Langbahn Team – Weltmeisterschaft

Calcitonin

CALCA
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesCALCA, CT, CGRP-I, CGRP-alpha, KC, PCT, calcitonin related polypeptide alpha, CGRP, CGRP1, CALC1
External IDsOMIM: 114130; MGI: 2151253; HomoloGene: 88401; GeneCards: CALCA; OMA:CALCA - orthologs
Orthologs
SpeciesHumanMouse
Entrez

796

12310

Ensembl

ENSG00000110680

ENSMUSG00000030669

UniProt

P06881

P70160
Q99JA0

RefSeq (mRNA)

NM_001033952
NM_001033953
NM_001741
NM_001378949
NM_001378950

NM_001033954
NM_007587
NM_001289444
NM_001305616

RefSeq (protein)

NP_001029125.1

Location (UCSC)Chr 11: 14.97 – 14.97 MbChr 7: 114.23 – 114.24 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Calcitonin is a 32 amino acid peptide hormone secreted by parafollicular cells (also known as C cells) of the thyroid (or endostyle) in humans and other chordates[5] in the ultimopharyngeal body.[6] It acts to reduce blood calcium (Ca2+), opposing the effects of parathyroid hormone (PTH).[7]

Its importance in humans has not been as well established as its importance in other animals, as its function is usually not significant in the regulation of normal calcium homeostasis.[8] It belongs to the calcitonin-like protein family.

Historically calcitonin has also been called thyrocalcitonin.[9]

Biosynthesis and regulation

Calcitonin is formed by the proteolytic cleavage of a larger prepropeptide, which is the product of the CALC1 gene (CALCA). It is functionally an antagonist with PTH and Vitamin D3. The CALC1 gene belongs to a superfamily of related protein hormone precursors including islet amyloid precursor protein, calcitonin gene-related peptide, and the precursor of adrenomedullin.

Secretion of calcitonin is stimulated by:

Function

Main article: Calcium metabolism

The hormone participates in calcium (Ca2+) metabolism. In many ways, calcitonin counteracts parathyroid hormone (PTH) and vitamin D.

More specifically, calcitonin lowers blood Ca2+ levels in two ways:

High concentrations of calcitonin may be able to increase urinary excretion of calcium and phosphate via the renal tubules.[15] leading to marked hypocalcemia. However, this is a minor effect with no physiological significance in humans. It is also a short-lived effect because the kidneys become resistant to calcitonin, as demonstrated by the kidney's unaffected excretion of calcium in patients with thyroid tumors that secrete excessive calcitonin.[16]

In its skeleton-preserving actions, calcitonin protects against calcium loss from the skeleton during periods of calcium mobilization, such as pregnancy and, especially, lactation. The protective mechanisms include the direct inhibition of bone resorption and the indirect effect through the inhibition of the release of prolactin from the pituitary gland. The reason provided is that prolactin induces the release of PTH related peptide which enhances bone resorption, but is still under investigation.[17][18][19]

Other effects are in preventing postprandial hypercalcemia resulting from absorption of Ca2+. Also, calcitonin inhibits food intake in rats and monkeys, and may have CNS action involving the regulation of feeding and appetite.

Calcitonin lowers blood calcium and phosphorus mainly through its inhibition of osteoclasts. Osteoblasts do not have calcitonin receptors and are therefore not directly affected by calcitonin levels. However, since bone resorption and bone formation are coupled processes, eventually calcitonin's inhibition of osteoclastic activity leads to increased osteoblastic activity (as an indirect effect).[16]

Receptor

Structure of human calcitonin recptor-Gs complex. The transmembrane calcitonin receptor (blue) is bound to human calcitonin (red) and the Gs complex (yellow). PDB: 7TYO​

The calcitonin receptor is a G protein-coupled receptor localized to osteoclasts[20] as well kidney and brain cells. It is coupled to a Gsα subunit, thus stimulating cAMP production by adenylate cyclase in target cells. It may also affect the ovaries in women and the testes in men.[citation needed]

Discovery

Calcitonin was first purified in 1962 by Douglas Harold Copp and B. Cheney at the University of British Columbia, Canada.[21] It was initially thought to be secreted by the parathyroid gland but was shown by Iain Macintyre and his team at the Royal Postgraduate Medical School, London, to be secreted by parafollicular cells of the thyroid gland.[22] Dr. Copp named the discovered hormone calcitonin because of its role in 'maintaining normal calcium tone'.[21]

Clinical significance

Calcitonin assay is used in identifying patients with nodular thyroid diseases. It is helpful in making an early diagnosis of medullary carcinoma of thyroid. A malignancy of the parafollicular cells, i.e. medullary thyroid cancer (MTC), typically produces an elevated serum calcitonin level. Prognosis of MTC depends on early detection and treatment.

Calcitonin also has significantly impacted molecular biology, as the gene encoding calcitonin was the first gene discovered in mammalian cells to be alternatively spliced, now known to be a ubiquitous mechanism in eukaryotes.[23][24]

Pharmacology

Calcitonin has clinically been used for metabolic bone disorders for more than 50 years.[25] Salmon calcitonin is used for the treatment of:

It has been investigated as a possible non-operative treatment for spinal stenosis.[31]

The following information is from the UK Electronic Medicines Compendium[32]

General characteristics of the active substance

Salmon calcitonin is rapidly absorbed and eliminated. Peak plasma concentrations are attained within the first hour of administration.

Animal studies have shown that calcitonin is primarily metabolised via proteolysis in the kidney following parenteral administration. The metabolites lack the specific biological activity of calcitonin. Bioavailability following subcutaneous and intramuscular injection in humans is high and similar for the two routes of administration (71% and 66%, respectively).

Calcitonin has short absorption and elimination half-lives of 10–15 minutes and 50–80 minutes, respectively. Salmon calcitonin is primarily and almost exclusively degraded in the kidneys, forming pharmacologically inactive fragments of the molecule. Therefore, the metabolic clearance is much lower in patients with end-stage kidney failure than in healthy subjects. However, the clinical relevance of this finding is not known. Plasma protein binding is 30% to 40%.

Characteristics in patients

There is a relationship between the subcutaneous dose of calcitonin and peak plasma concentrations. Following parenteral administration of 100 IU calcitonin, peak plasma concentration lies between about 200 and 400 pg/ml. Higher blood levels may be associated with increased incidence of nausea, vomiting, and secretory diarrhea.

Preclinical safety data

Conventional long-term toxicity, reproduction, mutagenicity, and carcinogenicity studies have been performed in laboratory animals. Salmon calcitonin is devoid of embryotoxic, teratogenic, and mutagenic potential.

An increased incidence of pituitary adenomas has been reported in rats given synthetic salmon calcitonin for 1 year. This is considered a species-specific effect and of no clinical relevance.[33] Salmon calcitonin does not cross the placental barrier.

In lactating animals given calcitonin, suppression of milk production has been observed. Calcitonin is secreted into the milk.

Pharmaceutical manufacture

Calcitonin was extracted from the ultimobranchial glands (thyroid-like glands) of fish, particularly salmon. Salmon calcitonin resembles human calcitonin, but is more active. At present, it is produced either by recombinant DNA technology or by chemical peptide synthesis. The pharmacological properties of the synthetic and recombinant peptides have been demonstrated to be qualitatively and quantitatively equivalent.[32]

Uses of calcitonin

Treatments

Calcitonin affecting the spine.

Calcitonin can be used therapeutically for the treatment of hypercalcemia or osteoporosis.[34] In a recent clinical study, subcutaneous injections of calcitonin have reduced the incidence of fractures and reduced the decrease in bone mass in women with type 2 diabetes complicated with osteoporosis.[35]

Subcutaneous injections of calcitonin in patients with mania resulted in significant decreases in irritability, euphoria and hyperactivity and hence calcitonin holds promise for treating bipolar disorder.[36] However no further work on this potential application of calcitonin has been reported.

Diagnostics

It may be used diagnostically as a tumor marker for medullary thyroid cancer, in which high calcitonin levels may be present and elevated levels after surgery may indicate recurrence. It may even be used on biopsy samples from suspicious lesions (e.g., lymph nodes that are swollen) to establish whether they are metastases of the original cancer.

Cutoffs for calcitonin to distinguish cases with medullary thyroid cancer have been suggested to be as follows, with a higher value increasing the suspicion of medullary thyroid cancer:[37]

  • females: 5 ng/L or pg/mL
  • males: 12 ng/L or pg/mL
  • children under 6 months of age: 40 ng/L or pg/mL
  • children between 6 months and 3 years of age: 15 ng/L or pg/mL

When over 3 years of age, adult cutoffs may be used

A Cochrane systematic review assessed the diagnostic accuracy of basal and stimulated calcitonin for Medullary Thyroid cancer.[38] Although both basal and combined basal and stimulated calcitonin testing presented high accuracy (sensitivity: between 82% and 100%; specificity: between 97.2% and 100%), these results had a high risk of bias due to design flaws of included studies.[38] Overall, the value of routine testing of calcitonin for diagnosis and prognosis of Medullary Thyroid Cancer remains uncertain and questionable.[38]

Increased levels of calcitonin have also been reported for various other conditions. They include: C-cell hyperplasia, nonthyroidal oat cell carcinoma, nonthyroidal carcinoma and other nonthyroidal malignancies, acute kidney injury and chronic kidney failure, hypercalcemia, hypergastrinemia, and other gastrointestinal disorders, and pulmonary disease.[39]

Structure

Calcitonin is a polypeptide hormone of 32 amino acids, with a molecular weight of 3454.93 daltons. Its structure comprises a single alpha helix.[40] Alternative splicing of the gene coding for calcitonin produces a distantly related peptide of 37 amino acids, called calcitonin gene-related peptide (CGRP), beta type.[41]

The following are the amino acid sequences of salmon and human calcitonin:[citation needed][42]

  • salmon:

Cys-Ser-Asn-Leu-Ser-Thr-Cys-Val-Leu-Gly-Lys-Leu-Ser-Gln-Glu-Leu-His-Lys-Leu-Gln-Thr-Tyr-Pro-Arg-Thr-Asn-Thr-Gly-Ser-Gly-Thr-Pro

  • human:

Cys-Gly-Asn-Leu-Ser-Thr-Cys-Met-Leu-Gly-Thr-Tyr-Thr-Gln-Asp-Phe-Asn-Lys-Phe-His-Thr-Phe-Pro-Gln-Thr-Ala-Ile-Gly-Val-Gly-Ala-Pro

Compared to salmon calcitonin, human calcitonin differs at 16 residues.

Research

In addition to the injectable and nasal spray dosage forms of the salmon calcitonin, noninvasive oral formulations of the peptide are currently under clinical development. The short-half-life of this peptide in serum triggered several attempts to enhance plasma concentrations. The peptide is complexed with a macromolecule that acts as an absorption enhancer through the transcellular pathway and, additionally, protects the peptide from the harsh pH and enzymatic conditions of the GI tract. This complexation is weak, noncovalent and reversible and the drug remains chemically unmodified. After passage through the intestine, the delivery agent dissociates from the peptide. One of the extensively studied oral formulations is the disodium salts of 5-CNAC oral calcitonin. This novel oral platform in a number of clinical trials at different phases has demonstrated promising enhanced pharmacokinetic profile, high bioavailability, well-established safety and comparable efficacy to that of nasal calcitonin especially for treatment of postmenopausal bone loss.[25]

See also

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000110680 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030669 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Sekiguchi T, Kuwasako K, Ogasawara M, Takahashi H, Matsubara S, Osugi T, et al. (January 2016). "Evidence for Conservation of the Calcitonin Superfamily and Activity-regulating Mechanisms in the Basal Chordate Branchiostoma floridae: Insights Into the Molecular and Functional Evolution in Chordates". The Journal of Biological Chemistry. 291 (5): 2345–2356. doi:10.1074/jbc.M115.664003. PMC 4732217. PMID 26644465.
  6. ^ Costoff A. "Sect. 5, Ch. 6: Anatomy, Structure, and Synthesis of Calcitonin (CT)". Endocrinology: hormonal control of calcium and phosphate. Medical College of Georgia. Archived from the original on September 5, 2008. Retrieved 2008-08-07.
  7. ^ Boron WF, Boulpaep EL (2004). "Endocrine system chapter". Medical Physiology: A Cellular And Molecular Approach. Elsevier/Saunders. ISBN 1416023283.
  8. ^ Costoff A. "Sect. 5, Ch. 6: Biological Actions of CT". Medical College of Georgia. Archived from the original on July 5, 2008. Retrieved 2008-08-07.
  9. ^ Felsenfeld AJ, Levine BS (April 2015). "Calcitonin, the forgotten hormone: does it deserve to be forgotten?". Clinical Kidney Journal. 8 (2): 180–187. doi:10.1093/ckj/sfv011. PMC 4370311. PMID 25815174.
  10. ^ Costanzo LS (2007). BRS Physiology. Lippincott, Williams, & Wilkins. pp. 263. ISBN 978-0-7817-7311-9.
  11. ^ Erdogan MF, Gursoy A, Kulaksizoglu M (October 2006). "Long-term effects of elevated gastrin levels on calcitonin secretion". J. Endocrinol. Invest. 29 (9): 771–5. doi:10.1007/BF03347369. PMID 17114906. S2CID 41798141.
  12. ^ Costoff A. "Sect. 5, Ch. 6: Effects of CT on Bone". Medical College of Georgia. Archived from the original on June 22, 2008. Retrieved 2008-08-07.
  13. ^ Potts J, Jüppner H (2008). "Chapter 353. Disorders of the Parathyroid Gland and Calcium Homeostasis". In Longo DL, Kasper DL, Jameson JL, Fauci AS, Hauser SL, Loscalzo J (eds.). Harrison's Principles of Internal Medicine (18th ed.). McGraw-Hill. Archived from the original on 2017-05-08. Retrieved 2017-05-29.
  14. ^ Rhoades R (2009). Medical Physiology: Principles for Clinical Medicine. Philadelphia: Lippincott Williams & Wilkins. ISBN 978-0781768528.[page needed]
  15. ^ Carney SL (1997). "Calcitonin and human renal calcium and electrolyte transport". Mineral and Electrolyte Metabolism. 23 (1): 43–47. PMID 9058369.
  16. ^ a b Goodman HM (2009). Basic Medical Endocrinology (Fourth ed.). Elsevier. ISBN 978-0123739759.[page needed]
  17. ^ Horwitz MJ, Tedesco MB, Sereika SM, Syed MA, Garcia-Ocaña A, Bisello A, et al. (October 2005). "Continuous PTH and PTHrP infusion causes suppression of bone formation and discordant effects on 1,25(OH)2 vitamin D". J. Bone Miner. Res. 20 (10): 1792–1803. doi:10.1359/JBMR.050602. PMID 16160737. S2CID 25594820.
  18. ^ Davey RA, Turner AG, McManus JF, Chiu WS, Tjahyono F, Moore AJ, et al. (August 2008). "Calcitonin receptor plays a physiological role to protect against hypercalcemia in mice". J. Bone Miner. Res. 23 (8): 1182–1193. doi:10.1359/jbmr.080310. PMC 2680171. PMID 18627265.
  19. ^ Woodrow JP, Sharpe CJ, Fudge NJ, Hoff AO, Gagel RF, Kovacs CS (September 2006). "Calcitonin plays a critical role in regulating skeletal mineral metabolism during lactation". Endocrinology. 147 (9): 4010–4021. doi:10.1210/en.2005-1616. PMID 16675524.
  20. ^ Nicholson GC, Moseley JM, Sexton PM, Mendelsohn FA, Martin TJ (August 1986). "Abundant calcitonin receptors in isolated rat osteoclasts. Biochemical and autoradiographic characterization". J. Clin. Invest. 78 (2): 355–360. doi:10.1172/JCI112584. PMC 423551. PMID 3016026.
  21. ^ a b Copp DH, Cheney B (January 1962). "Calcitonin-a hormone from the parathyroid which lowers the calcium-level of the blood". Nature. 193 (4813): 381–2. Bibcode:1962Natur.193..381C. doi:10.1038/193381a0. PMID 13881213. S2CID 4292938.
  22. ^ Foster GV, Baghdiantz A, Kumar MA, Slack E, Soliman HA, Macintyre I (June 1964). "Thyroid origin of calcitonin". Nature. 202 (4939): 1303–5. Bibcode:1964Natur.202.1303F. doi:10.1038/2021303a0. PMID 14210962. S2CID 2443410.
  23. ^ Rosenfeld MG, Amara SG, Roos BA, Ong ES, Evans RM (March 1981). "Altered expression of the calcitonin gene associated with RNA polymorphism". Nature. 290 (5801): 63–65. Bibcode:1981Natur.290...63R. doi:10.1038/290063a0. PMID 7207587. S2CID 4318349.
  24. ^ Rosenfeld MG, Lin CR, Amara SG, Stolarsky L, Roos BA, Ong ES, et al. (March 1982). "Calcitonin mRNA polymorphism: peptide switching associated with alternative RNA splicing events". Proceedings of the National Academy of Sciences of the United States of America. 79 (6): 1717–1721. Bibcode:1982PNAS...79.1717R. doi:10.1073/pnas.79.6.1717. PMC 346051. PMID 6952224.
  25. ^ a b das Neves J, Sarmento B (2014). "Eligen® Technology for Oral Delivery of Proteins and Peptides". Mucosal Delivery of Biopharmaceuticals. Boston: Springer US. pp. 407–422. doi:10.1007/978-1-4614-9524-6_18. ISBN 978-1461495246.
  26. ^ "Handout on Health: Osteoporosis". NIAMS. August 2014. Archived from the original on 18 May 2015. Retrieved 16 May 2015.
  27. ^ "Hypercalcemia". The Lecturio Medical Concept Library. Retrieved 1 October 2021.
  28. ^ MedlinePlus Overview bonecancer
  29. ^ "Paget's Disease of Bone". The Lecturio Medical Concept Library. Retrieved 1 October 2021.
  30. ^ Wall GC, Heyneman CA (April 1999). "Calcitonin in phantom limb pain". The Annals of Pharmacotherapy. 33 (4): 499–501. doi:10.1345/aph.18204. PMID 10332543. S2CID 30651328.
  31. ^ Tran DQ, Duong S, Finlayson RJ (July 2010). "Lumbar spinal stenosis: a brief review of the nonsurgical management". Can J Anaesth. 57 (7): 694–703. doi:10.1007/s12630-010-9315-3. PMID 20428988.
  32. ^ a b "Electronic Medicines Compendium". Archived from the original on 2005-11-08. Retrieved 2008-08-07.
  33. ^ "Injectable Salmon Calcitonin" (PDF). Archived from the original (PDF) on 2018-06-18. Retrieved 2017-02-07.
  34. ^ Inzerillo AM, Zaidi M, Huang CL (2004). "Calcitonin: physiological actions and clinical applications". Journal of Pediatric Endocrinology & Metabolism. 17 (7): 931–940. doi:10.1007/s00198-015-3149-3. PMID 15301040. S2CID 23551343.
  35. ^ Dexue L, Yueyue Z (November 2014). "Salmon calcitonin in the treatment of elderly women with type 2 diabetes complicated with osteoporosis". Pak J Pharm Sci. 27 (6 Suppl): 2079–2081. PMID 25410076.
  36. ^ Vik A, Yatham LN (March 1998). "Calcitonin and bipolar disorder: a hypothesis revisited". Journal of Psychiatry & Neuroscience. 23 (2): 109–117. PMC 1188909. PMID 9549251.
  37. ^ Basuyau JP, Mallet E, Leroy M, Brunelle P (October 2004). "Reference intervals for serum calcitonin in men, women, and children". Clin. Chem. 50 (10): 1828–1830. doi:10.1373/clinchem.2003.026963. PMID 15388660.
  38. ^ a b c Verbeek HH, de Groot JW, Sluiter WJ, Muller Kobold AC, van den Heuvel ER, Plukker JT, et al. (Cochrane Metabolic and Endocrine Disorders Group) (March 2020). "Calcitonin testing for detection of medullary thyroid cancer in people with thyroid nodules". The Cochrane Database of Systematic Reviews. 2020 (3): CD010159. doi:10.1002/14651858.CD010159.pub2. PMC 7075519. PMID 32176812.
  39. ^ Burtis CA, Ashwood ER, Bruns DE (2012). Tietz Textbook of Clinical Chemistry and Molecular Diagnostics (5th ed.). Elsevier Saunders. p. 1774. ISBN 978-1-4160-6164-9.
  40. ^ Andreotti G, Méndez BL, Amodeo P, Morelli MA, Nakamuta H, Motta A (August 2006). "Structural determinants of salmon calcitonin bioactivity: the role of the Leu-based amphipathic alpha-helix". J. Biol. Chem. 281 (34): 24193–241203. doi:10.1074/jbc.M603528200. PMID 16766525.
  41. ^ "calcitonin domain annotation". SMART (a Simple Modular Architecture Research Tool). embl-heidelberg.de. Retrieved 2009-02-22.
  42. ^ "Salmon calicitonin". prospecbio.

Further reading

Quelle: https://en.wikipedia.org/wiki/CALCA