1997
DOI: 10.1016/s0024-3205(97)00613-9
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Effect of melatonin on serum cholesterol and phospholipid levels, and on prolactin, thyroid-stimulating hormone and thyroid hormone levels, in hyperprolactinemic rats

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Cited by 36 publications
(26 citation statements)
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“…Indeed, as shown in animal studies, several mechanisms can be responsible for the hypolipidemic effects of melatonin, e.g. decrease in intestinal cholesterol absorption [56], inhibition of cholesterol biosynthesis and interaction with LDL cholesterol receptors [57] or augmentation of lecithin-cholesterol acyltransferase-mediated cholesterol esterification [58]. Melatonin ameliorates nonalcoholic fatty liver induced by a high-fat diet in rats that may also affect serum lipids [59].…”
Section: Clinical Studies Using Melatonin In Msmentioning
confidence: 99%
“…Indeed, as shown in animal studies, several mechanisms can be responsible for the hypolipidemic effects of melatonin, e.g. decrease in intestinal cholesterol absorption [56], inhibition of cholesterol biosynthesis and interaction with LDL cholesterol receptors [57] or augmentation of lecithin-cholesterol acyltransferase-mediated cholesterol esterification [58]. Melatonin ameliorates nonalcoholic fatty liver induced by a high-fat diet in rats that may also affect serum lipids [59].…”
Section: Clinical Studies Using Melatonin In Msmentioning
confidence: 99%
“…In genetically and diet-induced hypercholesterolemic rats MEL administration decreased serum cholesterol (Aoyama et al 1988;Mori et al 1989). Esquifino et al (1997) recorded a decrease in cholesterol in the serum, liver, adrenal glands and testes after pineal extract administration to hyperprolactinemic rats while pinealectomy had the opposite effect. Pharmacological doses of MEL administered in tap water during a period of 3 months reduced increased concentrations of total and LDL-cholesterol and increased plasma HDLcholesterol in young rats fed hypercholesterolemic diet.…”
mentioning
confidence: 94%
“…It has also been shown that the ability of LCAT to esterify F-Chol in the plasma of ANIT-treated rats with cholestasis is reduced by a defect of Apo A-1 activation [4]. Esquifino et al [9] reported that a decrease in F-Chol concentration occurs with a concomitant increase in the percentage of E-Chol concentration to T-Chol concentration, in the serum of normal rats injected with MT for 4 days, although there is no change in serum T-Chol concentration. Therefore, there is a possibility that a single oral administration of MT to ANIT-treated rats attenuates the reduced ability to convert F-Chol to E-Chol via LCAT activated by Apo A-1 in the serum.…”
Section: Discussionmentioning
confidence: 99%