Taiy Chemical
Calcitonin (chicken)
Synonym CALCA, CALC1, CGRP, CGRP-I, CGRP1, DKFZp781I14186, MGC75148
Species Chicken
Protein Accession P01259
Purity > 95%
Endotoxin Level < 1 EU/ug
Biological Activity Not determined
Expression System E. coli
Fusion Tag None
Predicted Molecular Mass 13.1 kDa
Formulation Lyophilized from a 0.2 μm filtered solution in Acetonitrile and TFA
Reconstitution Centrifuge the vial prior to opening. Reconstitute in 20 mM Acetic Acid to a concentration of 0.1-1.0 mg/ml.
Storage & Stability Store at -20°C. For long term storage, store at -80°C. Once reconstituted, the protein should be stored at -20°C.
FAQ
What is Calcitonin (chicken) and how does it work within the body?

Calcitonin (chicken) is a form of the hormone calcitonin, which is naturally produced in the thyroid gland of humans and other mammals. Its primary role in the body is to help regulate calcium levels by inhibiting bone resorption and promoting the incorporation of calcium into the bone matrix. In essence, calcitonin lowers calcium levels in the blood when they become too high. The chicken version of calcitonin has shown effectiveness in similar roles and is often used in research or therapeutic contexts. It acts by binding to specific receptors on osteoclasts, the cells responsible for bone resorption. Osteoclasts break down bone tissue, releasing calcium into the bloodstream, but when calcitonin binds to its receptor on these cells, their bone-resorbing activity is diminished. This hormonal binding cascade is essential in the treatment of diseases where bone preservation and regulated calcium levels are critical, such as osteoporosis, Paget’s disease, and other bone-related metabolic disorders. This kind of calcitonin exerts its effects by mimicking the action of human calcitonin, even though there might be small differences in the sequence of amino acids, the fundamental building blocks of proteins. These differences do not alter the hormone's effectiveness significantly but offer an alternative source for treatment. Calcitonin (chicken) contributes to bone metabolism by slowing abnormal bone loss while promoting the retention of bone density and strength. In therapeutic settings, it can be administered via injection or nasal spray, allowing the hormone to act systemically. While the mechanism of action is well-understood in terms of receptor binding and inhibiting osteoclast function, ongoing research continues to explore the broader implications of its use, including potential benefits beyond calcium regulation, such as effects on pain modulation or neuroprotection. Each application aims to leverage its bone health benefits without eliciting significant side effects, making it a valuable consideration in patients with specific endocrine or bone density disorders.

How is Calcitonin (chicken) typically used in medical treatments?

Calcitonin (chicken) is primarily used in medical treatments that focus on conditions involving bone density loss and calcium metabolism anomalies, such as osteoporosis, Paget's disease, and hypercalcemia. Considering osteoporosis, calcitonin (chicken) serves as a treatment option for osteoporosis in postmenopausal women primarily to decrease the rate of bone turnover and reduce the likelihood of fractures. It acts by inhibiting osteoclast activity, which is pivotal in bone resorption processes. This suppression helps preserve bone density and may help stabilize the skeletal mass. Therapy involving calcitonin is often tailored over a prolonged period to observe significant improvements in bone mineral density and overall structural integrity. Paget's disease, a condition characterized by disordered bone remodeling, is another situation where calcitonin (chicken) can be prescribed. For Paget's disease, the goal of calcitonin therapy is to regulate the excessive breakdown and formation of bone that typifies this disorder. By doing so, it helps in relieving bone pain and reducing the risk of complications that arise due to excessively brittle and malformed bones. In cases of chronic hypercalcemia—where calcium levels in the blood are abnormally elevated and can lead to potential complications—the use of calcitonin (chicken) serves as a counteracting mechanism to lower calcium levels by reducing bone resorption. This can be crucial when addressing conditions wherein there is excessive release of calcium from the bone. Administering calcitonin (chicken) may be done via subcutaneous injection or intranasally, depending on the condition's requirements and patient adherence to treatment methods. Buffering agents or carriers often accompany the intranasal form to enhance absorption and efficacy. The choice between injection and nasal spray will also be influenced by patient convenience and the clinical judgment regarding the severity of the condition being treated. As an adjunctive therapy, it may be recommended along with other osteoporosis-targeting medications such as bisphosphonates, allowing for synergistic effects in calcium and bone metabolism regulation. While efficacious, the treatment must be continuously assessed for any adverse reactions or diminished efficacy over time, necessitating routine clinical evaluations by healthcare providers.

What are the potential benefits of using Calcitonin (chicken) for osteoporosis patients?

The potential benefits of using Calcitonin (chicken) for osteoporosis patients are substantial, primarily focusing on the preservation of bone mass and reduction of fracture risk. Osteoporosis is marked by decreased bone density and increased fragility, leading to a higher risk of fractures, particularly in the hip, spine, and wrist. Calcitonin (chicken) serves as an effective anti-resorptive agent, slowing down the rate at which bone cells break down and preserving the existing bone mass. This factor is beneficial in reducing the risk of fractures in individuals who may already have experienced bone loss over time, such as postmenopausal women. By acting to inhibit osteoclast activity, calcitonin helps to maintain bone remodeling balance, crucial for individuals with heightened bone resorption rates. Maintaining skeletal structure with a therapeutically active agent like calcitonin could lead to a reduced incidence of fractures, which are often debilitating and costly to treat. For osteoporosis patients, calcitonin (chicken) has an additional benefit in potentially reducing bone pain, providing symptomatic relief, particularly to those who suffer from acute pain due to vertebral and spinal fractures. This analgesic effect is an appealing factor in restoring a degree of functional mobility and improving the quality of life for those afflicted by the stabbing and persistent nature of osteoporosis-related pain. The nasal spray formulation of calcitonin makes it a more accessible and less invasive option for such patients, particularly beneficial for elderly patients who may have difficulty with injections or have varying levels of mobility. Despite being less potent than other medication classes like bisphosphonates, calcitonin complements broader treatment regimens, offering osteoporosis patients a less aggressive drug regimen that is well-tolerated, with a relatively mild side-effect profile. As an adjunct to other therapeutic efforts such as diet modification and augmented physical activity, calcitonin (chicken) could play a significant role in multi-pronged approaches to bone health management. It potentially aids in maintaining vital components of bone architecture and provides a viable treatment pathway when some alternatives may not be suitable, enhancing therapeutic diversity and patient-specific care opportunities.

How does Calcitonin (chicken) compare to other treatments for Paget's disease?

When assessing how Calcitonin (chicken) compares to other treatments for Paget's disease, it is insightful to consider its mechanism of action, efficacy, route of administration, side effect profile, and suitability for specific patient populations. Calcitonin (chicken) is a viable option in managing Paget's disease, working primarily through its ability to modulate osteoclast activity, thereby reducing bone turnover rates. Compared to bisphosphonates like alendronate and risedronate, which are typically considered first-line treatments due to their potency and long-term effectiveness in reducing disease activity, calcitonin may have a slightly milder effect on bone resorption. Bisphosphonates bind to the bone matrix and act more persistently, leading to prolonged suppression of osteoclastic activity, which contributes to their robust capability in normalizing bone turnover. Calcitonin may be preferred in patients who are intolerant to bisphosphonates or have contraindications due to pre-existing conditions, such as renal impairments that limit bisphosphonate use. The protein nature of calcitonin means it is usually delivered via nasal spray or injection, contrasting with the primarily oral administration of bisphosphonates. This administration aspect can be both an advantage and disadvantage. While injections ensure precise dosage control and nasal formulations often enhance user convenience, some patients may find it less desirable if consistent daily or weekly dosing rhythms are challenging to maintain. From a side-effect profile perspective, calcitonin is often well-tolerated and associated with fewer gastrointestinal issues compared to bisphosphonates, but it could induce symptoms such as nasal irritation (for nasal forms) or skin reactions (at injection sites). In some evaluations, there may be a notable difference in the reduction of pain associated with bone disorders when using calcitonin, which may appeal to patients experiencing acute discomfort from the disease. However, due to potential antibody development over time, which can neutralize the hormone's efficacy, calcitonin may lose effectiveness with long-term use, thus making it more suitable for intermittent or initial therapy forms rather than sustained long-duration treatment. Clinical evaluations and patient-specific factors often ultimately guide decisions, where the trade-offs between bone turnover control, side effects, and patient lifestyle preferences lead to an optimized therapeutic choice.

What are the side effects associated with Calcitonin (chicken) therapy?

Calcitonin (chicken) therapy, while efficacious for certain conditions like osteoporosis and Paget’s disease, does come with a spectrum of potential side effects that patients and healthcare providers need to consider. The side-effect profile introduces various mild to moderate adverse effects, largely contingent on the administration form, whether it is injection or nasal spray. For nasal administration, the most common side effects include nasal irritation, such as sneezing, runny nose, and nasal congestion. Some patients might experience nosebleeds, crusting, or ulceration over prolonged use. It is thus generally recommended for users to be vigilant about nasal health and consult healthcare providers if symptoms persist or worsen. Patients with a history of significant nasal or sinus issues might want to discuss alternative forms of administration with their healthcare provider. As for the injectable form, users may experience localized reactions at the injection site, including skin redness, swelling, or discomfort, evolving occasionally into flushing and warmth perceptions soon after administration. This response is typically related to natural inflammation mechanisms at the local administration level and can often be self-limiting, though they might sometimes affect the continuation of using injections if severe. Besides localized symptoms, there are systemic considerations, including nausea, headaches, dizziness, and, at times, cases of abdominal pain. These symptoms often appear transient and mild but are worth monitoring, especially when any new symptoms emerge post-therapy initiation. Rarely, serious allergic reactions can surface, with clinical manifestations like significant rash, itching/swelling (particularly of the face/tongue/throat), and breathing difficulties. Such reactions would necessitate immediate medical attention and cessation of therapy. Long-term calcitonin use could potentially spark an anti-calcitonin antibody response, which diminishes therapy's efficacy, meaning continuous evaluation of treatment outcomes is advised. Importantly, specific population segments, such as those with severe renal impairment, might experience exacerbated side effects, necessitating dose adjustments or therapy modifications. Depending on predisposed sensitivities and existing health conditions, healthcare providers will weigh therapeutic benefits against these adverse effect potentials, making any necessary adjustments to assure patient health and treatment alignment. The healthcare team will often advocate for an integrative approach of consistent monitoring and open communication with patients, thus ensuring that any addressed calcitonin-related concerns fit holistically within the individualized treatment landscape.
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