Development and characterization of a long‐acting recombinant hFSH agonist
Klein
Joshua U.
author
Columbia University. Obstetrics and Gynecology
Lobel
Leslie I.
author
Columbia University. Obstetrics and Gynecology
Pollack
Susan V.
author
Columbia University. Obstetrics and Gynecology
Lustbader
Brandie
author
Ogden
Robert T.
author
Columbia University. Biostatistics
Sauer
Mark V.
author
Columbia University. Obstetrics and Gynecology
Lustbader
Joyce W.
author
Columbia University. Obstetrics and Gynecology
Columbia University. Obstetrics and Gynecology
originator
text
Articles
2003
English
Background: Fusion of the carboxyterminal peptide (CTP) of hCG to FSH results in a follitropin agonist with an extended half-life, presumably due to the four O-oligosaccharides on the CTP. Alternatively, an rhFSH analogue containing additional N-linked carbohydrate is described in this report. Methods: A DNA sequence containing two N-oligosaccharide signal sequences was ligated into a vector containing hFSHβ- and α-subunit encoding cDNA, and expressed in CHO-K1 cells. In-vitro bioactivity of the single-chain hormone was assessed in CHO cells expressing the hFSH receptor. Pharmacokinetic values were derived from serial serum assays of the analogue in immature female rats following a single i.v. injection. In-vivo bioactivity was assessed by measuring ovarian weight gain 3 days post-injection. Results: rhFSH-N2 and native rhFSH induced comparable levels of cAMP in vitro. t1/2 for native rhFSH, rhFSH-CTP and rhFSH-N2 were 3.7, 7.1 and 7.3 h respectively. Rats receiving rhFSH-N2 had a mean ± SD ovarian weight 3 days post-i.v. injection (22 ± 3.6 mg) significantly greater than rats receiving rhFSH and saline (16.7 ± 1.5 and 15.3 ± 0.47 mg respectively, P < 0.05). Conclusions: rhFSH-N2 has prolonged half-life and increased bioactivity compared with native rhFSH. This rhFSH agonist, and other analogues containing additional N-oligosaccharides may have important clinical applications.
Obstetrics and gynecology
Pharmacology
Human Reproduction
18
1
50
56
2003-01
http://dx.doi.org/10.1093/humrep/deg024
http://hdl.handle.net/10022/AC:P:14414
NNC
NNC
2012-08-16 15:12:37 -0400
2012-08-16 15:44:25 -0400
8434
eng