Lack of Protective Effect of D-003, a Mixture of High-Molecular-Weight Primary Acids from Sugar Cane Wax, on Liver Damage Induced by Galactosamine in Rats
Abstract:D-003 is a mixture of very-high-molecular-weight aliphatic primary acids purified from sugar cane wax, wherein octacosanoic acid is the most abundant. Experimental and clinical studies have shown that D-003 lowers cholesterol and prevents plasma lipoprotein peroxidation (LP). D-003 has protected against the histological changes characteristic of CCl4- and paracetamol-induced hepatic injury in rats, in which LP plays a pivotal role for explaining the resulting hepatotoxicity. Galactosamine induces hepatotoxicit… Show more
“…It has been shown that when octacosanol (60 mg/kg BW) is orally administered to rats, not only octacosanol but also octacosanoic acid, an oxidation product of octacosanol, appears in the liver and the hepatic amount of octacosanoic acid is a few times higher than that of octacosanol [ 35 ]. Noa et al [ 36 ] reported that oral administration of D-003, a mixture of high molecular weight primary acids, such as octacosanoic acid, purified from sugar cane wax, protected against CCl 4 -induced acute liver injury in rats. In addition, it is known that LDL prepared from rats administered with D-003 is less susceptible to in vitro lipid peroxidation induced by copper ion and a free radical generator, 2,2'-azobis(2-amidinopropane), than LDL from rats without D-003 administration [ 37 ], like the case of administered policosanol [ 1 , 2 ].…”
Summary We examined whether octacosanol, the main component of policosanol, attenuates disrupted hepatic reactive oxygen species metabolism associated with acute liver injury progression in rats intoxicated with carbon tetrachloride (CCl4). In rats intoxicated with CCl4 (1 ml/kg, i.p.), the activities of serum transaminases increased 6 h after intoxication and further increased at 24 h. In the liver of CCl4-intoxicated rats, increases in lipid peroxide (LPO) concentration and myeloperoxidase activity and decreases in superoxixde dismutase activity and reduced glutathione (GSH) concentration occurred 6 h after intoxication and these changes were enhanced with an increase in xanthine oxidase activity and a decrease in catalase activity at 24 h. Octacosanol (10, 50 or 100 mg/kg) administered orally to CCl4-intoxicated rats at 6 h after intoxication attenuated the increased activities of serum transaminases and the increased hepatic myeloperoxidase and xanthine oxidase activities and LPO concentration and the decreased hepatic superoxide dismutase and catalase activities and GSH concentration found at 24 h after intoxication dose-dependently. Octacosanol (50 or 100 mg/kg) administered to untreated rats decreased the hepatic LPO concentration and increased the hepatic GSH concentration. These results indicate that octacosanol attenuates disrupted hepatic reactive oxygen species metabolism associated with acute liver injury progression in CCl4-intoxicated rats.
“…It has been shown that when octacosanol (60 mg/kg BW) is orally administered to rats, not only octacosanol but also octacosanoic acid, an oxidation product of octacosanol, appears in the liver and the hepatic amount of octacosanoic acid is a few times higher than that of octacosanol [ 35 ]. Noa et al [ 36 ] reported that oral administration of D-003, a mixture of high molecular weight primary acids, such as octacosanoic acid, purified from sugar cane wax, protected against CCl 4 -induced acute liver injury in rats. In addition, it is known that LDL prepared from rats administered with D-003 is less susceptible to in vitro lipid peroxidation induced by copper ion and a free radical generator, 2,2'-azobis(2-amidinopropane), than LDL from rats without D-003 administration [ 37 ], like the case of administered policosanol [ 1 , 2 ].…”
Summary We examined whether octacosanol, the main component of policosanol, attenuates disrupted hepatic reactive oxygen species metabolism associated with acute liver injury progression in rats intoxicated with carbon tetrachloride (CCl4). In rats intoxicated with CCl4 (1 ml/kg, i.p.), the activities of serum transaminases increased 6 h after intoxication and further increased at 24 h. In the liver of CCl4-intoxicated rats, increases in lipid peroxide (LPO) concentration and myeloperoxidase activity and decreases in superoxixde dismutase activity and reduced glutathione (GSH) concentration occurred 6 h after intoxication and these changes were enhanced with an increase in xanthine oxidase activity and a decrease in catalase activity at 24 h. Octacosanol (10, 50 or 100 mg/kg) administered orally to CCl4-intoxicated rats at 6 h after intoxication attenuated the increased activities of serum transaminases and the increased hepatic myeloperoxidase and xanthine oxidase activities and LPO concentration and the decreased hepatic superoxide dismutase and catalase activities and GSH concentration found at 24 h after intoxication dose-dependently. Octacosanol (50 or 100 mg/kg) administered to untreated rats decreased the hepatic LPO concentration and increased the hepatic GSH concentration. These results indicate that octacosanol attenuates disrupted hepatic reactive oxygen species metabolism associated with acute liver injury progression in CCl4-intoxicated rats.
“…During the last years, sugarcane has raised interest regarding its nutraceutic properties. Several studies have shown beneficial effects of sugarcane extracts on models in vivo in the stimulation of the immune response, protection against liver damage, intestinal function recovery, protection against some infections, antitrombotic and antistress effects or growth stimulation (Koge et al ., ; Noa et al ., ; El‐Abasy et al ., , ; Amer et al ., ; Lo et al ., ; Motobu et al ., ; Yamauchi et al ., ). On searching the origin of these beneficial effects, it has been found that sugarcane has a powerful antioxidant activity (Abbas et al ., ; Feng et al ., ), and it is known that oxidative damage is involved in many human diseases such as cancer, cardiovascular diseases or other degenerative disorders.…”
Summary
Antioxidant properties of commercial sugarcane‐derived products were analysed to study their suitability for being used as functional ingredients. Cane honey, several jaggeries and several brown sugars were selected from the market and analysed in terms of physicochemical characteristics and antioxidant properties, and compared with white refined sugar (twelve products in total). Moisture, water activity, total soluble solids, pH, colour and sugar profile are reported. As for antioxidant properties, total phenols and flavonoid content, as well as antiradical ability (DPPH˙ and the TEAC‐ABTS methods), are given. All sugarcane products contained phenols and flavonoids and exhibited in vitro antioxidant activity, determined by degree of refining. Among the alternatives analysed, jaggeries and cane honey showed the best antioxidant properties. Thermal treatment did not significantly affect the antioxidant capacity of sugarcane products, especially jaggeries. As sugar‐rich products are widely consumed worldwide, the use of non‐refined sugarcane derivatives in food formulation is encouraged.
“…Some investigators [2,3] have consistently proved on in vivo models the antioxidant properties of high molecular weight alcohols contained in the wax. Sugar cane also contains phenolic acids, flavonoids and other phenolic compounds [4,5], which could account for certain antioxidant activity.…”
Phenolic compounds in sugar cane (Saccharum officinarum L.) juice were identified and quantified by analytical high performance liquid chromatography and photodiode array detection, showing the predominance of flavones (apigenin, luteolin and tricin derivatives), among flavonoids, and of hydroxycinnamic, caffeic and sinapic acids, among phenolic acids, representing a total content of around 160 mg/L. A tricin derivative was present in the highest proportion (>10% of the total). The phenolic extract obtained from sugar cane juice showed a protective effect against in vivo MeHgCl intoxication and potent inhibition of ex vivo lipoperoxidation of rat brain homogenates, indicating a potential use for beneficial health effects and/or therapeutic applications.
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