Liu, Shaoshuai
(State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University)
Yan, Wenjuan (Zhejiang BioAsia Biomedical Co., Ltd.) Ma, Chang (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University) Liu, Yajing (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University) Gong, Limin (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University) Levesque, Crystal (Monogastric Nutrition Department of Animal Science, College of Agriculture and Biological Sciences, South Dakota State University) Dong, Bing (State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University) |
1 | Leandro CG, Ribeiro WS, Santos JAD, et al. Moderate physical training attenuates muscle-specific effects on fibre type composition in adult rats submitted to a perinatal maternal low-protein diet. Eur J Nutr 2012;51:807-15. https://doi.org/10.1007/s00394-011-0259-3 DOI |
2 | Staron RS, Malicky ES, Leonardi MJ, Falkel JE, Hagerman FC, Dudley GA. Muscle hypertrophy and fast fiber type conversions in heavy resistance-trained women. Eur J Appl Physiol Occup Physiol 1990;60:71-9. https://doi.org/10.1007/BF00572189 DOI |
3 | Quevedo R, Valencia E, Cuevas G, Ronceros B, Pedreschi F, Bastías JM. Color changes in the surface of fresh cut meat: a fractal kinetic application. Food Res Int 2013;54:1430-6. https://doi.org/10.1016/j.foodres.2013.10.006 DOI |
4 | Wang L, Wang G, Zhang J, et al. Extraction optimization and antioxidant activity of intracellular selenium polysaccharide by Cordyceps sinensis SU-02. Carbohydr Polym 2011;86:1745-50. https://doi.org/10.1016/j.carbpol.2011.07.007 DOI |
5 | Gong M, Zhu Q, Wang T, Wang XL, Ma JX, Zhang WJ. Molecular structure and immunoactivity of the polysaccharide from Cordyceps sinensis (Berk) Sacc. Sheng Wu Hua Hsueh Tsa Chih 1990;6:486-92 (in Chinese). |
6 | Chen WX, Zhang WY, Shen WB, Wang KC. Effects of the acid polysaccharide fraction isolated from a cultivated Cordyceps sinensis on macrophages in vitro. Cell Immunol 2010;262:69-74. https://doi.org/10.1016/j.cellimm.2010.01.001 DOI |
7 | Chen YJ, Shiao MS, Lee SS, Wang SY. Effect of Cordyceps sinensis on the proliferation and differentiation of human leukemic U937 cells. Life Sci 1997;60:2349-59. https://doi.org/10.1016/S0024-3205(97)00291-9 DOI |
8 | Sun YF, Sun Y, Wang Z, et al. Isaria cicadae conidia possess antiproliferative and inducing apoptosis properties in gynaecological carcinoma cells. Mycology 2017;8:327-34. https://doi.org/10.1080/21501203.2017.1386243 DOI |
9 | Zhao LL, Zhi YE, Chen YC, et al. Effect of cordyceps powder feed additive on carcass traits and meat quality in barred rock chicken. J Shanghai Jiaotong Uni (Agricultural Science) 2013; 31:19-22 (in Chinese). https://doi.org/10.3969/J.ISSN.1671-9964.2013.04.004 |
10 | Liu SZ, Li XL, Tu GZ, et al. Effects of waste cultured medium of Isaria cicadae on immune factor and growth performance of broilers. China Poult 2012;34:64-5 (in Chinese). https://doi.org/10.3969/j.issn.1004-6364.2012.09.018 |
11 | Yu S, Chai XY, Fan MZ. Analysis of nutritional and bioactive components of solid-state fermented substrate of isaria cicadae. Food Machinery 2015;31:155-8 (in Chinese). https://doi.org/10.13652/j.issn.1003-5788.2015.01.036 |
12 | Albalasmeh AA, Berhe AA, Ghezzehei TA. A new method for rapid determination of carbohydrate and total carbon concentrations using UV spectrophotometry. Carbohydr Polym 2013;97:253-61. https://doi.org/10.1016/j.carbpol.2013.04.072 DOI |
13 | Van Soest PJ, Robertson JB, Lewis BA. Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. J Dairy Sci 1991;74:3583-97. https://doi.org/10.3168/jds.S0022-0302(91)78551-2 DOI |
14 | Aaslyng MD, Bejerholm C, Ertbjerg P, Bertram HC, Andersen HJ. Cooking loss and juiciness of pork in relation to raw meat quality and cooking procedure. Food Qual Prefer 2003;14:277-88. https://doi.org/10.1016/S0950-3293(02)00086-1 DOI |
15 | Straadt IK, Rasmussen M, Andersen HJ, Bertram HC. Aging-induced changes in microstructure and water distribution in fresh and cooked pork in relation to water-holding capacity and cooking loss-A combined confocal laser scanning microscopy (CLSM) and low-field nuclear magnetic resonance relaxation study. Meat Sci 2007;75:687-95. https://doi.org/10.1016/j.meatsci.2006.09.019 DOI |
16 | Hoffmann E, Thiefes A, Buhrow D, et al. MEK1-dependent delayed expression of fos-related antigen-1 counteracts c-Fos and p65 NF-B-mediated interleukin-8 transcription in response to cytokines or growth factors. J Biol Chem 2005;280:9706-18. https://doi.org/10.1074/jbc.M407071200 DOI |
17 | Zeng Y, Lian S, Li D, et al. Anti-hepatocarcinoma effect of cordycepin against NDEA-induced hepatocellular carcinomas via the PI3K/Akt/mTOR and Nrf2/HO-1/NF-B pathway in mice. Biomed Pharmacother 2017;95:1868-75. https://doi.org/10.1016/j.biopha.2017.09.069 DOI |
18 | Weber A, Wasiliew P, Kracht M. Interleukin-1 (IL-1) pathway. Sci Signal 2010;3:cm1. https://doi.org/10.1126/scisignal.3105 cm1 DOI |
19 | Granowitz EV, Clark BD, Vannier E, Callahan MV, Dinarello CA. Effect of interleukin-1 (IL-1) blockade on cytokine synthesis: I. IL-1 receptor antagonist inhibits IL-1-induced cytokine synthesis and blocks the binding of IL-1 to its type II receptor on human monocytes. Blood 1992;79:2356-63. DOI |
20 | Netea MG, Nold-Petry CA, Nold MF, et al. Differential requirement for the activation of the inflammasome for processing and release of IL-1beta in monocytes and macrophages. Blood 2009;113:2324-35. https://doi.org/10.1182/blood-2008-03-146720 DOI |
21 | Gaestel M, Kotlyarov A, Kracht M. Targeting innate immunity protein kinase signalling in inflammation. Nat Rev Drug Discov 2009;8:480-99. https://doi.org/10.1038/nrd2829 DOI |
22 | Dinarello CA. Immunological and inflammatory functions of the interleukin-1 family. Annu Rev Immunol 2009;27:519-50. https://doi.org/10.1146/annurev.immunol.021908.132612 DOI |
23 | Martinon F, Mayor A, Tschopp J. The inflammasomes: Guardians of the body. Annu Rev Immunol 2009;27:229-65. https://doi.org/10.1146/annurev.immunol.021908.132715 DOI |
24 | Li SP, Zhao KJ, Ji ZN, et al. A polysaccharide isolated from Cordyceps sinensis, a traditional Chinese medicine, protects PC12 cells against hydrogen peroxide-induced injury. Life Sci 2003;73:2503-13. https://doi.org/10.1016/S0024-3205(03)00652-0 DOI |
25 | Qin C, Huang P, Qiu K, et al. Influences of dietary protein sources and crude protein levels on intracellular free amino acid profile in the longissimus dorsi muscle of finishing gilts. J Anim Sci Biotechnol 2015;6:52. https://doi.org/10.1186/s40104-015-0052-x DOI |
26 | Wang H, Liu YM, Qi ZM, et al. An overview on natural polysaccharides with antioxidant properties. Curr Med Chem 2013;20:2899-913. https://doi.org/10.2174/09298673113202 30006 DOI |
27 | Wang Y, Yin H, Lv X, Wang Y, Gao H, Wang M. Protection of chronic renal failure by a polysaccharide from Cordyceps sinensis. Fitoterapia 2010;81:397-402. https://doi.org/10.1016/j.fitote.2009.11.008 DOI |
28 | Shen L, Lei H, Zhang S, et al. The comparison of energy metabolism and meat quality among three pig breeds. Anim Sci J 2014;85:770-9. https://doi.org/10.1111/asj.12207 DOI |
29 | Cunningham KG, Hutchinson SA, Manson W, Spring FS. Cordycepin, a metabolic product from cultures of Cordyceps militaris (Linn.) link. Part 1. Isolation and characterisation. J Chem Soc 1951;2:2299-300. https://doi.org/10.1039/JR9510002299 |
30 | Zhang SS, Zhang DS, Zhu TJ, Chen XY. A pharmacological analysis of the amino acid components of Cordyceps sinensis Sacc. Acta Pharm Sin B 1991;26:326-30 (in Chinese). |
31 | Wang J, Zhang DM, Jia JF, et al. Cyclodepsipeptides from the ascocarps and insect-body portions of fungus Cordyceps cicadae. Fitoterapia 2014;97:23-7. https://doi.org/10.1016/j.fitote.2014.05.010 DOI |
32 | Won KJ, Lee SC, Lee CK, et al. Cordycepin attenuates neointimal formation by inhibiting reactive oxygen species-mediated responses in vascular smooth muscle cells in rats. J Pharmacol Sci 2009;109:403-12. https://doi.org/10.1254/jphs.08308FP DOI |
33 | Ramesh T, Yoo SK, Kim SW, et al. Cordycepin (3'-deoxyadenosine) attenuates age-related oxidative stress and ameliorates antioxidant capacity in rats. Exp Gerontol 2012;47:979-87. https://doi.org/10.1016/j.exger.2012.09.003 DOI |
34 | He L, Shi W, Liu X, Zhao X, Zhang Z. Anticancer action and mechanism of ergosterol peroxide from Paecilomyces cicadae fermentation broth. Int J Mol Sci 2018;19:3935. https://doi.org/10.3390/ijms19123935 DOI |
35 | Ukai S, Kiho T, Hara C, et al. Polysaccharides in fungi. XIII. Antitumor activity of various polysaccharides isolated from Dictyophora indusiata, Ganoderma japonicum, Cordyceps cicadae, Auricularia auricula-judae, and Auricularia species. Chem Pharm Bull 1983;31:741-4. https://doi.org/10.1248/cpb.31.741 DOI |
36 | Weng SC, Chou CJ, Lin LC, Tsai WJ, Kuo YC. Immunomodulatory functions of extracts from the Chinese medicinal fungus Cordyceps cicadae. J Ethnopharmacol 2002;83:79-85. https://doi.org/10.1016/S0378-8741(02)00212-X DOI |
37 | Olatunji OJ, Feng Y, Olatunji OO, et al. Polysaccharides purified from Cordyceps cicadae protects PC12 cells against glutamate-induced oxidative damage. Carbohydr Polym 2016;153:187-95. https://doi.org/10.1016/j.carbpol.2016.06.108 DOI |
38 | Zeng WB, Yu H, Ge F, et al. Distribution of nucleosides in populations of Cordyceps cicadae. Molecules 2014;19:6123-41. https://doi.org/10.3390/molecules19056123 DOI |
39 | Cheng Z, He W, Zhou X, et al. Cordycepin protects against cerebral ischemia/reperfusion injury in vivo and in vitro. Eur J Pharmacol 2011;664:20-8. https://doi.org/10.1016/j.ejphar.2011.04.052 DOI |
40 | Miyazaki T, Yadomae T, Terui T, Yamada H, Kikuchi T. Studies on fungal polysaccharide XVII. A new glucuronan "protuberic acid" produced by a fungus Kobayashi Nipponica. Biochim Biophys Acta Gen Subj 1975;385:345-53. https://doi.org/10.1016/0304-4165(75)90363-3 DOI |
41 | Yamada H, Kawaguchi N, Ohmori T, Takeshita Y, Taneya S, Miyazaki T. Structure and antitumor activity of an alkali-soluble polysaccharide from Cordyceps ophioglossoides. Carbohydr Res 1984;125:107-15. https://doi.org/10.1016/0008-6215(84)85146-0 DOI |
42 | Jiang ZY, Jiang SQ, Lin YC, Xi PB, Yu DQ, Wu TX. Effects of soybean isoflavone on growth performance, meat quality, and antioxidation in male broilers. Poult Sci 2007;86:1356-62. https://doi.org/10.1093/ps/86.7.1356 DOI |
43 | Zhan XA, Wang M, Zhao RQ, Li WF, Xu ZR. Effects of different selenium source on selenium distribution, loin quality and antioxidant status in finishing pigs. Anim Feed Sci Technol 2007;132:202-11. https://doi.org/10.1016/j.anifeedsci.2006.03.020 DOI |
44 | Monahan FJ, Gray JI, Asghar A, et al. Influence of diet on lipid oxidation and membrane structure in porcine muscle microsomes. J Agric Food Chem 1994;42:59-63. https://doi.org/10.1021/jf00037a009 DOI |
45 | Won KJ, Lee SC, Lee CK, et al. Cordycepin attenuates neointimal formation by inhibiting reactive oxygen species-mediated responses in vascular smooth muscle cells in rats. J Pharmacol Sci 2009;109:403-12. https://doi.org/10.1254/jphs.08308FP DOI |
46 | Zhang C, Luo J, Yu B, et al. Dietary resveratrol supplementation improves meat quality of finishing pigs through changing muscle fiber characteristics and antioxidative status. Meat Sci 2015;102:15-21. https://doi.org/10.1016/j.meatsci.2014.11.014 DOI |