2018
DOI: 10.1016/j.aquatox.2018.02.006
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Gemfibrozil and carbamazepine decrease steroid production in zebrafish testes ( Danio rerio )

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Cited by 33 publications
(26 citation statements)
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“…These authors also examined the molecular effects of gemfibrozil and atorvastatin on their fish specimens, demonstrating: (1) the up-regulation of PPARA, coding for the peroxisome proliferator-activated receptor α in the females, but not the males, which is consistent with the greater reduction in the triglyceride levels, (2) the drug-induced upregulation of PPARG, coding for the Peroxisome proliferator-activated receptor γ, (3) the atorvastatin-triggered up-regulation of SREPB1 (sterol regulatory element-binding protein), coding for a transcriptional activator of fatty acids and the triglyceride synthesis, (4) the drug-induced, male-specific up-regulation of CYP3A6, coding for the cytochrome P450 3A6 protein involved in the detoxification of endogenous substances and xenobiotics and ( 5) the drug-induced, male-specific up-regulation of Atrogin-1, whose protein product is responsible for resistance to the toxic effect of statins. Fraz et al [169] and Galus et al [170] revealed the same findings, confirming the inhibition effects of gemfibrozil on 11-ketotestosterone in their male and female specimens (Table 3, Figure 3). These studies highlighted gender-dependent effects, substantiating a lipid-lowering role played by these drugs in the zebrafish species.…”
Section: Antidyslipidemicssupporting
confidence: 70%
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“…These authors also examined the molecular effects of gemfibrozil and atorvastatin on their fish specimens, demonstrating: (1) the up-regulation of PPARA, coding for the peroxisome proliferator-activated receptor α in the females, but not the males, which is consistent with the greater reduction in the triglyceride levels, (2) the drug-induced upregulation of PPARG, coding for the Peroxisome proliferator-activated receptor γ, (3) the atorvastatin-triggered up-regulation of SREPB1 (sterol regulatory element-binding protein), coding for a transcriptional activator of fatty acids and the triglyceride synthesis, (4) the drug-induced, male-specific up-regulation of CYP3A6, coding for the cytochrome P450 3A6 protein involved in the detoxification of endogenous substances and xenobiotics and ( 5) the drug-induced, male-specific up-regulation of Atrogin-1, whose protein product is responsible for resistance to the toxic effect of statins. Fraz et al [169] and Galus et al [170] revealed the same findings, confirming the inhibition effects of gemfibrozil on 11-ketotestosterone in their male and female specimens (Table 3, Figure 3). These studies highlighted gender-dependent effects, substantiating a lipid-lowering role played by these drugs in the zebrafish species.…”
Section: Antidyslipidemicssupporting
confidence: 70%
“…The different trends of these enzymatic activities, which have been shown to be concentration dependent, are probably due to a condition of high oxidative stress at high exposure concentrations with a consequential suffering of the organism, unlike the lower concentrations in which the antioxidant system still responds to increase the levels of enzyme released into the circulation. Beyond this, carbamazepine (10 µg/L) also had an inhibiting effect on 11-ketotestosterone levels in the whole body, the plasma and the tests of male fishes after 67 days of drug exposure [169]. The authors suggested that there is an impact on testicular androgen production in zebrafish after chronic exposure, but it seems more probably a general effect in the organism due to stress and cell death, rather than a pure endocrine response.…”
Section: Antiepileptics and Antipsychoticsmentioning
confidence: 99%
“…As vertebrates, fish are perhaps more susceptible to pharmaceutical exposure than invertebrates because pharmaceuticals are designed for human (vertebrate) use. Data on the toxic effects of CBZ on fish have been reported for different species, such as the zebrafish (Danio rerio), Chinese rare minnows (Gobiocypris rarus), and Japanese medaka (Oryzia latipeus) [15][16][17][18][19][20]. For example, 0.5 µg/L CBZ exposure increased embryo mortality, lowered plasma steroid hormone levels, and decreased egg production in zebrafish [21].…”
Section: Introductionmentioning
confidence: 99%
“…All these studies show that caffeine besides to be an anthropogenic marker, is an emerging contaminant and thus assessing exposure to a given risk is important to ensure the integrity of human health and the diversity of aquatic ecosystems [34][35][36] .…”
Section: Caffeine As An Emerging Contaminant: Concentrations and Ecotmentioning
confidence: 99%