A 30-day preclinical safety evaluation study of recombinant human follicle-stimulating hormone in female rhesus monkeys

Int J Toxicol. 2011 Mar;30(2):153-61. doi: 10.1177/1091581810390823. Epub 2011 Mar 14.

Abstract

The objective of this study was to identify potential target organs for toxicity of recombinant human follicle stimulating hormone (r-hFSH) in female rhesus monkeys and to establish a no observed adverse effect level (NOAEL). In all, 24 female rhesus monkeys (Chinese origin, weighing 3.4-5.2 kg, approximately 5 years of age) received repeated subcutaneous (sc) r-hFSH at doses of 10, 60, and 300 IU/kg per d or vehicle once daily for 30 days followed by a 15-day recovery period. Endometrial hyperplasia and dermal edema in the external genitals were found in some animals at 300 IU/kg per d. Pharmacologic-related multiple cystic follicles were found in all r-hFSH-treated groups. A weak, anti-FSH antibody response was detected at the end of treatment in animals administered 60 and 300 IU/kg per d. These results indicate that the primary effects of r-hFSH in female rhesus monkeys were related to its pharmacological activity on the reproductive system. The NOAEL was considered to be 60 IU/kg per d.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies / blood
  • Dose-Response Relationship, Drug
  • Drug Evaluation, Preclinical
  • Endometrial Hyperplasia / pathology
  • Female
  • Follicle Stimulating Hormone, Human / administration & dosage*
  • Follicle Stimulating Hormone, Human / toxicity*
  • Gonadal Steroid Hormones / blood
  • Injections, Subcutaneous
  • Macaca mulatta
  • No-Observed-Adverse-Effect Level
  • Ovarian Follicle / drug effects*
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / toxicity
  • Toxicity Tests

Substances

  • Antibodies
  • Follicle Stimulating Hormone, Human
  • Gonadal Steroid Hormones
  • Recombinant Proteins