2013
DOI: 10.1080/00207233.2013.810854
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Protective effect of D-psicose against testicular atrophy induced by di(2-ethylhexyl) phthalate

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Cited by 3 publications
(4 citation statements)
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“…Therefore, MEHP is considered to be a substance directly involved in testicular toxicity [18][19][20]. In our studies, plasma or testicular MEHP concentrations were closely associated with the degree of testicular atrophy [25,26,[45][46][47]. In addition, 4-week-old rats showed higher susceptibility than 5-week-old rats.…”
Section: Dehp-induced Testicular Atrophy In Ratsmentioning
confidence: 82%
See 1 more Smart Citation
“…Therefore, MEHP is considered to be a substance directly involved in testicular toxicity [18][19][20]. In our studies, plasma or testicular MEHP concentrations were closely associated with the degree of testicular atrophy [25,26,[45][46][47]. In addition, 4-week-old rats showed higher susceptibility than 5-week-old rats.…”
Section: Dehp-induced Testicular Atrophy In Ratsmentioning
confidence: 82%
“…Furthermore, testicular MDA production after oral administration of 2 g/kg DEHP was almost suppressed by pretreatment with 4% D-allulose water or 4% D-allose water (Figure 3). Furthermore, D-allulose water with a concentration of 2% or more showed almost complete protection against DEHP (1 w/w %) diet -induced testicular atrophy for up to 2 weeks (Figure 4, 5) [25,[45][46][47]. As shown in Figure 6, testis sections from DEHP-only given rats showed degeneration of the seminiferous tubules and sloughing of germ cells into the tubular lumen.…”
Section: Protective Potency Of D-allulosementioning
confidence: 99%
“…DEHP administered orally is rapidly hydrolyzed by pancreatic lipase [24] and mucosal esterase [25] in the gastrointestinal tract to mono-(2ethylhexyl) phthalate (MEHP), which is the most toxic metabolite of DEHP. MEHP has been shown to be a direct acting agent that disrupts the function of Sertoli and Leydig cells and also induces oxidative stress in the germ cells [26,27,20] leading to cellular apoptosis. On the other hand, ethanol is known to have a hydroxyl radical scavenging effect [28][29][30][31].…”
Section: Discussionmentioning
confidence: 99%
“…Many studies have shown the toxic effects of DEHP on male reproductive organs in the rodents at growth stages [9][10][11][12][13][14][15][16][17][18][19]. Although the pathogenesis of testicular atrophy by DEHP is yet unclear, this injury has been suggested to be due to oxidative stress induced by mono (2-ethylhexyl) phthalate (MEHP), a metabolite of DEHP [20].…”
Section: Introductionmentioning
confidence: 99%