Taiy Chemical
Uroguanylin (human)
Synonym UROG_HUMAN
Species Human
Protein Accession P09429
Purity Greater than 98% as determined by SEC-HPLC and SDS-PAGE
Endotoxin Level Less than 1 EU/ug
Biological Activity Fully biologically active when compared to standard. The ED50 as determined by a cell proliferation assay using FRTL-5 cells is less than 1.0 ng/ml, corresponding to a specific activity of >1.0 × 10^6 IU/mg.
Expression System Escherichia coli
Fusion Tag None
Predicted Molecular Mass 10.4 kDa
Formulation Lyophilized from a 0.2 μm filtered solution of 20 mM PB, 150 mM NaCl, pH 7.2
Reconstitution It is recommended to reconstitute the lyophilized Uroguanylin in sterile 18MΩ-cm H₂O not less than 100 μg/ml, which can then be further diluted to other aqueous solutions.
Storage & Stability Lyophilized Uroguanylin although stable at room temperature for 3 weeks, should be stored desiccated below -18°C. Upon reconstitution Uroguanylin should be stored at 4°C between 2-7 days and for future use below -18°C. For long-term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please prevent freeze-thaw cycles.
FAQ
What is Uroguanylin and what role does it play in the human body?

Uroguanylin is a peptide hormone that plays a crucial role in the human body, primarily involved in regulating fluid and electrolyte balance. This peptide is part of the guanylin peptide family, which also includes guanylin and lymphoguanylin. Uroguanylin is mainly expressed in the intestinal epithelial cells and gets activated upon food intake. Once released into the bloodstream, it targets the kidney’s intestinal and renal epithelial cells, initiating a cascade of biochemical events significant to maintaining body fluid equilibrium. Uroguanylin functions through the receptor guanylate cyclase C (GC-C), found on the surface of the intestinal and renal epithelial cells. Upon binding to this receptor, uroguanylin activates it, resulting in increased production of cyclic guanosine monophosphate (cGMP). This secondary messenger influences the activity of ion channels and transporters, enhancing the excretion of sodium and chloride ions into the intestinal lumen and subsequently into urine. These actions help regulate blood pressure by promoting natriuresis, the excretion of sodium into urine, thus helping control blood volume and systemic blood pressure.

In addition to its primary role in fluid and electrolyte homeostasis, uroguanylin has been found to exhibit various other physiological functions. Recent studies suggest an involvement in body weight regulation. It is hypothesized that uroguanylin could influence appetite and energy expenditure by signaling satiety from the gut to the brain. Therefore, it might be considered a target for managing obesity and metabolic disorders. Moreover, uroguanylin’s capacity to maintain the balance of electrolytes in the gastrointestinal tract can affect local gut health, indirectly influencing digestive efficiency and gut flora composition. Understanding the complex actions of uroguanylin and its mechanisms opens new doors for therapeutic interventions in conditions like hypertension, heart disease, and metabolic disorders. Scientists continue to explore uroguanylin’s roles, enhancing our grasp on how intricately balanced processes within the body contribute to overall health.

How does Uroguanylin influence fluid and electrolyte balance in the body?

Uroguanylin exerts significant influence over fluid and electrolyte balance through its interaction with the receptor guanylate cyclase C (GC-C), which predominantly localizes in the intestines and kidneys. This peptide hormone modulates the function of epithelial cells responsible for regulating ionic gradients and fluid exchange. Initial secretion of uroguanylin is triggered by nutrient ingestion, prompting its release from intestinal endocrine cells into circulation. Its primary mechanism of action is through increasing intracellular cyclic guanosine monophosphate (cGMP) levels, which serve as a signaling molecule to mediate chloride and sodium ion transport across epithelial membranes.

Within the intestines, uroguanylin signaling facilitates chloride ion secretion and inhibits absorption of sodium ions, contributing to the osmotic flow of water into the gut lumen. This process aids in maintaining hydration and electrolyte balance as part of normal digestive processes. In the renal system, uroguanylin helps regulate sodium handling via nephron tubular structures, enhancing sodium excretion through natriuresis. By promoting the removal of excess sodium, uroguanylin indirectly controls blood volume and systemic blood pressure, functioning as a natural regulator against hypertension and salt retention disorders.

Furthermore, uroguanylin extends its impact to the modulation of other ion exchanges, including bicarbonate transportation, essential in acid-base homeostasis. Bicarbonate plays a key role in bicarbonate recovery within renal proximal tubules and assists in neutralizing acidic compounds in the gastrointestinal tract, promoting pH equilibrium and favorable conditions for enzymatic functions. The ultragovernmental action of uroguanylin not only influences electrolyte and fluid levels but also has potential implications for weight management. Some studies suggest that cGMP signaling pathways, initiated by uroguanylin, may integrate messages related to appetite control and energy expenditure between the gut and central nervous systems, adding complexity to its physiological roles.

In summary, the role of uroguanylin extends across maintaining salt and fluid homeostasis, contributing to healthy blood pressure levels, and potentially affecting metabolic processes. As research evolves, understanding the breadth of uroguanylin’s influences could provide key insights into its therapeutic benefits in chronic health conditions like cardiovascular diseases and obesity.

Is Uroguanylin linked to any potential therapeutic applications?

Uroguanylin holds promise in several therapeutic applications due to its regulatory functions on fluid and electrolyte balance, as well as its broader physiological effects that are continually being elucidated. Its ability to modulate sodium and fluid levels makes it a potential therapeutic target in treating hypertension and associated cardiovascular disorders. By promoting natriuresis and diuresis, uroguanylin analogs or modulators may help manage high blood pressure naturally, reducing the risk of adverse effects common in conventional antihypertensive medications. Moreover, targeting this pathway could offer a more physiological approach to controlling salt-sensitive hypertension, where traditional treatments might fall short.

Emerging evidence also highlights the potential of uroguanylin in addressing metabolic disorders, including obesity and type 2 diabetes. Some studies suggest that by influencing the guanylate cyclase C pathway, uroguanylin may play a role in appetite regulation and energy homeostasis. Experimental data indicate that this peptide could interact with satiety signaling, thereby reducing food intake and modulating body weight. Thus, leveraging uroguanylin could pave the way toward new weight management therapies, which are in strong demand given the prevalence of obesity and its associated health burdens.

Beyond metabolic conditions, uroguanylin has shown promise in gastrointestinal health. Its role in maintaining intestinal ion transport and mucosal hydration suggests potential applications in treating intestinal disorders. Conditions such as chronic constipation or certain forms of irritable bowel syndrome (IBS) might benefit from medications that modulate the activity of uroguanylin to enhance fluid secretion and relieve symptoms. Indeed, drugs that mimic uroguanylin's effects are under investigation or development, offering hope for patients with limited treatment options.

Lastly, uroguanylin is being explored for its potential applications in oncology. The guanylate cyclase C receptor, targeted by uroguanylin, is expressed in various cancers, including colorectal cancer. Researchers are studying if uroguanylin or its analogs could be used to inhibit cancer cell proliferation or serve as biomarkers for specific cancer types. The development of these therapeutic avenues exemplifies the promising nature of uroguanylin in medical advancements.

In conclusion, while uroguanylin is primarily recognized for its role in fluid and electrolyte regulation, its potential in therapeutic applications spans cardiovascular, metabolic, gastrointestinal, and oncologic fields. Ongoing research is essential for understanding its full therapeutic potentials and limitations, providing insight that could revolutionize treatments for various conditions.

How does Uroguanylin interact with other hormones or systems in the body?

Uroguanylin interacts with various systems and hormones in the body, primarily through its signaling pathways that modulate fluid, electrolyte balance, and metabolic processes. As a ligand for the guanylate cyclase C (GC-C) receptor, located mainly on the intestinal and renal epithelial cells, uroguanylin's action involves the generation of cyclic guanosine monophosphate (cGMP), a secondary messenger that has broad physiological implications. This signaling cascade indicates that uroguanylin intersects with numerous other hormonal and regulatory pathways, influencing bodily functions on multiple levels.

Foremost, uroguanylin impacts the renin-angiotensin-aldosterone system (RAAS), a key player in fluid and electrolyte homeostasis. By promoting natriuresis, or the excretion of sodium in urine, uroguanylin serves as a counterbalance to the sodium-retentive actions of aldosterone within the RAAS. This interaction helps regulate blood pressure and maintain volume homeostasis, offering a natural countermeasure to hypertensive states that involve hyperaldosteronism. Additionally, modulation of sodium and fluid retention is linked to uroguanylin's impact on atrial natriuretic peptide (ANP), a hormone produced by the heart’s atria that works synergistically with uroguanylin to lower blood pressure.

Uroguanylin also has interactions with the central nervous system, particularly through its potential influence on appetite and energy regulation. Some studies propose that uroguanylin can signal through the vagus nerve, transmitting satiety signals from the gut to the brain, thereby interfacing with the neuronal circuits governing hunger and energy balance. This dietary hormone signaling aligns with metabolic hormones such as leptin and ghrelin, which are central to energy homeostasis and body weight regulation.

Furthermore, recent research suggests uroguanylin's involvement in glucose metabolism, implicating cross-talk with insulin signaling pathways. By enhancing intestinal blood flow and nutrient absorption via cGMP signaling, uroguanylin may indirectly affect glucose levels, although the precise mechanisms are still being studied. This interaction could create potential intersections with diabetic treatments, where uroguanylin’s pathways might be targeted to modulate glycemic control.

Moreover, uroguanylin engages with gut microbiota, an emerging area of investigation, where the modulation of intestinal environment and pH by uroguanylin may affect microbial composition, potentially influencing metabolic health and diseases like obesity or inflammatory bowel disease. The complex biome and its secretions further entail networked interactions involving uroguanylin, suggesting that hormonal balance, intestinal health, and microbial environments are deeply interwoven.

In conclusion, the interactions of uroguanylin with other systems and hormones underscore its integrative role in maintaining physiological balance. From fluid retention to metabolic regulation, these intersections demonstrate the complex networks that uroguanylin is a part of, highlighting the hormone's potential as a therapeutic target in managing disorders ranging from hypertension to metabolic syndromes. Comprehensive understanding and exploration of these interactions could lead to new insights and innovations in medical treatments.

What are the clinical implications of Uroguanylin in disease management?

The clinical implications of uroguanylin in disease management are expansive and currently a subject of intense research. Due to its physiological role in maintaining fluid, electrolyte balance, and potentially influencing energy regulation, uroguanylin presents various pathways for therapeutic exploration across a spectrum of diseases. One of the most prominent areas of research is its application in managing hypertension and related cardiovascular disorders. Uroguanylin, by promoting natriuresis and diuresis, provides a mechanism for reducing blood volume and subsequent blood pressure. Understanding the regulatory role of uroguanylin in blood pressure homeostasis could yield novel treatments for resistant hypertension, particularly in salt-sensitive individuals where conventional medications might be ineffective.

In addition to its cardiovascular applications, uroguanylin is being investigated for its potential role in treating metabolic disorders such as obesity and type 2 diabetes. While its complete mechanisms in these conditions are still being unraveled, initial studies suggest that uroguanylin might influence appetite regulation and energy homeostasis. If this hormone can signal satiety to central nervous systems effectively, therapies aimed at mimicking or enhancing uroguanylin’s action could serve as viable interventions in managing obesity. Additionally, improving metabolic efficiency and glucose metabolism through these pathways could offer new avenues for balancing insulin resistance and aiding diabetic treatments.

Uroguanylin is also significant in gastrointestinal disease management. Its effect on intestinal fluid secretion positions it as a candidate treatment for disorders like constipation-predominant irritable bowel syndrome (IBS) and possibly other forms of chronic constipation. By regulating fluid movement and ion transport in the intestine, medications that replicate uroguanylin’s effects could provide symptomatic relief for patients with these gastrointestinal conditions, improving quality of life where limited options exist.

Further, potential roles of uroguanylin in cancer therapy are being explored, particularly given its expression through guanylate cyclase C receptors present in certain cancers such as colorectal cancer. Uroguanylin or its analogs might serve as biologic markers for cancer or even as direct inhibitors of tumor growth through pathways still being studied.

Lastly, exploring uroguanylin's impact on gut microflora represents another frontier, as shifts in microbial populations influence both metabolic and immune health. Therapies modulating uroguanylin levels could be designed to adjust microbial composition favorably, which may impact inflammatory diseases, obesity, and diabetes.

While the full clinical potentials of uroguanylin remain to be comprehensively mapped, its multi-dimensional role in diseases provides a promising landscape for novel treatment options. The continued elucidation of its biological interactions, mechanisms, and effects can pave the way toward more precise, effective therapeutic strategies that leverage uroguanylin's natural regulatory functions. Thus, research into uroguanylin highlights its potential as a cornerstone in managing a variety of chronic health conditions.
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