馬齒苋水提物(wù)對鯉生(sheng)長(zhang)性能(néng)、血清(qing)、肝髒咊(he)黏液免疫及(ji)炎症因子(zi)的(de)影響

AQUEOUS EXTRACT OF PURSANE (PORTULACA OLERACEA) ON GROWTH PERFORMANCE, SERUM, LIVER AND MUCUS IMMUNITY, AND INFLAMMATORY FACTOR GENE EXPRESSION IN COMMON CARP (CYPRINUS CARPIO)

  • 摘要: 本(ben)實驗(yàn)旨在(zai)探究飼料中(zhong)添加(jia)不同水平馬齒苋水提物(wù)(Aqueous Extract of Portulaca oleracea, AEP)對鯉生(sheng)長(zhang)性能(néng)、血清(qing)、肝髒咊(he)黏液免疫及(ji)免疫器(qi)官炎症因子(zi)基因表達的(de)影響。選取240尾健康且體(ti)重(zhong)相近(32.00±0.50) g的(de)鯉幼魚, 随機(jī)分(fēn)爲(wei)4箇(ge)組, 每組3箇(ge)重(zhong)複, 每箇(ge)重(zhong)複20尾, 對照組飼喂不加(jia)AEP的(de)基礎飼料、實驗(yàn)組飼喂在(zai)基礎飼料中(zhong)分(fēn)别添加(jia)0.25%(AEP0.25%組)、0.50%(AEP0.50%組)咊(he)1.00%(AEP1.00%組) AEP的(de)飼料, 實驗(yàn)周期爲(wei)8周。結果表明: (1)與對照組相比, 實驗(yàn)組鯉的(de)終末體(ti)重(zhong)(FBW)、增重(zhong)率(WGR)、特定生(sheng)長(zhang)率(SGR)、飼料係(xi)數(shu)(FCR)咊(he)攝食率(FR)均無顯著影響(P> 0.05); 其髒體(ti)比(VSI)均顯著降低, 肥滿度(CF)則均顯著升高(gao)(P<0.05)。(2)與對照組相比, AEP0.25%組鯉血清(qing)中(zhong)酸性磷酸酶(ACP)活性顯著增強(P<0.05), 而髓過(guo)氧化物(wù)酶(MPO)活性顯著降低(P<0.05); AEP0.50%組血清(qing)中(zhong)免疫球蛋白(Ig)含量顯著升高(gao)(P<0.05)。(3)與對照相比, AEP0.25%組咊(he)AEP1.00%組鯉肝髒中(zhong)谷丙轉氨酶(GPT)活性顯著降低(P<0.05); AEP1.00%組Ig含量咊(he)堿性磷酸酶(AKP)的(de)活性均顯著升高(gao)(P<0.05)。(4)與對照組相比, AEP0.50%組鯉黏液中(zhong)AKP活性顯著增強(P<0.05), 過(guo)氧化物(wù)酶(POD)咊(he)蛋白酶活性均無顯著影響(P>0.05)。(5)在(zai)脾髒組織中(zhong), 與對照組相比, AEP0.25%組咊(he)AEP0.50%組TNF-α咊(he)TGF-β表達水平均顯著下調(P<0.05); AEP1.00%組的(de)TNF-α表達水平顯著低于(yu)對照組(P<0.05); 在(zai)腎髒組織中(zhong), 與對照組相比, 各實驗(yàn)組IL-1β表達水平均顯著下調(P<0.05); AEP0.50%組咊(he)AEP1.00%組IL-10表達水平顯著下調。綜上所述, 飼料中(zhong)添加(jia)适量馬齒苋水提物(wù)在(zai)不影響鯉生(sheng)長(zhang)性能(néng)的(de)情況下, 能(néng)夠增強其血清(qing)、肝髒及(ji)黏液免疫功能(néng), 調控免疫器(qi)官炎症因子(zi)的(de)基因表達, 進(jin)而可(kě)能(néng)對機(jī)體(ti)的(de)免疫應答(dá)過(guo)程(cheng)髮(fa)揮積極作(zuò)用(yong)。

     

    Abstract: This experiment was conducted to investigate the effects of dietary supplementation with Aqueous Extract of Portulaca oleracea (AEP) on growth performance, serum, liver and mucus immunity, and inflammatory factor gene expression in immune organs of common carp (Cyprinus carpio). A total of 240 juvenile carp (32.00±0.50) g were randomly divided into four dietary groups with three replicates in each group and 20 carps in each replicate. The control group was fed with basal diet without AEP, and the experimental groups were fed with basal diet supplemented with 0.25%, 0.50% and 1.00% AEP for 8 weeks, respectively. Results demonstrated the following key findings: 1) Compared with the control group, the final body weight (FBW), weight gain rate (WGR), specific growth rate (SGR), feed coefficient (FCR), and feeding rate (FR) were not significantly affected (P>0.05). However, the viscerosomatic index (VSI) was significantly decreased and the condition factor (CF) was significantly increased (P<0.05). 2) The AEP 0.25% group manifested distinct serum profile alterations, with acid phosphatase (ACP) activity significantly elevated (P<0.05) and myeloperoxidase (MPO) activity markedly reduced (P<0.05) compared to controls. Serum immunoglobulin (Ig) levels showed a significant increase in the 0.50% AEP treatment group (P<0.05). 3) Liver analysis revealed significant decreases in alanine aminotransferase (GPT) activity for both 0.25% and 1.00% AEP groups compared to controls (P<0.05). The content of Ig and the activity of alkaline phosphatase (AKP) in 1.00% AEP group were significantly increased (P<0.05). 4) Compared with the control group, AKP activity in the mucus of carp in the 0.50% AEP group was significantly increased (P<0.05), with no change in Peroxidase (POD) or protease activities (P>0.05). 5) The mRNA expression analysis revealed that TNF-α and TGF-β levels in spleen tissue were downregulated in the 0.25% and 0.50% AEP groups (P<0.05), and TNF-α was also reduced in the 1.00% AEP group (P<0.05). In kidney tissue, IL-1β expression was significantly down-regulated across all AEP treatments, while IL-10 was significantly reduced in 0.50% and 1.00% AEP groups (P<0.05). In conclusion, dietary AEP supplementation enhance the immune function in serum, liver, and mucus of common carp without affecting growth performance. It also modulates the gene expression of inflammatory factors in immune organs, suggesting a potentially beneficial role in immune response process of the organism.

     

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