Synonym |
pTH (1-38) |
Species |
Human |
Protein Accession |
P01270 |
Purity |
Greater than 95% as determined by SDS-PAGE |
Endotoxin Level |
Less than 1 EU/ug |
Biological Activity |
The ED50 for this effect is typically 3-18 ng/mL |
Expression System |
E. coli |
Fusion Tag |
None |
Predicted Molecular Mass |
4.2 kDa |
Formulation |
Lyophilized from a 0.2 μm filtered solution of 20mM PB, 150mM NaCl, pH 7.2 |
Reconstitution |
Centrifuge the vial prior to opening. Reconstitute in water to a concentration of 0.1-1.0 mg/ml.
|
Storage & Stability |
Store at -20°C. Aliquot and store at -20°C for long term. Avoid repeated freeze/thaw cycles.
|
FAQ
What is pTH (1-38) (human) and how does it work in the body?
Parathyroid hormone (pTH) is a
crucial hormone responsible for regulating calcium levels within the blood. The specific segment, pTH
(1-38) (human), refers to the amino acid sequence of the hormone that is biologically active in humans.
This segment is the necessary portion of the hormone that retains the physiological properties needed to
regulate calcium and phosphate levels effectively. The parathyroid glands, situated behind the thyroid
gland in the neck, produce this hormone in response to changes in serum calcium levels. When blood
calcium levels drop, the hormone is released into the bloodstream. pTH (1-38), upon release, acts on
three primary target areas: the bones, the kidneys, and the small intestine. In bones, pTH increases the
release of calcium by stimulating bone resorption, a process where calcium is mobilized from the bone
matrix into the bloodstream, making it available for physiological functions. In the kidneys, pTH
stimulates the reabsorption of calcium in the distal tubules, reducing the amount excreted through
urine. Additionally, it decreases the reabsorption of phosphate and increases the production of
1,25-dihydroxyvitamin D3, also known as calcitriol, an active form of vitamin D. The increase in
calcitriol levels enhances the absorption of dietary calcium in the small intestine, further
contributing to the normalization of blood calcium levels. Collectively, these mechanisms ensure that
the essential calcium level in the bloodstream is maintained, supporting various biological functions
such as bone mineralization, muscle contraction, nerve function, and blood clotting. A failure in the
proper regulation of this hormone can lead to significant health issues, including hypocalcemia or
hypercalcemia, each having various physiological implications. Treatments using synthetic versions of
pTH, particularly when parathyroid gland function is impaired, have been an area of interest for
therapeutic interventions addressing these conditions.
What conditions can be treated by pTH
(1-38) (human)?
pTH (1-38) (human) is primarily used in clinical settings to address conditions
related to abnormal calcium and phosphate metabolism. One of the main conditions treated with pTH is
hypoparathyroidism, a disorder characterized by insufficient production of the parathyroid hormone. This
insufficiency leads to low calcium and elevated phosphate levels in the blood, often resulting in muscle
cramps, tetany, fatigue, and sometimes seizures. By administering a synthetic form of pTH (1-38),
healthcare providers can mitigate these symptoms by effectively managing and restoring the calcium
levels in the bloodstream. The administration of this hormone can significantly improve patients'
quality of life by reducing the symptoms associated with calcium deficiency. Another condition where pTH
administration is considered is osteoporosis, especially in cases where traditional medications, such as
bisphosphonates, are ineffective or unsuitable. Osteoporosis is a condition marked by weakened bones and
an increased risk of fractures, often due to hormonal changes or deficiency over time. pTH (1-38), as an
anabolic agent, stimulates bone formation, increasing both the density and strength of the bone tissue.
By enhancing bone mass, the risk of fractures is considerably reduced, providing a proactive approach to
managing bone health. Furthermore, pTH analogs have been explored in situations involving bone defects
or fractures that require accelerated healing. The ability of pTH (1-38) to modulate bone remodeling and
formation positions it as a valuable tool in regenerative medicine, particularly in the context of
skeletal repair and recovery. Through its intervention, pTH (1-38) aids in the holistic improvement of
bone health and mineral balance, proving its therapeutic potential across a spectrum of mineral
metabolism disorders.
Are there any side effects associated with pTH (1-38) (human)
treatment?
The administration of pTH (1-38) (human) as a treatment for conditions such as
hypoparathyroidism or osteoporosis can be accompanied by side effects, as is the case with most
therapeutic interventions. The side effects commonly noted with pTH use can vary in severity and
frequency among individuals, depending on factors like dosage, duration of treatment, and individual
sensitivity to the hormone. Common side effects include hypercalcemia, which is an abnormally high level
of calcium in the bloodstream. This can result in symptoms such as nausea, vomiting, constipation, and
confusion. In some cases, hypercalcemia can lead to more severe complications, such as cardiac
arrhythmias or kidney stone formation, if not properly managed. Additionally, some individuals might
experience local reactions at the injection site, such as pain, redness, or swelling. Fatigue, muscle
weakness, and headaches are also reported occasionally in patients undergoing treatment. It is crucial
that healthcare providers closely monitor calcium levels in patients receiving pTH therapy to mitigate
the risk of hypercalcemia and adjust the treatment regimen accordingly. Moreover, while uncommon, some
patients might develop antibodies against the synthetic hormone, potentially reducing its efficacy over
time. In such cases, alternative therapies may need to be considered. Long-term side effects and the
potential impact on bone density need to be evaluated, especially in osteoporosis patients, to ensure
that the treatment continues to offer more benefits than risks. Despite these possible side effects, the
benefits of pTH (1-38) therapies in correcting severe calcium imbalances and improving bone health often
outweigh the risks, provided that therapy is executed with stringent clinical oversight and personalized
patient management.
How is pTH (1-38) (human) administered and what precautions should be
taken?
pTH (1-38) (human) is typically administered through subcutaneous injection, which allows
for the direct introduction of the hormone into the bloodstream. Subcutaneous administration is favored
in this context as it ensures a steady release and absorption, making it effective in managing calcium
levels consistently. Dosage and frequency depend largely on the specific condition being treated, the
severity of the disease, and the individual patient’s response to the hormone therapy. Usually,
healthcare practitioners determine a starting dose and adjust it over time based on monitoring results
and side effects, ensuring that the patient achieves optimal calcium levels while minimizing adverse
reactions. Healthcare providers must take several precautions when administering pTH (1-38) to ensure
safety and efficacy. It is imperative to assess the patient's medical history for any contraindications
or potential drug interactions, especially with medications like digitalis, which has heightened effects
due to increased calcium levels. Patients with a history of hypercalcemia or severe renal impairment
need close monitoring given the hormone’s role in calcium and phosphate metabolism. Prior to starting
treatment, baseline calcium, phosphate, and renal function tests are essential to establish an initial
reference point for safe administration. Continuous monitoring allows for timely intervention should
levels begin to fluctuate outside the normal range during treatment. It is vital for patients to receive
proper education on the self-administration technique if they are to manage injections at home,
including instructions on proper needle disposal and understanding potential side effects that require
prompt medical attention. Additionally, these individuals should be encouraged to maintain consistent
hydration and dietary calcium intake to support therapy effectiveness. Regular follow-up appointments
are necessary to re-evaluate the dosing regimen and to check for any development of side effects or
treatment resistance. Through vigilant oversight and patient education, pTH (1-38) administration can
remain a safe and highly effective treatment option.
What is the difference between pTH (1-38)
(human) and pTH (1-84) used in treatments?
Both pTH (1-38) (human) and pTH (1-84) are synthetic
forms of parathyroid hormone used in specific therapeutic contexts, yet they have distinct differences
that influence their use and efficacy. The primary difference resides in their molecular structure,
where pTH (1-38) represents the first 38 amino acids of the parathyroid hormone, while pTH (1-84)
includes the complete sequence of 84 amino acids. This structural variation impacts their mechanism of
action, receptor affinity, and biological activity over time. pTH (1-38) has been engineered to focus on
key physiological effects required for the treatment of certain conditions like osteoporosis and
hypoparathyroidism, capitalizing on its ability to regulate calcium through actions predominantly at the
receptors involved in calcium metabolism. This truncated form has sufficient biological activity to
mediate bone metabolism and calcium levels effectively, often favored for targeted short-term
therapeutic engagements. Conversely, pTH (1-84) is closer to the natural human parathyroid hormone,
offering a broader range of biological effects that mirror the hormone's role in the body more
extensively. It is often utilized in cases where a wider scope of parathyroid hormone function is
desired. Moreover, balancing these therapies requires an assessment of patient-specific needs, dosing
convenience, and potential side effect profiles. The complete sequence of pTH (1-84) can in some
instances lead to differential immune responses or longer maintenance of elevated calcium levels,
factors which may be seen as advantageous or as constraints depending on individual clinical scenarios.
Treatment outcomes may vary based on the choice between these two forms, making it crucial for
healthcare providers to consider these differences within the context of the patient's specific clinical
presentation and therapeutic goals. Ongoing studies and clinical trials continue to evaluate the
respective benefits of each treatment, informing future decisions and enhancing patient care
strategies.
What should patients discuss with their healthcare provider before starting pTH
(1-38) (human) therapy?
Before initiating pTH (1-38) (human) therapy, patients should engage in a
comprehensive discussion with their healthcare provider to ensure a thorough understanding of the
treatment, its implications, and associated precautions. First and foremost, it is crucial to discuss
the specific condition being targeted, including symptoms, diagnosis, and why pTH (1-38) is recommended
as an appropriate treatment option. This understanding helps set clear expectations regarding the
therapy's intended effects and duration. Patients should provide a complete medical history, emphasizing
any past incidences of hypercalcemia, kidney disorders, or any other bone metabolic disorders that might
influence treatment outcomes. It's also important for patients to disclose all medications they are
currently taking, including prescription drugs, over-the-counter medications, supplements, and herbal
products. This disclosure is crucial to avoid potential drug interactions that could compromise the
efficacy of the treatment or lead to adverse effects. For instance, interactions with digitalis or
calcium supplements may exacerbate certain side effects such as calcium levels. Patients should inquire
about the procedure for administering the injections, particularly if they will be self-administering
the hormone. Discussing proper injection techniques, needle disposal methods, and potential sites for
injection can enhance confidence and self-sufficiency in managing the therapy at home. Additionally,
discussing the monitoring process is essential. Understanding which tests will be required, their
frequency, and what the results indicate helps patients actively participate in their own care and
recognize the significance of adhering to medical advice and reporting any unusual symptoms they may
experience. Patients should also ask about lifestyle modifications that could complement the treatment,
such as dietary changes, exercise recommendations, and strategies for symptom management. This holistic
approach ensures that the hormone therapy aligns well with the overall care plan tailored to the
patient's unique health needs and lifestyle.