Taiy Chemical
Cholecystokinin Octapeptide (1-5) (desulfated)
Synonym CCK-8 (1-5) (desulfated)
Species Human
Protein Accession P06307
Purity > 95%
Endotoxin Level < 1.0 EU per μg
Biological Activity Not determined
Expression System Chemical Synthesis
Fusion Tag None
Predicted Molecular Mass 751.88 Da
Formulation Supplied as a lyophilized powder
Reconstitution Centrifuge vial before opening. Reconstitute in distilled water or aqueous buffer containing 0.1% BSA to a concentration of 0.1-1.0 mg/ml.
Storage & Stability Store lyophilized peptide at -20°C. Reconstituted peptide should be stored at -20°C or lower.
FAQ
What is Cholecystokinin Octapeptide (1-5) (desulfated) and how does it function in the body?

Cholecystokinin Octapeptide (1-5) (desulfated), often referred to simply as CCK, is a peptide that plays a significant role in the digestive system. It is a derivative of the natural hormone cholecystokinin (CCK), which is produced in the small intestine and acts as a critical mediator in digestion and appetite regulation. CCK is usually released in response to food intake, especially when fats and proteins enter the duodenum, the first segment of the small intestine. Although Cholecystokinin Octapeptide (1-5) is a modified form lacking the sulfate group, it still retains some of the important functional properties of native CCK, albeit with altered bioactivity.

In the digestive system, CCK binds to receptors in the pancreas and gallbladder, facilitating the release of digestive enzymes and bile, respectively. These substances are essential for the breakdown and absorption of nutrients, notably fats. Additionally, CCK contributes to the slowing of gastric emptying, which gives the digestive system more time to process the ingested food. This delay in emptying also leads to the sensation of fullness, which is why CCK has been studied in the context of weight management and appetite regulation. While Cholecystokinin Octapeptide (1-5) (desulfated) does not mimic these effects exactly due to its structural differences, it serves as a tool for research into the precise mechanisms and potential applications of CCK-like activity.

Beyond digestion, there is interest in CCK signaling pathways in the brain, where it potentially influences mood and anxiety. CCK receptors are distributed in various brain regions and are involved in modulating neurochemical signaling. Despite being a gastrointestinal hormone, its reach extends into the central nervous system, suggesting that compounds like Cholecystokinin Octapeptide (1-5) could have broader implications in neuroscience research. Understanding the desulfated form can help delineate the specific actions that sulfate groups have on receptor binding and function, advancing our comprehension of molecular-signaling cascades.

In summary, while Cholecystokinin Octapeptide (1-5) (desulfated) itself is primarily leveraged in research settings, it is a valuable tool for elucidating the intricate roles of CCK in both the peripheral digestive systems and the central nervous system. Its applications in studying digestion, appetite regulation, and potential neural implications make it an exciting area of ongoing scientific exploration.

How is Cholecystokinin Octapeptide (1-5) (desulfated) utilized in research settings?

Cholecystokinin Octapeptide (1-5) (desulfated) is primarily used as a research tool in scientific studies exploring the physiological and biochemical roles of cholecystokinin and related peptides. This modified peptide enables scientists to investigate the specific contributions of sulfate groups in natural cholecystokinin and how they impact its biological activities. Its utilization in research settings is diverse, spanning studies in digestive physiology, metabolic regulation, neurobiology, and even in the development of potential therapeutics.

In digestive physiology research, scientists employ Cholecystokinin Octapeptide (1-5) (desulfated) to better understand the hormone's role in digestive enzyme secretion and gallbladder contraction. By comparing the functional outcomes of the desulfated form to the native hormone, researchers can discern how sulfation affects receptor binding affinity and subsequent physiological responses. This knowledge enhances our comprehension of digestion processes and could lead to novel treatment strategies for disorders such as pancreatitis or gallbladder disease. Additionally, insights into CCK-driven gastric motility adjustments provide avenues for addressing functional gastrointestinal disorders, such as irritable bowel syndrome.

Metabolic research also benefits immensely from utilizing Cholecystokinin Octapeptide (1-5) (desulfated). CCK's ability to induce satiety and reduce food intake is of great interest in the context of obesity and weight management. By studying the desulfated peptide, researchers can parse out the specific signaling pathways involved in appetite regulation and energy balance. This work could inform the development of novel weight loss drugs or therapies addressing metabolic diseases. The potential non-digestive actions of CCK in regulating insulin secretion and glucose metabolism further expand the scope of metabolic research applications.

In neurobiology, Cholecystokinin Octapeptide (1-5) (desulfated) serves as an investigative tool to explore the brain's CCK receptor systems. The distribution of these receptors in areas related to mood and anxiety regulation presents intriguing lines of inquiry for mental health research. By observing the effects of the desulfated peptide, scientists gain insight into how chemical modifications at the molecular level affect neuronal activity and behavior. These studies might inform future psychiatric medication development, particularly those aiming to address anxiety disorders or depressive states.

The desulfated peptide's role in advancing pharmacological research should also be highlighted. By synthesizing and manipulating peptide analogs like Cholecystokinin Octapeptide (1-5), developers can explore new compounds that may mimic or antagonize natural CCK activity for therapeutic purposes. The desulfation provides a unique comparison point to probe critical binding interactions at receptor sites, essential for drug discovery and optimization processes.

In conclusion, Cholecystokinin Octapeptide (1-5) (desulfated) is an indispensable tool for scientific research across multiple disciplines. Its utility in elucidating the fine details of CCK's role in digestion, metabolism, brain function, and therapeutic applications underscores its value in advancing both fundamental biological knowledge and applied medical sciences.

What makes Cholecystokinin Octapeptide (1-5) (desulfated) distinct from its naturally occurring counterpart?

Cholecystokinin Octapeptide (1-5) (desulfated) differs from its naturally occurring counterpart primarily through the absence of a sulfate group. This structural modification, while seemingly minor, significantly influences the peptide's biochemical properties, receptor binding capabilities, and subsequent physiological effects. A closer examination of these differences provides insight into the intricate role that sulfation plays in peptide hormone activity and receptor interaction.

In its natural form, cholecystokinin plays a crucial role in regulating digestive processes, notably by stimulating enzyme secretion from the pancreas and contracting the gallbladder to release bile. These actions are mediated through CCK receptors, which have a high affinity for the sulfated version of the peptide. The presence of the sulfate group enhances the hormone's hydrophilicity and promotes specific binding conformations that are highly favorable for interaction with these receptors. Consequently, the removal of this sulfate group in the desulfated form affects the binding dynamics and potency of the peptide.

The distinct receptor interactions of Cholecystokinin Octapeptide (1-5) (desulfated) are a central focus of scientific investigation. Since desulfated peptides typically have a reduced binding affinity for CCK receptors, they serve as useful tools for dissecting the relationship between molecular structure and receptor engagement. Researchers utilize the desulfated peptide to control and manipulate signaling pathways, elucidating the contribution of specific chemical groups to the hormone's overall activity. This understanding provides a foundation for exploring receptor function, ligand specificity, and the development of selective receptor modulators.

Moreover, the desulfated form allows for a better understanding of the non-classical roles of CCK beyond digestion. In the central nervous system, CCK receptors are implicated in modulating anxiety, pain perception, and satiety signals. The altered binding characteristics of Cholecystokinin Octapeptide (1-5) (desulfated) offer a unique perspective on these pathways. Studying how this version of the peptide interacts with brain receptors can yield valuable insights into the structural requirements for neuronal signaling and may highlight new therapeutic targets for neurological disorders.

In terms of biochemical research, the synthesis of Cholecystokinin Octapeptide (1-5) (desulfated) benefits from its stability and ease of manipulation compared to its sulfated counterpart. This stability makes it a preferred candidate for long-term studies and bioanalytical applications. Researchers can use this peptide to better understand degradation pathways, receptor turnover, and the systemic distribution of cholecystokinin-like peptides in biological systems.

In summary, the distinctiveness of Cholecystokinin Octapeptide (1-5) (desulfated) lies in its structural variance and the consequent effects on physiological and receptor-specific activities. This desulfated derivative not only provides a lens through which we can explore fundamental biological processes but also advances our capabilities in developing targeted therapeutic interventions. The study of this peptide illustrates the profound impact that subtle molecular modifications can have on a hormone's function and its potential applications in both health and disease contexts.

What are the potential applications of research involving Cholecystokinin Octapeptide (1-5) (desulfated)?

Research involving Cholecystokinin Octapeptide (1-5) (desulfated) holds numerous potential applications across various scientific and medical fields. This derivative of the natural CCK hormone serves as a vital tool for investigating basic biological mechanisms and holds promise for advancing therapeutic developments. Potential applications extend from enhancing our understanding of gastrointestinal physiology to exploring neurological pathways and creating innovative treatments for metabolic disorders.

One key application lies in the realm of digestive health and disease. Understanding how CCK and its derivatives influence pancreatic enzyme secretion and gall bladder contraction is paramount in treating digestive disorders such as chronic pancreatitis and gallstones. The study of Cholecystokinin Octapeptide (1-5) (desulfated) can elucidate the pathways through which the hormone modulates these processes, potentially leading to novel interventions or therapeutics. Moreover, exploring its role can aid in developing treatments that mimic or enhance the natural hormone's effects, providing relief for patients with impaired digestive functions.

Research into the peptide's influence on appetite control and metabolic regulation also presents significant applications, particularly in addressing the growing global challenge of obesity. Investigations into how the desulfated form affects appetite, energy expenditure, and satiety hormones can inform the development of appetite suppressants or weight management therapies. This application is critically important as obesity is linked to various chronic conditions, including heart disease, diabetes, and certain cancers. Cholecystokinin's role in regulating energy balance and meal termination can form the basis for creating new drugs targeting these pathways, offering more effective weight loss solutions.

Moreover, Cholecystokinin Octapeptide (1-5) (desulfated) has significant implications for neuroscience research. The peptide's interaction with brain CCK receptors involved in mood regulation, anxiety, and possibly pain perception provides grounds for exploring novel treatments for psychiatric and neurological disorders. Understanding how this derivative affects brain receptor pathways opens potential for developing therapeutics for anxiety and mood disorders, which are prevalent and often difficult to manage. The peptide could also serve as a model for studying the neurobiological underpinnings of pain, paving the way for better analgesic drugs.

Another promising application lies in drug development and structure-activity relationship studies. By manipulating the peptide structure and analyzing the effects of desulfation, researchers can gain insights into receptor specificity and ligand-receptor interactions. This knowledge is crucial for designing new compounds with improved efficacy and reduced side effects, leading to the development of more refined pharmacological agents.

Additionally, Cholecystokinin Octapeptide (1-5) (desulfated) supports biomarker discovery. As researchers map out its roles and effects in biological processes, there arises an opportunity to identify new biomarkers for diseases related to digestion, metabolism, and mental health. These biomarkers can be pivotal for early diagnosis, disease monitoring, and personalized medicine approaches.

In conclusion, the research and applications of Cholecystokinin Octapeptide (1-5) (desulfated) are vast and impactful, extending well beyond traditional boundaries of peptide study. Through continued exploration of its roles and mechanisms, this desulfated peptide stands to offer transformative insights and solutions in health and disease, underscoring the critical importance of ongoing scientific inquiry in this area.

What are the challenges researchers face when working with Cholecystokinin Octapeptide (1-5) (desulfated)?

Working with Cholecystokinin Octapeptide (1-5) (desulfated) presents researchers with a myriad of challenges, reflective of the intricate nature of peptide research and the complexities of deciphering biological pathways. One of the primary hurdles is related to the physiological relevance and translation of in vitro findings to in vivo systems. While in vitro assays provide controlled environments where cellular responses to the peptide can be thoroughly observed and measured, these conditions often do not fully replicate the multifaceted interactions occurring within living organisms. Discrepancies between in vitro and in vivo data can pose significant challenges in drawing accurate conclusions about the peptide's biological roles.

Structurally, the absence of the sulfate group in desulfated peptides like Cholecystokinin Octapeptide (1-5) raises questions about receptor specificity and binding affinity. Researchers must grapple with understanding the influence this desulfation has on the peptide's interaction with CCK receptors. This structural modification can lead to altered binding kinetics and efficacy, complicating efforts to attribute specific physiological effects to the peptide. Identifying and characterizing these interactions necessitates sophisticated experimental setups and can involve extensive trial and error to refine methods and validate results.

Another challenge lies in analyzing the systemic effects of administering Cholecystokinin Octapeptide (1-5) (desulfated). As the peptide can potentially influence various biological pathways—ranging from digestion to neurological functions—isolating specific mechanisms is inherently complex. Research must be meticulously designed to control for confounding variables and ensure that observed effects are directly attributable to the peptide itself. This complexity is further heightened in vivo, where the peptide might cross-react with unintended targets, necessitating rigorous due diligence in experimental controls and validation analyses.

Moreover, peptide stability poses a significant hurdle in research settings. Peptides are inherently susceptible to degradation by proteolytic enzymes, which can compromise the integrity of experimental results. Ensuring stability often requires careful consideration of storage conditions, formulation, and the use of stabilizing agents—adding layers of complexity to experimental designs and logistics.

The scalability of producing Cholecystokinin Octapeptide (1-5) (desulfated) for large-scale studies can also be challenging. Peptide synthesis and purification need to be optimized for yield, purity, and cost-effectiveness, especially when transitioning from laboratory-scale to broader applications. Variations in synthesis techniques can lead to inconsistencies, affecting reproducibility and reliability of research outcomes.

Financial constraints also contribute to the challenges faced by researchers. Conducting comprehensive studies involving Cholecystokinin Octapeptide (1-5) (desulfated), particularly those incorporating advanced biochemical and pharmacological techniques, requires substantial funding and resources. Securing funding becomes competitive, often contingent upon demonstrating significant preliminary data and potential impact.

Finally, ethical considerations, especially in translational research involving human subjects, introduce another layer of complexity. Ensuring that research progresses responsibly and with consideration of safety is crucial, necessitating stringent adherence to ethical guidelines and regulatory frameworks.

In summary, while research involving Cholecystokinin Octapeptide (1-5) (desulfated) is fraught with challenges encompassing experimental design, structural complexities, stability issues, and broader ethical and financial concerns, it remains a crucial and promising field. Addressing these challenges with innovation and meticulous scientific rigor is essential for advancing our understanding of this peptide's diverse roles and potential therapeutic applications.

What future directions could research into Cholecystokinin Octapeptide (1-5) (desulfated) take?

As the potential applications and impacts of Cholecystokinin Octapeptide (1-5) (desulfated) continue to unfold, several promising directions for future research become apparent. These directions encompass both the expansion of fundamental scientific knowledge and the exploration of translational and therapeutic innovations.

One compelling direction involves further elucidation of the peptide's role in appetite regulation and metabolic pathways. Continued investigation into how Cholecystokinin Octapeptide (1-5) influences energy balance and nutrient absorption could provide deeper insights into its potential as a target for anti-obesity therapies. With obesity rates climbing globally, research that advances understanding of appetite suppression and energy expenditure mechanisms holds immense public health relevance. Future studies might focus on bridging in vitro findings with clinical research, testing the peptide's effects on satiety and weight management in human trials.

Additionally, given the peptide's interactions within neurological pathways, future research could delve into the implications for mental health and psychiatric disorders. Exploring Cholecystokinin Octapeptide (1-5)'s effects on mood and anxiety regulation at a molecular level could reveal novel targets for pharmaceutical development. Research might expand into neuroimaging and electrophysiological studies to observe real-time brain activity changes following peptide administration, thereby unmasking its potential influence on neural networks implicated in emotional regulation.

The structural modification aspect of Cholecystokinin Octapeptide (1-5) (desulfated) also offers fertile ground for future investigations into peptide engineering. Building on our understanding of the relationship between peptide structure, receptor affinity, and functional outcome can inform the rational design of new compounds with enhanced specificity and efficacy. This area poses interesting possibilities for designing custom peptides tailored for specific receptor interactions, contributing to the burgeoning field of peptide-based therapeutics.

Moreover, the peptide's utility in biomarker discovery studies could be expanded, supporting early disease detection and personalized treatment approaches. Future research might identify novel biomarkers related to CCK pathways by investigating differential expression and signaling patterns associated with Cholecystokinin Octapeptide (1-5) (desulfated) in various tissues. This could pave the way for precision medicine applications, wherein interventions are fine-tuned based on individual biomarker profiles.

Exploration of combinations with other hormones or pharmaceutical agents presents another direction for advancing research. Investigating synergistic effects between Cholecystokinin Octapeptide (1-5) and other hormonal regulators of metabolism or mood could uncover compound treatment strategies that maximize therapeutic benefits while minimizing side effects. Such combination therapies might offer a multifaceted approach to treating complex disorders like obesity, diabetes, or mood disorders.

Collaborations across multidisciplinary fields—such as bioinformatics, synthetic biology, and pharmacology—will be crucial in pursuing these future directions. Integrating computational modeling, for instance, might accelerate the understanding of peptide interactions at atomic and molecular levels, optimizing design and application strategies. Meanwhile, advancements in synthetic biology could facilitate the production of more stable peptide analogs, enhancing research efficiency and scalability.

In conclusion, the future directions for research involving Cholecystokinin Octapeptide (1-5) (desulfated) are vast and varied, promising expansive contributions to scientific knowledge and clinical practice. By fostering continued exploration and innovation in these areas, researchers stand to unlock further potential in understanding complex biological systems and developing meaningful therapeutic tools.
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