetite-stimulating and anxiolytic actions. Advanced imaging techniques, such as PET and MRI, are
employed to study NPY systems in vivo, providing a non-invasive means to monitor changes in receptor
activity and ligand interaction in real-time. These methodologies facilitate the observation of NPY's
role in human health and disease, translating findings from animal studies to clinical contexts.
Collectively, these diverse research methodologies have significantly advanced the scientific
understanding of NPY by elucidating its multifaceted roles in physiology and pathophysiology. Such
advancements have laid the groundwork for potential therapeutic interventions targeting NPY-related
pathways to treat conditions like obesity, anxiety disorders, and metabolic and cardiovascular diseases,
demonstrating the far-reaching impact of methodological innovation in NPY research.
What
potential therapeutic applications might arise from understanding the structure and function of
Neuropeptide Y (free acid) (human, rat)?
Understanding the structure and function of Neuropeptide
Y (NPY) holds significant promise for the development of novel therapeutic applications. Given its
extensive involvement in a range of physiological processes, NPY-related therapies could address various
medical conditions. One potential therapeutic application lies in the treatment of obesity and metabolic
disorders. As NPY is a potent stimulator of food intake and energy storage, modulating its activity
could help manage overeating and promote weight loss. Therapeutics that inhibit NPY’s action or block
its receptors, particularly the Y1 and Y5 receptors associated with appetite stimulation, could reduce
food intake and help control obesity. Such interventions could be pivotal in addressing the obesity
epidemic and related conditions like type 2 diabetes, where precise control of energy balance is
crucial. Another promising application is in the treatment of stress-related disorders and anxiety.
NPY’s anxiolytic properties highlight its potential as a target for developing new anxiolytic drugs that
could be more effective and have fewer side effects than current treatments. Enhancing NPY activity or
mimicking its effects through pharmacological agents could offer relief for individuals suffering from
anxiety disorders or depression, improving mental health outcomes. Additionally, NPY’s involvement in
neuroprotection opens avenues for therapeutic development in neurodegenerative diseases. Agents that
enhance NPY's neuroprotective effects could potentially slow the progression of diseases like
Alzheimer's and Parkinson's, providing a new strategy for preserving cognitive and motor functions in
affected individuals. In cardiovascular medicine, understanding NPY’s role could lead to treatments for
hypertension and heart failure. Since NPY influences vasoconstriction and blood pressure regulation,
therapies targeting its pathways might help manage high blood pressure or prevent cardiac incidents.
Personalized medicine could also benefit from insights into NPY function. Genetic testing and biomarker
analysis related to NPY could identify individuals who might especially benefit from targeted therapies,
allowing for tailored treatment regimens. The comprehensive understanding of NPY’s structure and
function also supports the development of lifestyle interventions that naturally regulate NPY levels.
For example, dietary modifications, exercise programs, and stress management techniques could be
optimized to influence NPY activity, complementing pharmacological strategies. Overall, the intricate
understanding of NPY offers vast potential for innovative therapeutic applications across multiple
domains of health, from metabolic conditions to mental health and cardiovascular treatments, marking a
significant step forward in personalized and disease-specific interventions.