Fertility and early embryonic development toxicity and toxicokinetic study of KFP‐H008 in Sprague–Dawley rats
Исследование токсичности для фертильности и раннего эмбрионального развития и токсикокинетики KFP‑H008 у крыс линии Sprague–Dawley
2022-03-12
SCID: 54.1/rk9xcwhd
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KFP-H008Sprague–Dawley ratsfertility and early embryonic development toxicitypotassium competitive acid blockertoxicokinetics (TK)
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Abstract (AI)
The novel potassium competitive acid blocker, KFP-H008, developed to overcome the shortcomings of proton pump inhibitors. In this study, KFP-H008 was administered by oral gavage at doses of 0 (control), 15, 45, and 150 mg/kg to Sprague-Dawley rats (24 animals per sex per group). Body weight, food consumption, mortality, sexual cycle, mating behavior, pregnancy, sperm motility, and relative organ weights were evaluated. In a concomitant toxicokinetic (TK) study (10 animals per sex per group), plasma TK parameters and tissue distribution of KFP-H008 were tested. There were obvious effects at the dosage of 150 mg/kg to male rats with decreases of prostate weight and lower weight gain; to female rats with lower weight gain, hair off, and lower corpus luteum count. There were no effects on litter parameters. Time to reach maximum plasma concentrations for KFP-H008 was between 0.5 and 1.0 hr for the 15 and 45 mg/kg groups, while for the 150 mg/kg group it had a delay to 2 hr. Overall, the NOAEL of KFP-H008 was considered to be 45 mg/kg in both genders and the TK study shows that exposure (area under the curve) of male rats was about 1,091.0 ± 530.8 μg/Lhr and to female rats was 1,030.5 ± 512.5 μg/Lhr. Administration of KFP-H008although reaches the reproductive organs, it demonstrated no significant effects on reproductive organs, it did not affect mating, fertility, pregnancy, growth, or morphologic development.
Key Findings
1
KFP-H008 administered orally at 0, 15, 45, and 150 mg/kg to Sprague–Dawley rats produced clear adverse effects at 150 mg/kg but not at lower doses.
2
Male rats at 150 mg/kg showed decreased prostate weight and reduced body weight gain; female rats at 150 mg/kg showed reduced body weight gain, hair loss, and lower corpus luteum count.
3
No effects of KFP-H008 were observed on litter parameters, mating, fertility, pregnancy, growth, or morphological development of offspring.
4
The systemic NOAEL (no-observed-adverse-effect level) for both sexes was determined to be 45 mg/kg, with TK exposure (AUC) approximately 1,091.0 ± 530.8 μg·L⁻¹·hr in males and 1,030.5 ± 512.5 μg·L⁻¹·hr in females.
5
Time to maximum plasma concentration was 0.5–1.0 hr for 15 and 45 mg/kg, delayed to 2 hr at 150 mg/kg.
Research Object
KFP-H008 administered orally to Sprague–Dawley rats
Research Subject
Fertility and early embryonic development toxicity and toxicokinetics (plasma TK parameters and tissue distribution), plus effects on body/organ weights, mating, pregnancy, and reproductive parameters
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2022-03-12
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References available in scid.ai3
Cytochrome P450-Based Drug-Drug Interactions of Vonoprazan In Vitro and In Vivo2020
Potent Potassium-competitive Acid Blockers: A New Era for the Treatment of Acid-related Diseases2018
Effective and safe proton pump inhibitor therapy in acid-related diseases – A position paper addressing benefits and potential harms of acid suppression2016