Taiy Chemical
CART (61-102) (human, Rat)
Synonym CART (61-102)
Species Human, Rat
Protein Accession P63091
Purity > 95%
Endotoxin Level < 1.0 EU per 1 μg of protein
Biological Activity Not determined
Expression System E. coli
Fusion Tag None
Predicted Molecular Mass 4.7 kDa
Formulation Lyophilized from a 0.2 μm filtered solution in PBS
Reconstitution Centrifuge vial before opening. Reconstitute in sterile PBS, pH 7.4 to a concentration of 0.1-1.0 mg/ml.
Storage & Stability Store lyophilized protein at -20°C. Aliquot reconstituted protein and store at -20°C to -80°C. Avoid repeated freeze/thaw cycles.
FAQ
What is CART (61-102) and why is it significant in research involving humans and rats?

Cocaine- and amphetamine-regulated transcript (CART) peptides, particularly the CART (61-102) fragment, are receiving considerable attention in research due to their multifaceted roles in various physiological processes. Originally identified in 1981, CART peptides are neurotransmitters widely expressed in the central nervous system and peripheral tissues. Research indicates that CART (61-102) plays a critical role in regulating food intake and body weight, making it a vital focus in studies concerning obesity and metabolic disorders. The peptide is believed to act as an anorectic agent, meaning it suppresses appetite and food consumption. This property positions CART (61-102) as a key target for developing therapies for obesity and related metabolic diseases.

In the context of addiction research, CART peptides have been found to interact with the reward pathways in the brain, which are also implicated in the addictive processes of drugs like cocaine and amphetamines. Studies suggest that CART (61-102) might modulate the brain's response to these substances, offering potential pathways for therapeutic intervention in addiction cases. The peptide’s presence in mesolimbic pathways is significant because these areas are involved in emotional regulation and motivation, adding another layer of complexity to the behavioral implications of CART signaling.

In rat models, the administration of CART (61-102) has been shown to alter various behaviors associated with stress and anxiety. This suggests potential roles in stress response modulation, thus widening the scope of research from purely metabolic to psychiatric and behavioral domains. Research into human analogs is catching up, aiming to unpack similar modulating roles in human physiology and behavior. Moreover, understanding how CART (61-102) peptides work could lead to groundbreaking developments in treating complex conditions that have both neurological and metabolic components. This underscores the peptide's significance in bridging neurochemical, physiological, and behavioral research pursuits, offering a comprehensive understanding of pathways that are commonly dysregulated in diverse disorders.

How does CART (61-102) interact with other neuropeptides and neurotransmitters?

CART (61-102) interactions with other neuropeptides and neurotransmitters underscore its importance in neural regulation and signaling pathways. It serves as a dynamic modulator within the intricate neuronal networks that maintain homeostasis and respond to external stimuli. One prominent interaction is with the leptin and melanocortin systems, both crucial in energy balance and appetite regulation. CART (61-102) is found to exert orexigenic effects, working in concert with leptin to inhibit feeding. Leptin, a hormone predominantly produced by adipose cells, helps regulate energy balance by inhibiting hunger, and CART (61-102) amplifies this anorectic effect by acting downstream in the signaling pathway, reinforcing leptin signal transduction and enhancing the centrally mediated satiety effect.

Additionally, CART (61-102) influences dopaminergic pathways, particularly within the mesolimbic and nigrostriatal systems associated with reward and motivation. The modulation of dopamine release by CART (61-102) positions it as a crucial neuropeptide in addiction studies, highlighting its potential to alter reward circuitries often hijacked by addictive substances. This interaction is significant due to dopamine's pivotal role in reward, pleasure, and addiction processes, suggesting that CART peptides may modulate both natural and drug-induced reward mechanisms, potentially offering therapeutic avenues for treating addiction.

CART (61-102) also displays significant interaction with serotoninergic systems. Serotonin is a key neurotransmitter involved in mood regulation, and CART's modulatory effects on serotonin signaling pathways suggest its role in mood disorders such as depression and anxiety. The anxiolytic-like effects observed in preclinical models upon the administration of CART (61-102) hint at an intricate relationship with serotoninergic transmission, adding another dimension to its neuromodulatory scope.

In stress-related responses, CART (61-102) interacts with corticotropin-releasing factor (CRF), an essential component of the hypothalamic-pituitary-adrenal (HPA) axis. The interplay between CART (61-102) and CRF indicates a role in stress adaptation processes, which could translate into therapeutic strategies for stress-related ailments. These multidimensional interactions with various neurotransmitters and neuropeptides underscore the pivotal positioning of CART (61-102) within the physiological realm, revealing its potential in developing treatments for a range of neuropsychological and metabolic disorders through its regulatory capacity to balance different neural systems.

Can CART (61-102) be considered a target for developing new drug therapies?

The potential of CART (61-102) as a target for drug development is garnering significant interest due to its wide-ranging roles in physiological regulation and disease modulation. Its influence on appetite suppression makes it a highly attractive candidate for developing obesity treatments. Given the global rise in obesity-related conditions, there is a demand for novel therapies that can effectively aid in weight management. CART (61-102), through its anorectic effects, could potentially be harnessed to develop pharmacological agents that offer improved mechanisms for weight loss compared to current treatments, by directly modulating neuronal pathways involved in hunger control and satiety.

Furthermore, the involvement of CART (61-102) in addiction and reward pathways presents opportunities to develop therapeutic strategies targeting substance abuse disorders. Current treatments for addiction often have limited efficacy and significant side effects, underscoring the need for innovative approaches. By modulating dopaminergic pathways, a drug designed around CART (61-102) could offer a means to alter the reward mechanisms manipulated by addictive substances, providing a novel approach to treating addictions with potentially fewer side effects.

CART (61-102) is also being explored in the realm of psychiatric disorders such as anxiety and depression. Traditional treatments for these conditions, often focused on serotonin and dopamine modulation, may benefit from the complementary action of CART-targeted therapies. Its involvement in mood regulation pathways suggests that CART-based drugs might offer alternative or adjunct interventions for patients unresponsive to conventional antidepressants or anxiolytics, or for those who experience adverse reactions.

Moreover, targeting CART (61-102) could pave the way for advances in the treatment of stress-related disorders. With its role in modulating stress response pathways, drugs that mimic or enhance CART (61-102) signaling could potentially ameliorate symptoms related to chronic stress and anxiety disorders, promoting a balanced physiological stress response.

Despite these promising avenues, the development of CART (61-102)-based therapies remains in the early stages. More research is necessary to fully elucidate its mechanisms and to ensure the specificity and safety of such treatments. However, the potential of CART (61-102) as a drug target represents an exciting frontier in medical research, with the promise of innovative interventions for complex metabolic and neuropsychiatric conditions.

What are the roles of CART (61-102) in modulating stress and anxiety behaviors?

CART (61-102) has emerged as a significant player in modulating stress and anxiety-related behaviors, functioning within the complex neural networks that manage these responses. Stress and anxiety are mediated by intricate systems involving the hypothalamic-pituitary-adrenal (HPA) axis and various neurotransmitter systems. CART (61-102) peptides are expressed in brain regions integral to stress response, such as the hypothalamus and amygdala. Research indicates that upon exposure to stressors, CART (61-102) levels fluctuate, suggesting its active involvement in stress adaptation.

In animal models, administration of CART (61-102) has demonstrated anxiolytic-like effects, indicating that it may help mitigate anxiety. This can be attributed to its interaction with the serotoninergic system, where it likely modulates serotonin levels or receptor activity, contributing to the modulation of mood and anxiety. The peptide’s potential to alter the function of serotonin receptors directly or indirectly offers a clue into its capacity to manage anxiety states. This provides a physiological basis for considering CART (61-102)-based interventions as therapeutic options for anxiety disorders.

CART (61-102)'s involvement with the corticotropin-releasing factor (CRF), a primary stress hormone, indicates a role in the regulation of the HPA axis. By interacting with CRF, CART (61-102) may influence the secretion of adrenocorticotropic hormone (ACTH) and other stress-related hormones. This interaction is crucial, as a dysregulated HPA axis is often linked with chronic stress and anxiety disorders. Therefore, through this regulatory mechanism, CART (61-102) might contribute to maintaining homeostasis in stress responses, thereby supporting adaptive behavior under stress conditions.

The peptide also engages dopaminergic and noradrenergic pathways, both of which are critical to arousal and stress response. Modulation of these pathways by CART (61-102) could help explain its role in modifying the physiological and behavioral reactions to stress, potentially offering novel therapeutic angles for neuropsychiatric conditions characterized by stress dysregulation.

The versatility of CART (61-102) in engaging multiple neural networks highlights its potential as a modulatory agent in stress and anxiety. By influencing key neurotransmitter systems and interacting with stress-related hormones, it serves as a potential focal point for the development of treatments targeting stress-related disorders. Understanding its comprehensive roles opens pathways for CART (61-102)-centered strategies in managing stress and anxiety, providing hope for new therapeutic paradigms.

How might CART (61-102) influence future research directions in neuroscience?

CART (61-102) holds great promise for future research directions in neuroscience, primarily due to its intricate involvement in numerous neurobiological functions and disorders. A profound understanding of CART (61-102) could significantly influence the development of novel therapeutic strategies for treating a wide array of conditions ranging from metabolic to neuropsychiatric disorders. The peptide is implicated in appetite control, addiction, stress response, and mood regulation, each associated with significant health burdens, thus steering neuroscientific research towards more targeted approaches.

Emerging evidence regarding CART (61-102)'s role in energy homeostasis suggests that it could be pivotal in revolutionizing obesity research. With the global obesity epidemic, understanding how CART (61-102) regulates appetite and body weight is vital. Future research can focus on decoding its signaling pathways and interactions with other hormones like leptin and ghrelin, potentially leading to targeted interventions that offer new therapeutic options in weight management.

The peptide's influence on dopaminergic pathways makes it an exciting candidate for addiction research. By exploring how CART (61-102) modulates addiction pathways, researchers can develop a clearer picture of its role in reward mechanisms, leading to novel treatments for substance use disorders. This can also extend to understanding reward-related psychiatry issues, offering insights into conditions like compulsive gambling or overeating.

Concerning mood and anxiety disorders, CART (61-102)'s interactions with serotonin and stress hormones position it as a promising subject in psychopharmacology. Future research can delve into its potential as a biomarker or treatment target for anxiety, depression, and other mood disorders. This might enable the development of therapies that are more effective or have fewer side effects than current medications.

Additionally, CART (61-102) research could facilitate advances in neuroendocrinology, given its interactions with the HPA axis and other neuroendocrine pathways. Understanding these interactions could yield insights into complex conditions like chronic stress syndromes, potentially leading to groundbreaking therapeutic developments for stress-related disorders.

The scope of CART (61-102) in neuroscience is vast and largely untapped. By expanding research efforts, scientists can uncover the myriad of ways in which this peptide influences human physiology and behavior. This involves not only exploring its potential therapeutic applications but also understanding its fundamental roles in maintaining neurobiological homeostasis, ultimately contributing to an enriched understanding of brain function and its impact on overall health.
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