Synonym |
pTH (1-31) amide (human) |
Species |
Human |
Protein Accession |
N/A |
Purity |
Greater than 95% |
Endotoxin Level |
Less than 0.1 ng/µg |
Biological Activity |
N/A |
Expression System |
Chemical synthesis |
Fusion Tag |
N/A |
Predicted Molecular Mass |
N/A |
Formulation |
Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA |
Reconstitution |
It is recommended to reconstitute the lyophilized pTH (1-31) in sterile 18MΩ-cm H2O not less
than 100μg/ml, which can then be further diluted to other aqueous solutions. |
Storage & Stability |
Lyophilized pTH (1-31) although stable at room temperature for 3 weeks, should be stored
desiccated below -18°C. |
FAQ
What is pTH (1-31) amide (human), and what role does it play in human health?
Parathyroid hormone
(PTH) is a critical regulator of calcium and phosphate metabolism in the body. Produced by the
parathyroid glands, it plays a pivotal role in maintaining serum calcium levels within a narrow
physiological range. The pTH (1-31) amide is a peptide fragment of the full-length PTH molecule,
specifically consisting of the first 31 amino acids modified at the C-terminus to include an amide
group. This modification is significant because the N-terminal region of PTH is primarily responsible
for its biological activity, meaning that pTH (1-31) amide retains many of the skeletal effects of the
full-length hormone.
In human health, PTH's primary actions are on the bones, kidneys, and,
indirectly, the intestines. It stimulates osteoclasts in the bones to increase bone resorption,
releasing calcium and phosphate into the bloodstream. In the kidneys, PTH increases calcium reabsorption
in the distal tubules while promoting phosphate excretion. This finely tuned balance is crucial for
various physiological processes, including nerve conduction, muscle contraction, and blood coagulation.
Additionally, PTH facilitates the conversion of vitamin D to its active form in the kidneys, which then
enhances intestinal absorption of calcium and phosphate.
Understanding the specific role of pTH
(1-31) amide involves appreciating its potential therapeutic implications. As a potent fragment of PTH,
it could provide benefits in conditions where bone health is compromised. For instance, osteoporosis, a
condition characterized by bone density loss and increased fracture risk, could be managed more
effectively with treatments targeting bone regeneration and reducing further bone resorption. The action
of pTH (1-31) amide, with its ability to stimulate bone formation without the simultaneous catabolic
effects, is a promising area for research and therapeutic development. Thus, dissecting the role of this
peptide in human health not only enhances our understanding of PTH’s broader biological functions but
also points toward innovative treatments for metabolic bone diseases.
How is pTH (1-31) amide
(human) used in medical research?
In medical research, pTH (1-31) amide (human) serves as a
powerful tool for exploring various aspects of bone biology and calcium homeostasis. Its specific
configuration makes it an interesting candidate for studying PTH’s primary functions independent of its
full-length counterpart. The pTH (1-31) amide is often employed to examine the anabolic effects of PTH
on bone formation, distinct from its resorptive activities, which are appreciated in the context of
managing osteoporosis and other bone degenerative diseases. Researchers are particularly interested in
this fragment due to its capacity to promote osteoblastic activity, leading to new bone matrix
formation.
One area where pTH (1-31) amide is profoundly impactful is in the development of new
osteoporosis treatments. Traditional therapies often focus on inhibiting bone resorption, which, while
beneficial, do not address the deficit in bone formation. The ability of pTH (1-31) amide to stimulate
osteoblasts and enhance bone mass represents a paradigm shift toward anabolic treatment strategies that
not only halt bone loss but actively rebuild bone. This is crucial for developing therapeutics that can
improve bone density and structural integrity more holistically.
Moreover, pTH (1-31) amide is
also used to delineate the mechanisms of PTH receptor interactions. The understanding of ligand-receptor
dynamics is fundamental for the design of receptor-selective drugs that can maximize therapeutic
benefits while minimizing side effects. These insights are critical, especially for patients who might
be sensitive to the hypercalcemic effects of full-length PTH treatments, by selectively activating
pathways that enhance bone formation without eliciting significant hypercalcemia.
In addition to
these areas, the use of pTH (1-31) amide in research extends to evaluating its potential in addressing
hypoparathyroid conditions. Here, maintaining an anabolic environment without excessive calcium
mobilization can significantly enhance patient outcomes. With ongoing research, the nuanced
understanding provided by studies involving pTH (1-31) amide continues to propel forward the
possibilities for tailored, effective treatments in endocrinology and bone health.
What are the
potential benefits of pTH (1-31) amide (human) in treating osteoporosis?
Osteoporosis is a
prevalent bone disease characterized by decreased bone mass and structural deterioration, increasing
fracture risk. Traditional treatment modalities primarily focus on inhibiting bone resorption; however,
these approaches do not facilitate new bone formation, a necessary component for restoring bone health
in osteoporotic patients. Here is where pTH (1-31) amide (human) shows promise. This peptide fragment
holds the potential for a fundamentally different treatment approach—an anabolic therapy that encourages
new bone growth, providing a substantial benefit over existing therapies.
The mechanism by which
pTH (1-31) amide exerts its beneficial effects primarily involves stimulating osteoblast activity.
Osteoblasts are the cells responsible for bone formation, synthesizing new bone matrix, and facilitating
mineralization. By actively promoting osteoblastic function, pTH (1-31) amide can help rebuild bone
architecture, thereby increasing bone mass and strength. This not only counteracts the bone loss
associated with osteoporosis but also fortifies skeletal integrity, reducing the likelihood of
fractures, which are a significant concern.
Furthermore, clinical research suggests that pTH
(1-31) amide has a dual role of stimulating bone formation without proportionately increasing bone
resorption, as seen with full-length PTH or other anabolic treatments. This selective stimulation is
particularly critical for patients who need bone density improvement without experiencing adverse
hypercalcemic side effects. By providing an improved safety profile, pTH (1-31) amide stands out as a
potential therapy, especially for patients with underlying conditions that may predispose them to
calcium metabolism disorders.
Additionally, the benefit of using pTH (1-31) amide in treating
osteoporosis extends to potential improvements in bone quality. Beyond mere increases in bone mineral
density (BMD), enhancing the quality of bone microarchitecture and the toughness of bone are essential
for reducing fracture risks. The peptide’s influence on collagen arrangement and mineral distribution in
the bone matrix could markedly improve these quality parameters, leading to more significant clinical
outcomes than those achievable by simply mitigating bone loss.
These multifaceted benefits
underscore the transformative potential of pTH (1-31) amide as part of osteoporosis management. With its
focus on bone building rather than merely slowing bone breakdown, it aligns with therapeutic goals aimed
at restoring natural bone strength and durability, offering hope for improved quality of life for
individuals at risk for or suffering from osteoporosis.
How does pTH (1-31) amide (human) differ
from other parathyroid hormone treatments?
The pTH (1-31) amide (human) differs from other
parathyroid hormone treatments in several critical ways that pertain to its structure, mechanism of
action, and therapeutic effects, particularly in the context of bone health management. At the
structural level, pTH (1-31) amide represents a truncated form of the full parathyroid hormone,
consisting of the first 31 amino acids of the polypeptide, modified at the C-terminus to form an amide.
These modifications provide it the ability to act selectively within the body, targeting specific
receptor-mediated pathways that provide its therapeutic effect.
Full-length PTH or other extended
forms of the hormone usually stimulate both anabolic and catabolic pathways. While beneficial for
enhancing bone formation, this dual action often results in increased bone resorption as well, which can
lead to a less-than-ideal therapeutic profile for certain patients. Conversely, pTH (1-31) amide’s
shorter structure and targeted receptor interactions predominantly stimulate osteoblastic activity
without a commensurate increase in osteoclastic activity. This results in a net anabolic effect—more
bone formation—as opposed to a simultaneous stimulation of bone resorption that might counteract gains
in bone density.
From a pharmacodynamic perspective, this selective action is highly desirable in
patients where bone density preservation and increase are critical, such as those with osteoporosis.
This makes pTH (1-31) amide an attractive candidate for developing therapeutics aimed at enhancing bone
mass and structural integrity while minimizing adverse effects such as hypercalcemia, a common concern
in treatments involving longer forms of parathyroid hormone or its analogs.
The differences
extend to administration strategies and patient compliance as well. The selective and targeted nature of
pTH (1-31) amide could potentially translate into dosing advantages, where lower doses achieve the
desired outcome, improving patient adherence by reducing complexity in treatment regimens. This is vital
in long-term management scenarios, where consistent therapeutic engagement is crucial for
success.
Such distinct characteristics of pTH (1-31) amide not only differentiate it from other
forms of parathyroid hormone treatments but also open new avenues for its application beyond where
traditional PTH analogs are employed. It highlights the peptide's potential for broader use in treating
various metabolic or degenerative bone conditions, providing a novel approach that leverages its unique
mechanism, efficacy, and safety profile.
What are the safety considerations associated with using
pTH (1-31) amide (human)?
When considering the use of pTH (1-31) amide (human) for therapeutic
applications, understanding its safety profile is of paramount importance. One of the notable advantages
of this peptide is its selective mechanism of action. Because it predominantly stimulates bone formation
without significantly increasing bone resorption, the risk of hypercalcemia—a common side effect
associated with general PTH therapies—is reduced. Hypercalcemia can cause various symptoms and
complications, such as muscular weakness, fatigue, and in severe cases, cardiac arrhythmias. Therefore,
the reduced impact on calcium mobilization is a significant safety benefit of pTH (1-31)
amide.
However, as with any hormonal treatment, potential risks need to be carefully monitored.
The administration of hormones or hormone-like substances can have systemic effects, where unintended
stimulation of pathways can occur. For pTH (1-31) amide, while the risk is minimized compared to
full-length PTH treatments, vigilance in monitoring patients for signs of hypercalcemia is still
warranted, particularly in those with underlying health conditions affecting calcium metabolism or renal
function.
Moreover, long-term use of anabolic agents, even those selective for osteoblasts,
requires consideration given the delicate balance of bone remodeling processes. Excessive promotion of
bone formation without matched resorption can, in some cases, lead to aberrant bone growth or
alterations in bone quality. These concerns necessitate ongoing research and careful clinical planning,
including periodic bone density assessments to ensure balanced bone turnover is
maintained.
Patient-specific factors also play a crucial role in determining the safety and
efficacy of pTH (1-31) amide treatments. Medical history, concurrent medications, and pre-existing
conditions all influence therapeutic decisions. For instance, patients with severe kidney disease may
face challenges related to calcium handling, necessitating tailored approaches to treatment and more
rigorous monitoring of physiological responses to pTH (1-31) amide.
Finally, potential allergic
reactions and injection site reactions are standard safety considerations for any peptide-based
treatment administered subcutaneously. While such occurrences are generally rare and mild, they must be
accounted for when planning a patient’s treatment regimen. Educating patients about the signs of adverse
reactions and regularly reviewing their condition during follow-up appointments is essential to managing
such risks effectively.
Thus, while pTH (1-31) amide presents a favorable safety profile due to
its targeted action, comprehensive screening, and careful monitoring during treatment, it remains
essential to minimize risks and maximize clinical benefits.