Sergio Noboru Kuriyama
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Sergio Noboru Kuriyama has a total of 44 co-authors. Here are the top co-authors by number of shared publications:
- Francisco José Roma Paumgartten
FIOCRUZ, Brasil
7 shared publications Ibrahim Chahoud
Department of Toxicology, Institute of Clinical Pharmacology and Toxicology, Campus Benjamin Franklin, Charité University Medical School Berlin, Berlin, Germany
6 shared publicationsChris E. Talsness
Institute of Clinical Pharmacology and Toxicology, Department of Toxicology, Charité University Medical School Berlin, Campus Benjamin Franklin, Berlin, Germany
4 shared publicationsKonstanze Grote
Department of Toxicology, Institute of Clinical Pharmacology and Toxicology, Campus Benjamin Franklin, Charité University Medical School Berlin, Berlin, Germany
4 shared publications- Anderson Joel Martino-Andrade
Laboratory of Reproductive Toxicology, Department of Pharmacology, Federal University of Paraná, Brazil
3 shared publications Simone Wichert Grande
Department of Toxicology, Institute of Clinical Pharmacology and Toxicology, Campus Benjamin Franklin, Charité University Medical School Berlin, Berlin, Germany
3 shared publications
Latest Publications
- 1 August 2016
- Published by Elsevier in Reproductive Toxicology
- Vol. 63, 114-124
Thyroid hormone disruption and cognitive impairment in rats exposed to PBDE during postnatal development
- 1 August 2016
- Published by Elsevier in Reproductive Toxicology
- Vol. 63, 114-124
Thyroid hormone disruption and cognitive impairment in rats exposed to PBDE during postnatal development
- 27 July 2009
- Published by The Royal Society in Philosophical Transactions of the Royal Society B: Biological Sciences
- Vol. 364 (1526) , 2079-2096
Components of plastic: experimental studies in animals and relevance for human health
Components used in plastics, such as phthalates, bisphenol A (BPA), polybrominated diphenyl ethers (PBDE) and tetrabromobisphenol A (TBBPA), are detected in humans. In addition to their utility in plastics, an inadvertent characteristic of these chemicals is the ability to alter the endocrine system. Phthalates function as anti-androgens while the main action attributed to BPA is oestrogen-like activity. PBDE and TBBPA have been shown to disrupt thyroid hormone homeostasis while PBDEs also exhibit anti-androgen action. Experimental investigations in animals indicate a wide variety of effects associated with exposure to these compounds, causing concern regarding potential risk to human health. For example, the spectrum of effects following perinatal exposure of male rats to phthalates has remarkable similarities to the testicular dysgenesis syndrome in humans. Concentrations of BPA in the foetal mouse within the range of unconjugated BPA levels observed in human foetal blood have produced effects in animal experiments. Finally, thyroid hormones are essential for normal neurological development and reproductive function. Human body burdens of these chemicals are detected with high prevalence, and concentrations in young children, a group particularly sensitive to exogenous insults, are typically higher, indicating the need to decrease exposure to these compounds.
- 27 July 2009
- Published by The Royal Society in Philosophical Transactions of the Royal Society B: Biological Sciences
- Vol. 364 (1526) , 2079-2096
Components of plastic: experimental studies in animals and relevance for human health
Components used in plastics, such as phthalates, bisphenol A (BPA), polybrominated diphenyl ethers (PBDE) and tetrabromobisphenol A (TBBPA), are detected in humans. In addition to their utility in plastics, an inadvertent characteristic of these chemicals is the ability to alter the endocrine system. Phthalates function as anti-androgens while the main action attributed to BPA is oestrogen-like activity. PBDE and TBBPA have been shown to disrupt thyroid hormone homeostasis while PBDEs also exhibit anti-androgen action. Experimental investigations in animals indicate a wide variety of effects associated with exposure to these compounds, causing concern regarding potential risk to human health. For example, the spectrum of effects following perinatal exposure of male rats to phthalates has remarkable similarities to the testicular dysgenesis syndrome in humans. Concentrations of BPA in the foetal mouse within the range of unconjugated BPA levels observed in human foetal blood have produced effects in animal experiments. Finally, thyroid hormones are essential for normal neurological development and reproductive function. Human body burdens of these chemicals are detected with high prevalence, and concentrations in young children, a group particularly sensitive to exogenous insults, are typically higher, indicating the need to decrease exposure to these compounds.
- Open Access
- 1 March 2008
- Published by American Chemical Society (ACS) in Environmental Health Perspectives
- Vol. 116 (3) , 308-314
In Utero and Lactational Exposures to Low Doses of Polybrominated Diphenyl Ether-47 Alter the Reproductive System and Thyroid Gland of Female Rat Offspring
Background: Polybrominated diphenyl ethers (PBDEs) are capable of disrupting thyroid hormone homeostasis. PBDE-47 (2,2′,4,4′-tetrabromodiphenyl ether) is one of the most abundant congeners found in human breast adipose tissue and maternal milk samples. Objectives: We evaluated the effects of developmental exposure to low doses of PBDE-47 on the female reproductive system. Methods: Pregnant Wistar rats were administered vehicle (peanut oil) or PBDE-47 [140 or 700 μg/kg body weight (bw)] on gestation day (GD) 6, or 5 mg 6-n-propyl-2-thiouracil (PTU)/L in the drinking water from GD7 through postnatal day (PND) 21. Results: In female offspring sacrificed on PND38, there was a significant decrease in ovarian weight after exposure to PTU or 140 μg/kg PBDE-47. Alterations in folliculogenesis were apparent: we observed a decrease in tertiary follicles and serum estradiol concentrations in the offspring exposed to either PTU or 700 μg/kg PBDE-47. PTU exposure also resulted in a decrease in primordial follicles. On PND100, persistent effects on the thyroid glands included histologic and morphometric changes after exposure to either PTU or PBDE-47. No relevant changes in reproductive indices were observed after mating the exposed F1 females with nontreated males. Conclusions: Administration of PBDE-47 at doses relevant to human exposure led to changes in the rat female reproductive system and thyroid gland.
- 1 March 2008
- Published by American Chemical Society (ACS) in Environmental Health Perspectives
- Vol. 116 (3) , 308-314
Open AccessIn Utero and Lactational Exposures to Low Doses of Polybrominated Diphenyl Ether-47 Alter the Reproductive System and Thyroid Gland of Female Rat Offspring
Background: Polybrominated diphenyl ethers (PBDEs) are capable of disrupting thyroid hormone homeostasis. PBDE-47 (2,2′,4,4′-tetrabromodiphenyl ether) is one of the most abundant congeners found in human breast adipose tissue and maternal milk samples. Objectives: We evaluated the effects of developmental exposure to low doses of PBDE-47 on the female reproductive system. Methods: Pregnant Wistar rats were administered vehicle (peanut oil) or PBDE-47 [140 or 700 μg/kg body weight (bw)] on gestation day (GD) 6, or 5 mg 6-n-propyl-2-thiouracil (PTU)/L in the drinking water from GD7 through postnatal day (PND) 21. Results: In female offspring sacrificed on PND38, there was a significant decrease in ovarian weight after exposure to PTU or 140 μg/kg PBDE-47. Alterations in folliculogenesis were apparent: we observed a decrease in tertiary follicles and serum estradiol concentrations in the offspring exposed to either PTU or 700 μg/kg PBDE-47. PTU exposure also resulted in a decrease in primordial follicles. On PND100, persistent effects on the thyroid glands included histologic and morphometric changes after exposure to either PTU or PBDE-47. No relevant changes in reproductive indices were observed after mating the exposed F1 females with nontreated males. Conclusions: Administration of PBDE-47 at doses relevant to human exposure led to changes in the rat female reproductive system and thyroid gland.
- 1 December 2007
- Published by Elsevier in Toxicology
- Vol. 242 (1-3) , 80-90
Developmental exposure to low-dose PBDE-99: Tissue distribution and thyroid hormone levels
- 1 December 2007
- Published by Elsevier in Toxicology
- Vol. 242 (1-3) , 80-90
Developmental exposure to low-dose PBDE-99: Tissue distribution and thyroid hormone levels
- 1 May 2006
- Published by Elsevier in Toxicology
- Vol. 222 (1-2) , 17-24
Effects of peripubertal exposure to triphenyltin on female sexual development of the rat
- 1 May 2006
- Published by Elsevier in Toxicology
- Vol. 222 (1-2) , 17-24
Effects of peripubertal exposure to triphenyltin on female sexual development of the rat
- 1 July 2005
- Published by Elsevier in Toxicology Letters
- Vol. 157 (3) , 189-202
Ultrastructural changes observed in rat ovaries following in utero and lactational exposure to low doses of a polybrominated flame retardant
- 1 July 2005
- Published by Elsevier in Toxicology Letters
- Vol. 157 (3) , 189-202
Ultrastructural changes observed in rat ovaries following in utero and lactational exposure to low doses of a polybrominated flame retardant
- Open Access
- 1 February 2005
- Published by American Chemical Society (ACS) in Environmental Health Perspectives
- Vol. 113 (2) , 149-154
Developmental Exposure to Low-Dose PBDE-99: Effects on Male Fertility and Neurobehavior in Rat Offspring
In utero exposure to a single low dose of 2,2′,4,4′,5-pentabromodiphenyl ether (PBDE-99) disrupts neurobehavioral development and causes permanent effects on the rat male reproductive system apparent in adulthood. PBDEs, a class of flame ...
- 1 February 2005
- Published by American Chemical Society (ACS) in Environmental Health Perspectives
- Vol. 113 (2) , 149-154
Open AccessDevelopmental Exposure to Low-Dose PBDE-99: Effects on Male Fertility and Neurobehavior in Rat Offspring
In utero exposure to a single low dose of 2,2′,4,4′,5-pentabromodiphenyl ether (PBDE-99) disrupts neurobehavioral development and causes permanent effects on the rat male reproductive system apparent in adulthood. PBDEs, a class of flame ...
- 1 October 2004
- Published by Elsevier in Toxicology
- Vol. 202 (3) , 185-197
In utero exposure to low-dose 2,3′,4,4′,5-pentachlorobiphenyl (PCB 118) impairs male fertility and alters neurobehavior in rat offspring
- 1 October 2004
- Published by Elsevier in Toxicology
- Vol. 202 (3) , 185-197
In utero exposure to low-dose 2,3′,4,4′,5-pentachlorobiphenyl (PCB 118) impairs male fertility and alters neurobehavior in rat offspring
- 6 September 2003
- Published by Elsevier in Toxicology Letters
- Vol. 145 (2) , 175-180
Absence of tumor promoting activity of Euphorbia milii latex on the mouse back skin
- 6 September 2003
- Published by Elsevier in Toxicology Letters
- Vol. 145 (2) , 175-180
Absence of tumor promoting activity of Euphorbia milii latex on the mouse back skin
- 1 April 2003
- Published by Elsevier in Toxicology
- Vol. 186 (1-2) , 11-20
Effect of low dose mono-ortho 2,3′,4,4′,5 pentachlorobiphenyl on thyroid hormone status and EROD activity in rat offspring: consequences for risk assessment
- 1 April 2003
- Published by Elsevier in Toxicology
- Vol. 186 (1-2) , 11-20
Effect of low dose mono-ortho 2,3′,4,4′,5 pentachlorobiphenyl on thyroid hormone status and EROD activity in rat offspring: consequences for risk assessment