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.