Male Reproductive Function
DOI: 10.1007/978-0-585-38145-9_2
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Spermatogenesis and Germ Cell Death

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Cited by 5 publications
(3 citation statements)
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“…31−33 Virtually all sperm in the cauda epididymis of 100 μg/kg treated rats showed severe ultrastructural defects including chromatin decondensation and complete absence of the plasma membrane over the entire tail as well as vacuolated mitochondria. 31,33 However, in reversibility studies, only four of the six triptolide-treated rats had successful matings 14 weeks after treatment cessation, while all 6 rats from the control group remained fertile. 33 These studies found no differences in body weight or weights of reproductive organs, and no discernible effect on plasma levels of luteinizing hormone (LH), follicle-stimulating hormone (FSH), or testosterone at high or low dose, suggesting a nonhormonal mechanism of action.…”
Section: ■ Methodsmentioning
confidence: 99%
“…31−33 Virtually all sperm in the cauda epididymis of 100 μg/kg treated rats showed severe ultrastructural defects including chromatin decondensation and complete absence of the plasma membrane over the entire tail as well as vacuolated mitochondria. 31,33 However, in reversibility studies, only four of the six triptolide-treated rats had successful matings 14 weeks after treatment cessation, while all 6 rats from the control group remained fertile. 33 These studies found no differences in body weight or weights of reproductive organs, and no discernible effect on plasma levels of luteinizing hormone (LH), follicle-stimulating hormone (FSH), or testosterone at high or low dose, suggesting a nonhormonal mechanism of action.…”
Section: ■ Methodsmentioning
confidence: 99%
“…11 Because its anti-fertility was, for its short period of exposure, found to be selective and reversible, triptolide was originally recognized as a potential post-testicular male contraceptive agent. 11,126,127 However, the long-term administration of triptolide in one animal study led to deleterious effects on spermatogenesis and irreversible infertility even after cessation of the treatment. 128 Thus, it is critical but difficult to find an optimum dosage at which triptolide could induce reversible infertility without causing permanent impairment of spermatogenesis.…”
Section: Anti-fertility Activitymentioning
confidence: 99%
“…Two studies from Swerdloff and colleagues in rats have shown that 0.1 mg kg −1 triptolide (treatment for 70-82 days) only induced subtle change in testis in SD rats, but greatly decreased the cauda epididymal sperm content. 43,44 In this study, consecutive administration of triptolide (0.0625 mg kg −1 -0.125 mg kg −1 ) for 60 days caused severe testis injury in C57BL/6 mice (Fig. S4 †).…”
Section: Discussionmentioning
confidence: 57%