LEVEL 4 H05BA01

Δραστικές

SALMON

Φάρμακα

  • DRUGBANK - Salmon Calcitonin
  • indication:

    For the treatment of post-menopausal osteoporosis

  • pharmacology:

  • mechanism:

    Calcitonin binds to the calcitonin receptor (found primarily in osteoclasts) which then enhances the production of vitamin D producing enzymes (25-hydroxyvitamine D-24-hydroxylase), leading to greater calcium retention and enhanced bone density. Binding of calcitonin to its receptor also activates adenylyl cyclase and the phosphatidyl-inositol-calcium pathway.

  • toxicity:

    Salmon calcitonin is devoid of embryotoxic, teratogenic and mutagenic potential.

  • absorprion:

    Salmon calcitonin is rapidly absorbed and eliminated. Bioavailability following subcutaneous and intramuscular injection in humans is high and similar for the two routes of administration (71% and 66%, respectively).

  • halflife:

    50-80 minutes

  • roouteelimination:

    Studies with injectable calcitonin show increases in the excretion of filtered phosphate, calcium, and sodium by decreasing their tubular reabsorption in the kidney.

  • volumedistribution:

  • clearance: