2018
DOI: 10.1016/j.biopha.2018.03.045
|View full text |Cite
|
Sign up to set email alerts
|

Protective effect of Lespedeza cuneata ethanol extract on Bisphenol A-induced testicular dysfunction in vivo and in vitro

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
34
0

Year Published

2018
2018
2024
2024

Publication Types

Select...
9

Relationship

0
9

Authors

Journals

citations
Cited by 16 publications
(34 citation statements)
references
References 52 publications
0
34
0
Order By: Relevance
“…To use as a model for human testicular dysgenesis syndrome, pregnant rats were exposed to DnBP and a suppression of intratesticular testosterone, a focal aggregation of Leyding cells and ectopic Sertoli cells were obtained [27]. Also, the possible molecular mechanism of MnBP was investigated in vitro and even at low dose, an increased Sertoli cells proliferation emerged [28].Among other chemicals, evidence from previous studies showed that also bisphenol A (BPA), a precursor to important plastics like polycarbonates and epoxy resins, could interact with the endocrine system [29,30] and semen quality as well [31,32] even if the present evidence is controversial.According to Lassen et al [33] the association between BPA levels and reproductive hormones would support an anti-androgenic effect with deleterious consequences on motile spermatozoa (−6.7%, confidence interval-CI −11.76/1.63 95%), data confirmed also by Radwan et al [34].BPA induced, in in vivo studies, testicular dysfunction and alteration of Sertoli cell viability [35], testicular apoptosis in male rats [36]; after BPA exposure spermatogenic cells were disorganized and degenerated, spermatids had fragmented pyknotic nuclei and a significant decrease in the rate of proliferation of germ cells was present [37].In an epidemiological survey on 215 young health adults, the urinary BPA levels were significantly and inversely associated with sperm concentration and total sperm count [38]. In recent surveys [39,40] sperm concentration, morphology and motility were negatively associated with BPA urinary levels.…”
mentioning
confidence: 59%
See 1 more Smart Citation
“…To use as a model for human testicular dysgenesis syndrome, pregnant rats were exposed to DnBP and a suppression of intratesticular testosterone, a focal aggregation of Leyding cells and ectopic Sertoli cells were obtained [27]. Also, the possible molecular mechanism of MnBP was investigated in vitro and even at low dose, an increased Sertoli cells proliferation emerged [28].Among other chemicals, evidence from previous studies showed that also bisphenol A (BPA), a precursor to important plastics like polycarbonates and epoxy resins, could interact with the endocrine system [29,30] and semen quality as well [31,32] even if the present evidence is controversial.According to Lassen et al [33] the association between BPA levels and reproductive hormones would support an anti-androgenic effect with deleterious consequences on motile spermatozoa (−6.7%, confidence interval-CI −11.76/1.63 95%), data confirmed also by Radwan et al [34].BPA induced, in in vivo studies, testicular dysfunction and alteration of Sertoli cell viability [35], testicular apoptosis in male rats [36]; after BPA exposure spermatogenic cells were disorganized and degenerated, spermatids had fragmented pyknotic nuclei and a significant decrease in the rate of proliferation of germ cells was present [37].In an epidemiological survey on 215 young health adults, the urinary BPA levels were significantly and inversely associated with sperm concentration and total sperm count [38]. In recent surveys [39,40] sperm concentration, morphology and motility were negatively associated with BPA urinary levels.…”
mentioning
confidence: 59%
“…BPA induced, in in vivo studies, testicular dysfunction and alteration of Sertoli cell viability [35], testicular apoptosis in male rats [36]; after BPA exposure spermatogenic cells were disorganized and degenerated, spermatids had fragmented pyknotic nuclei and a significant decrease in the rate of proliferation of germ cells was present [37].…”
mentioning
confidence: 98%
“…In another study about postnatal exposure to BPA, it was shown that administering different doses of BPA (0, 20 and 40 µg kg-1 day -1) from postnatal Day (PND) 3 to PND21, PND 35 or PND49 effected the meiotic process of germ cells and spermatogenesis (43). In additional, a significant increase in DNA damage to spermatocytes and decrease sperm count and motility was observed, following 12 weeks of BPA (10mg/kg bwt) administration in mice (44). Smilarly, Rahman et al (2017) reported that, toxic effect of gestational BPA exposure (5 mg/kg, and 50 mg/kg bw/day) on motility, capacitation, and motion kinematics of spermatozoa in mice.…”
Section: Bpa Spermatogenesis and Sperm Qualitymentioning
confidence: 98%
“…Oral administration of ethanol extract of L. cuneata in BPA-exposed male mice restored testis weight, sperm count, motility, and testosterone levels; inhibited serum biomarkers and oxidative stress defences such as total cholesterol, triglycerides, HDL/LDL-cholesterol, glucose, FFAs, hs-CRP, angiotensinogen, angiotensin II, GOT, GPT, TBARS, GSH, CAT, and SOD1. In vitro , L. cuneata extract recovered cell viability in BPA-treated TM4 Sertoli cells by attenuating Bax expression and activating caspase 3 and PARP [ 112 ].…”
Section: Bpa and Nutraceuticals: Simultaneous Health Effectsmentioning
confidence: 99%