Literature DB >> 6834175

The morphological development of di-N-pentyl phthalate induced testicular atrophy in the rat.

D M Creasy, J R Foster, P M Foster.   

Abstract

Prepubertal rats treated orally with di-n-pentyl phthalate at 2.2 g/kg body weight were killed at 1, 3, 6 and 24 hr following a single dose, and after 2, 3 and 4 days of repeated daily dosing. At 3 hr Sertoli cells in a proportion of the seminiferous tubules showed vacuolation of the perinuclear smooth endoplasmic reticulum with an associated inward displacement of germinal cells. By 6 hr the vacuolation had extended to the apical cytoplasm and was evident in most tubules. Early degenerative changes were also apparent in spermatocytes and spermatids and were accompanied by an acute interstitial inflammatory infiltrate. By 24 hr, germinal cell degeneration was extensive with desquamation and general disorganisation of cell layers within the epithelium, but the interstitial inflammatory infiltrate had declined. Mitochondrial succinic dehydrogenase activity in Sertoli cells was reduced at 3 and 6 hr and absent by 24 hr. In germinal cells it was unaffected at 3 and 6 hr but absent by 24 hr. Two, three and four days of daily phthalate treatment resulted in a gradual depletion of germinal cells from all tubules, leaving a Sertoli cell matrix containing a few necrotic spermatocytes and occasional normal spermatogonia. The significance of the early Sertoli cell changes is discussed.

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Year:  1983        PMID: 6834175     DOI: 10.1002/path.1711390307

Source DB:  PubMed          Journal:  J Pathol        ISSN: 0022-3417            Impact factor:   7.996


  16 in total

1.  Dose-dependent effect of phthalate ester on testicular descent in pre-and post natal rats.

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2.  Gonad histology and vitellogenin concentrations in brown trout (Salmo trutta) from Danish streams impacted by sewage effluent.

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3.  Dipentyl phthalate dosing during sexual differentiation disrupts fetal testis function and postnatal development of the male Sprague-Dawley rat with greater relative potency than other phthalates.

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Journal:  Toxicol Sci       Date:  2010-12-20       Impact factor: 4.849

4.  A short-term in vivo screen using fetal testosterone production, a key event in the phthalate adverse outcome pathway, to predict disruption of sexual differentiation.

Authors:  Johnathan R Furr; Christy S Lambright; Vickie S Wilson; Paul M Foster; Leon E Gray
Journal:  Toxicol Sci       Date:  2014-05-05       Impact factor: 4.849

5.  Male infertility, impaired spermatogenesis, and azoospermia in mice deficient for the pseudophosphatase Sbf1.

Authors:  Ron Firestein; Peter L Nagy; Megan Daly; Phil Huie; Marco Conti; Michael L Cleary
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6.  Urinary creatine profiles after administration of cell-specific testicular toxicants to the rat.

Authors:  N P Moore; D M Creasy; T J Gray; J A Timbrell
Journal:  Arch Toxicol       Date:  1992       Impact factor: 5.153

7.  Effects of repeated intravenous infusions of the plasticizer di-(2-ethylhexyl) phthalate in young male rats.

Authors:  P Sjöberg; N G Lindquist; G Montin; L Plöen
Journal:  Arch Toxicol       Date:  1985-12       Impact factor: 5.153

8.  Effects of intravenous and oral di(2-ethylhexyl) phthalate (DEHP) and 20% Intralipid vehicle on neonatal rat testis, lung, liver, and kidney.

Authors:  Luísa Camacho; John R Latendresse; Levan Muskhelishvili; Charles D Law; K Barry Delclos
Journal:  Food Chem Toxicol       Date:  2020-06-13       Impact factor: 6.023

Review 9.  Signaling pathways in spermatogonial stem cells and their disruption by toxicants.

Authors:  Benjamin Lucas; Christopher Fields; Marie-Claude Hofmann
Journal:  Birth Defects Res C Embryo Today       Date:  2009-03

10.  MEHP-induced rat testicular inflammation does not exacerbate germ cell apoptosis.

Authors:  Jorine J L P Voss; Angela R Stermer; Rashin Ghaffari; Richa Tiwary; John H Richburg
Journal:  Reproduction       Date:  2018-05-09       Impact factor: 3.906

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