TY - JOUR
T1 - Mono-(2-ethylhexyl) phthalate targets glycogen debranching enzyme and affects glycogen metabolism in rat testis
AU - Kuramori, Chikanori
AU - Hase, Yasuyoshi
AU - Hoshikawa, Koichi
AU - Watanabe, Keiko
AU - Nishi, Takeyuki
AU - Hishiki, Takako
AU - Soga, Tomoyoshi
AU - Nashimoto, Akihiro
AU - Kabe, Yasuaki
AU - Yamaguchi, Yuki
AU - Watanabe, Hajime
AU - Kataoka, Kohsuke
AU - Suematsu, Makoto
AU - Handa, Hiroshi
N1 - Funding Information:
Special Coordination Funds for Promoting Science and Technology from the Japan Science and Technology Agency; Grant from the Global COE Program from the Ministry of Education, Culture, Sports, Science and Technology; and grant from NEDO to H.H.
PY - 2009
Y1 - 2009
N2 - Phthalate esters are commonly used plasticizers; however, some are suspected to cause reproductive toxicity. Administration of high doses of di-(2-ethylhexyl) phthalate (DEHP) induces germ cell death in male rodents. Mono-(2-ethylhexyl) phthalate (MEHP), a hydrolyzed metabolite of DEHP, appears to be responsible for this testicular toxicity; however, the underlying mechanism of this chemical's action remains unknown. Here, using a one-step affinity purification procedure, we identified glycogen debranching enzyme (GDE) as a phthalate-binding protein. GDE has oligo-1,4-1,4-glucanotransferase and amylo-1,6-glucosidase activities, which are responsible for the complete degradation of glycogen to glucose. Our findings demonstrate that MEHP inhibits the activity of oligo-1,4-1,4-glucanotransferase, but not of amylo-1,6-glucosidase. Among various phthalate esters tested, MEHP specifically binds to and inhibits GDE. We also show that DEHP administration affects glycogen metabolism in rat testis. Thus, inhibition of GDE by MEHP may play a role in germ cell apoptosis in the testis.
AB - Phthalate esters are commonly used plasticizers; however, some are suspected to cause reproductive toxicity. Administration of high doses of di-(2-ethylhexyl) phthalate (DEHP) induces germ cell death in male rodents. Mono-(2-ethylhexyl) phthalate (MEHP), a hydrolyzed metabolite of DEHP, appears to be responsible for this testicular toxicity; however, the underlying mechanism of this chemical's action remains unknown. Here, using a one-step affinity purification procedure, we identified glycogen debranching enzyme (GDE) as a phthalate-binding protein. GDE has oligo-1,4-1,4-glucanotransferase and amylo-1,6-glucosidase activities, which are responsible for the complete degradation of glycogen to glucose. Our findings demonstrate that MEHP inhibits the activity of oligo-1,4-1,4-glucanotransferase, but not of amylo-1,6-glucosidase. Among various phthalate esters tested, MEHP specifically binds to and inhibits GDE. We also show that DEHP administration affects glycogen metabolism in rat testis. Thus, inhibition of GDE by MEHP may play a role in germ cell apoptosis in the testis.
KW - Germ cell
KW - Glycogen debranching enzyme
KW - Glycogen metabolism
KW - Metabolome analysis
KW - Phthalate esters
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U2 - 10.1093/toxsci/kfp041
DO - 10.1093/toxsci/kfp041
M3 - Article
C2 - 19240039
AN - SCOPUS:65549121653
SN - 1096-6080
VL - 109
SP - 143
EP - 151
JO - Toxicological Sciences
JF - Toxicological Sciences
IS - 1
ER -