Maksim Sukhov, Tatiana Giro, Sergey Kozlov, Irina Ziruk
{"title":"添加蜂花粉的生腌禽肉:实验动物的生物医学研究","authors":"Maksim Sukhov, Tatiana Giro, Sergey Kozlov, Irina Ziruk","doi":"10.21603/2074-9414-2023-4-2476","DOIUrl":null,"url":null,"abstract":"Natural food additives can fortify meat products. Bee pollen, also known as beebread or ambrosia, contains amino acids, carbohydrates, vitamins, minerals, enzymes, etc. As a result, it possesses numerous therapeutic and prophylactic properties. Bee pollen has good prospects as a fortifying agent for jerky meat, i.e., lean and dehydrated trimmed meat cut into strips. This study tested dry-cured jerky meat fortified with bee pollen on rats with carbon tetrachloride-induced acute toxic hepatitis. The research featured white non-linear laboratory rats. The control group obtained a standard diet. The experimental rats were induced with liver hepatitis by administering CCl4. On day 2, the experimental group was divided into three subgroups: experimental group I (standard diet + traditional jerky), experimental group II (standard diet + jerky fortified with bee pollen), and experimental group III (standard diet), which served as positive control. The research involved a MicroCC20Vet analyzer for hematological tests and a StatFax 3300 analyzer with Diacon DS diagnostic systems for biochemical tests. The histological analyses relied on the method developed by G.A. Merkulov. The hematological parameters demonstrated no changes. As for the biochemistry, experimental groups I and II developed a protein content increase. On day 14, the concentration of protein and its fractions in experimental group II reached the level of intact animals. In experimental groups II and III, the total protein was significantly higher due to the globulin fraction as a result of inflammatory and destructive processes in the liver. However, the rats had normal live weight gain, and their liver demonstrated no histological deviations. In this preclinical study, bee pollen as part of jerky meat formulation had no negative effect on laboratory rats. Bee pollen also proved its antioxidant properties.","PeriodicalId":12335,"journal":{"name":"Food Processing: Techniques and Technology","volume":" 5","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Raw Cured Poultry Meat Fortified with Bee Pollen: Biomedical Research on Laboratory Animals\",\"authors\":\"Maksim Sukhov, Tatiana Giro, Sergey Kozlov, Irina Ziruk\",\"doi\":\"10.21603/2074-9414-2023-4-2476\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Natural food additives can fortify meat products. Bee pollen, also known as beebread or ambrosia, contains amino acids, carbohydrates, vitamins, minerals, enzymes, etc. As a result, it possesses numerous therapeutic and prophylactic properties. Bee pollen has good prospects as a fortifying agent for jerky meat, i.e., lean and dehydrated trimmed meat cut into strips. This study tested dry-cured jerky meat fortified with bee pollen on rats with carbon tetrachloride-induced acute toxic hepatitis. The research featured white non-linear laboratory rats. The control group obtained a standard diet. The experimental rats were induced with liver hepatitis by administering CCl4. On day 2, the experimental group was divided into three subgroups: experimental group I (standard diet + traditional jerky), experimental group II (standard diet + jerky fortified with bee pollen), and experimental group III (standard diet), which served as positive control. The research involved a MicroCC20Vet analyzer for hematological tests and a StatFax 3300 analyzer with Diacon DS diagnostic systems for biochemical tests. The histological analyses relied on the method developed by G.A. Merkulov. The hematological parameters demonstrated no changes. As for the biochemistry, experimental groups I and II developed a protein content increase. On day 14, the concentration of protein and its fractions in experimental group II reached the level of intact animals. In experimental groups II and III, the total protein was significantly higher due to the globulin fraction as a result of inflammatory and destructive processes in the liver. However, the rats had normal live weight gain, and their liver demonstrated no histological deviations. In this preclinical study, bee pollen as part of jerky meat formulation had no negative effect on laboratory rats. 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引用次数: 0
摘要
天然食品添加剂可以强化肉制品。蜂花粉,又称蜂饼或蜂糖,含有氨基酸、碳水化合物、维生素、矿物质、酶等。因此,它具有多种治疗和预防功效。蜂花粉作为肉干(即切成条状的脱水瘦肉)的强化剂具有良好的前景。这项研究在四氯化碳诱发急性中毒性肝炎的大鼠身上测试了添加蜂花粉的干腌牛肉干。 研究对象是白色非线性实验鼠。对照组采用标准饮食。实验组大鼠通过服用四氯化碳诱发肝性肝炎。第 2 天,实验组被分为三个亚组:实验组 I(标准饮食 + 传统肉干)、实验组 II(标准饮食 + 强化蜂花粉肉干)和实验组 III(标准饮食),后者作为阳性对照。研究使用 MicroCC20Vet 分析仪进行血液学检测,使用 StatFax 3300 分析仪和 Diacon DS 诊断系统进行生化检测。组织学分析采用的是 G.A. Merkulov 开发的方法。 血液学参数没有变化。至于生化指标,实验组 I 和 II 的蛋白质含量有所增加。第 14 天,实验组 II 的蛋白质及其组分浓度达到了完整动物的水平。在实验组 II 和 III 中,由于肝脏的炎症和破坏过程,球蛋白部分导致总蛋白质显著增加。不过,大鼠的活体重增加正常,肝脏也没有出现组织学异常。 在这项临床前研究中,蜂花粉作为肉干配方的一部分对实验鼠没有负面影响。蜂花粉还证明了其抗氧化特性。
Raw Cured Poultry Meat Fortified with Bee Pollen: Biomedical Research on Laboratory Animals
Natural food additives can fortify meat products. Bee pollen, also known as beebread or ambrosia, contains amino acids, carbohydrates, vitamins, minerals, enzymes, etc. As a result, it possesses numerous therapeutic and prophylactic properties. Bee pollen has good prospects as a fortifying agent for jerky meat, i.e., lean and dehydrated trimmed meat cut into strips. This study tested dry-cured jerky meat fortified with bee pollen on rats with carbon tetrachloride-induced acute toxic hepatitis. The research featured white non-linear laboratory rats. The control group obtained a standard diet. The experimental rats were induced with liver hepatitis by administering CCl4. On day 2, the experimental group was divided into three subgroups: experimental group I (standard diet + traditional jerky), experimental group II (standard diet + jerky fortified with bee pollen), and experimental group III (standard diet), which served as positive control. The research involved a MicroCC20Vet analyzer for hematological tests and a StatFax 3300 analyzer with Diacon DS diagnostic systems for biochemical tests. The histological analyses relied on the method developed by G.A. Merkulov. The hematological parameters demonstrated no changes. As for the biochemistry, experimental groups I and II developed a protein content increase. On day 14, the concentration of protein and its fractions in experimental group II reached the level of intact animals. In experimental groups II and III, the total protein was significantly higher due to the globulin fraction as a result of inflammatory and destructive processes in the liver. However, the rats had normal live weight gain, and their liver demonstrated no histological deviations. In this preclinical study, bee pollen as part of jerky meat formulation had no negative effect on laboratory rats. Bee pollen also proved its antioxidant properties.