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. 2020 Aug 19;2:100022. doi: 10.1016/j.sleepx.2020.100022

Table 1.

Summary of toxicity studies with melatonin. SD: single Dose. LT: long-term administration. GT: genotoxicity. CG: carcinogenicity. O: other toxicity studies. i.p.: intraperitoneally, s.c. subcutaneously, i.v. intravenously. dw: drinking water.

Study type Animal Route Duration Results Reference
SD Rats in vivo Orally, i.p.,s.c., i.v. Once-only At doses >400 mg/kg: vasodilatation, piloerection, ptosis, impairment of righting reflex, lack of motor activity, decrease in body temperature and respiratory problems preceding death [109]
LT Aged rats and mice in vivo 10 mg/L in dw 16 months Improved health and survival of aged rats and mice [111,112]
LT Diabetic mice and hypercholestaemia-susceptible rats in vivo s.c or in dw Enhanced survival [114,115]
GT In vitro non-mammalian cell system No mutagenicity in bacterial strains. [113,[116], [117], [118]]
GT In vitro mammalian cell system No chromosome aberrations and no clastogenic activity. Protective anti-clastogenic activity. Nop DNA strand breaks. [113,117,119]
GT In vivo cell system 5 mg/kg s.c. Not mutagenic in mouse bone marrow cells; reduced chromosome aberration rates.
Not mutagenic in mice sperm head anomaly test; reduced sperm head anomaly rates.
[120]
GT In vivo cell system 10 mg/kg i.p. No adverse effects on rat peripheral blood micronucleus test. [121]
GT In vivo study in rats or mice 4–10 mg/kg i.p. Protective effects against genotoxic action of potassium dichromate, cobalt, ethanol, paraquat [[122], [123], [124], [125]]
GT In vitro study using human lymphocytes 0.2 mM Anti-genotoxic effect on mercuric chloride and gossypol [110,126]
CG Transgenic mice at increased risk for prostate adenocarcinoma 10–20 mcg/L in dw 18 weeks Strong prostate cancer inhibitory effect [127]
CG Transgenic mice susceptible for mammary tumours 50–200 mcg/kg per day via gavage 30 weeks Reduced incidence and growth rate of mammary tumours [128,144]
CG Rats, mice susceptible for breast cancer 10–20 mcg/L in dw >1 yr No induction of uterine tumours, lower incidence of mammary tumours. [129,130]