McMahon, A., et al. “Hexachlorobenzene Toxicity in the Monkey Primordial Germ-Cell Without Induced Porphyria”. Reproductive Toxicology, vol. 7, no. 1, 1993, pp. 41-47, https://doi.org/10.1016/0890-6238(93)90008-u.

Genre

  • Journal Article
Contributors
Author: McMahon, A.
Author: Bartlett, S.
Author: Singh, A.
Author: Franklin, C.
Author: Villeneuve, D.
Author: Valli, V. E.
Author: Jarrell, J. F.
Date Issued
1993
Abstract

Hexachlorobenzene is a persistent chlorinated organic chemical that has been detected in many tissues from a variety of species including human ovary and human ovarian follicular fluid. When administered in high dosage to nonhuman primates, hexachlorobenzene causes destruction of ovarian primordial germ cells in association with systemic toxicity. The purpose of these experiments was to assess relative ovarian germ cell sensitivity at much lower dosages of hexachlorobenzene that do not produce systemic effects and additionally to evaluate oocyte function by means of the response to superovulation, fertilization, and embryo cleavage during a cycle of in vitro fertilization in the cynomolgus monkey. Hexachlorobenzene in dosages of 0.1, 1.0, and 10.0 mg/kg/day was administered orally by gelatin capsule for 90 days. There was a dose-dependent accumulation of HCB in serum and other tissues without any change in the serum estradiol response to human menopausal gonadotropin, oocyte recovery, oocyte maturation, oocyte fertilization in vitro, and early embryo cleavage rate. There was a dose-related toxic effect observed in primordial germ cells at the lowest dose despite no evidence of systemic or hepatic effects. As there were no changes in the urinary prophyrin excretion, the mechanism of hexachlorobenzene ovotoxicity may be distinct from hexachlorobenzene-induced cytochrome P450-dependent inhibition of uroporphobilinogen decarboxylase in the liver, although such intraovarian metabolism cannot be excluded.

Note

HLTH PROTECT BRANCH,ENVIRONM HLTH DIRECTORATE,BUR CHEM HAZARDS,DIV ENVIRONM & OCCUPAT TOXICOL,OTTAWA,ON,CANADA. OFF DEPUTY MINIST HLTH & WELF,OTTAWA,ON,CANADA. UNIV PRINCE EDWARD ISL,ATLANTIC VET COLL,DEPT ANAT & PHYSIOL,CHARLOTTETOWN C1A 4P3,PE(TRUNCATED)

OXFORD; THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD, ENGLAND OX5 1GB

PERGAMON-ELSEVIER SCIENCE LTD

PT: J; CR: BABINEAU KA, 1991, J SUBMICR CYTOL PATH, V23, P457 BALMACEDA JP, 1984, FERTIL STERIL, V42, P791 BAVISTER BD, 1977, BIOL REPROD, V16, P228 BAVISTER BD, 1983, BIOL REPROD, V28, P983 BERTRAM HP, 1985, HEXACHLOROBENZENE, P173 BUMP EA, 1990, PHARMACOL THERAPEUT, V47, P117 COURTNEY KD, 1977, ENVIRON RES, V20, P255 DEBETS FMH, 1980, TOXICOLOGY, V15, P181 DOBSON RL, 1983, AM J IND MED, V4, P175 DOGRAMACI I, 1962, TURKISH J PEDIATR, V4, P129 ELDER GH, 1982, BIOCHEM BIOPH RES CO, V109, P113 GILBERTSON M, 1972, B ENVIRON CONTAM TOX, V7, P371 IATROPOULOS MJ, 1976, TOXICOL APPL PHARM, V37, P433 KNAUF V, 1979, B ENVIRON CONTAM TOX, V21, P243 NIJIUS H, 1986, IARC SCI PUBL, P133 PARKE DV, 1960, BIOCHEM J, V74, P5 PESSAYRE D, 1981, BIOCHEM PHARMACOL, V30, P559 PHELPS DK, 1986, IARC SCI PUBL, P121 RIZZARDINI M, 1988, J BIOCHEM TOXICOL, V3, P33 SCHWARTZ S, 1952, J BIOL CHEM, V194, P563 SHIROMIZU K, 1985, TERATOGEN CARCIN MUT, V5, P463 SIMS DE, 1991, HISTOL HISTOPATHOL, V6, P525 SINGH A, 1990, ANAL ENV TOXICANTS, P13 SMITH BJ, 1990, TOXICOL APPL PHARM, V105, P372 STALNEL B, 1989, ANDROLOGICA, V21, P282 TRAPP M, 1984, FERTIL STERIL, V42, P1465 VANOMMEN B, 1985, BIOCHEM BIOPH RES CO, V126, P25 VANOMMEN B, 1989, TOXICOL APPL PHARM, V100, P517 VILLENEUVE DC, 1984, ARCH ENV CONTAM TOXI, V2, P243; NR: 29; TC: 17; J9: REPROD TOXICOL; PG: 7; GA: KK822

Source type: Electronic(1)

Language

  • English

Subjects

  • PENTACHLOROPHENOL
  • PORPHYRIA
  • radiation
  • Toxicology
  • GERM CELL
  • OVARIAN
  • INVITRO
  • HEXACHLOROBENZENE
  • SURFACE EPITHELIUM
  • Reproductive Biology
  • MONKEY
  • DESTRUCTION
  • Fertilization
Page range
41-47
Host Title
Reproductive Toxicology
Host Abbreviated Title
Reprod.Toxicol.
Volume
7
Issue
1
ISSN
0890-6238

Department