PLANT BIOLOGY
ANIMAL BIOLOGY
SUBSCRIPTION
E-SUBSCRIPTION
 
MAP
MAIN PAGE

 

 

 

 

doi: 10.15389/agrobiology.2025.2.220eng

UDC: 636.2:636.018:636.084

Acknowledgements:
Supported by the RSF project No. 22-76-10008

 

USE OF PHYTOCHEMICALS IN CATTLE FEEDING (review)

D.E. Shoshin, K.N. Atlanderova

Federal Research Centre of Biological Systems and Agrotechnologies RAS, 29, ul. 9 Yanvarya, Orenburg, 460000, e-mail daniilshoshin@mail.ru (✉ corresponding author), atlander-kn@mail.ru

ORCID:
Shoshin D.E. orcid.org/0000-0003-3086-681X
Atlanderova K.N. orcid.org/0000-0003-3977-4831

Final revision received March 04, 2024

Accepted April 27, 2024

The use of feed antibiotics is the most common way to stimulate the growth and increase productivity of animals used for food production. However, the irrational use of antibacterial drugs in the feed industry is becoming a key reason for the persistence of residual amounts of antibiotics in animal products and the development of antibiotic resistance in pathogenic microorganisms. The problem of antibiotic resistance is one of the main ones in the world, since the emergence of bacterial resistance mechanisms to antibiotic compounds leads to a decrease in the effectiveness of treatment of infectious diseases in both animals and humans who consume animal products (H. Hao, et al., 2014). The use of phytochemicals (phytobiotics, PB), the secondary plant metabolites terpenoids, alkaloids, and phenolic compounds (A. Bernhoft, 2010) in feeding ruminants, especially cattle is an alternative to antibiotic growth stimulants (S. Reddy et al., 2022) and s the taste and attractiveness of the diet (S.F. Sukhanova et al., 2015). PB effectively affect the cell membranes of pathogenic microorganisms due to lipophilicity and small size of active molecules (S. Burt, 2004). This ability leads to disorganization of the cellular structures of prokaryotes and inhibition of quorum sensing processes, which prevents the spread of infections and improves the overall microbiota of the intestinal tract (A. Ultee et al., 2000; K.S. Kondrashova et al., 2020). The purpose of this work is analysis of the global practice of using phytobiotic drugs in cattle feeding and to summarize the metabolic effects they mediate in connection with the chemical structure of their constituent molecules. According to research data (M.J. Groot et al., 2011; M.E.N. Soroor et al., 2015), PB contribute to a decrease in the number of methanogenic and ammonia-producing bacteria in the rumen, resulting in a decrease in greenhouse gas emissions. PB has a positive effect on increasing the total bacterial mass in the rumen (M. Wanapat et al., 2008). A richer and more diverse microbiome improves the fermentation of feed, contributing to the efficient extraction of nutrients. This leads to a more complete breakdown of fiber and other complex carbohydrates contained in the diet, and, as a result, increases the digestibility and digestibility of nutrients (M. Tajodini et al., 2014), growth rates and immune status of animals (A. Rahal et al., 2012). Some secondary metabolites can regulate the hormonal production of the ovaries (R. Kumar et al., 2013), increase milk production, prevent udder infection (S. Kumar et al., 2008), and improve the reproductive performance of cows (R. Kumar et al., 2013). Moreover, phytochemicals have antiinflammatory properties (F. Muanda et al., 2011) and antioxidant properties (C.A. Rice-Evans et al., 2003). They can inhibit peroxidation of membrane lipids, chelate metals and stimulate the production of antioxidant enzymes (S. Calsamiglia et al., 2007), contribute to the fight against free radicals and oxidative stress, which can negatively affect the health and productivity of animals. However, the efficacy and safety of the use of PB depend on many factors (D. E. Cross et al., 2007; Y. Yang et al., 2009), which requires a more detailed and comprehensive study of such growth metabolites.

Keywords: cattle, feeding, phytochemicals, phytobiotics, antibiotic resistance, microbiocenosis.

 

REFERENCES

  1. Arkhipov A.V., Toporova L.V. Glavnyy zootekhnik, 2013, 9: 3-12 (in Russ.).
  2. Bukharova S.V. Bukharova T.V., Vagapova O.A. Sbornik trudov Mezhdunarodnoy nauchno-prakticheskoy onlayn konferentsii «Prioritetnye napravleniya nauchno-tekhnologicheskogo razvitiya agropromyshlennogo kompleksa» [Proc. Int. Conf. «Priority areas of scientific and technological development of the agro-industrial complex»]. Novosibirsk, 2020: 30-33 (in Russ.).
  3. Anadón A. WS14 The EU ban of antibiotics as feed additives: alternatives and consumer safety. Journal of Veterinary Pharmacology and Therapeutics, 2006, 29(s1): 41-44 CrossRef
  4. Wegener H.C. Antibiotics in animal feed and their role in resistance development. Current Opinion in Microbiology, 2003, 6(5): 439-445 CrossRef
  5. Hao H., Cheng G., Iqbal Z., Ai X., Hussain H.I., Huang L., Dai M., Wang Y., Liu Z., Yuan Z. Benefits and risks of antimicrobial use in food-producing animals. Frontiers in Microbiology, 2014, 5: 288 CrossRef
  6. Gadde U., Kim W.H., Oh S.T., Lillehoj H.S. Alternatives to antibiotics for maximizing growth performance and feed efficiency in poultry: a review. Animal Health Research Reviews, 2017, 18(1): 26-45 CrossRef
  7. Reddy S., Barathe P., Kaur K., Anand U., Shriram V., Kumar V. Antimicrobial resistance and medicinal plant products as potential alternatives to antibiotics in animal husbandry. In: Antimicrobial resistance: underlying mechanisms and therapeutic approaches. V. Kumar, V. Shriram, A. Paul, M. Thakur (eds.). Springer, Singapore, 2022: 357-384 CrossRef
  8. Petrusha Yu.K., Lebedev S.V., Grechkina V.V. Zhivotnovodstvo i kormoproizvodstvo, 2022, 105(1): 103-118 CrossRef (in Russ.).
  9. Popova G.M., Nurzhanov B.S., Duskaev G.K. Zhivotnovodstvo i kormoproizvodstvo, 2023, 106(2): 152-175 CrossRef (in Russ.).
  10. Duskaev G.K., Klimova T.A. Zhivotnovodstvo i kormoproizvodstvo, 2022, 105(3): 137-152 CrossRef (in Russ.).
  11. Bagno O.A., Prokhorov O.N., Shevchenko S.A., Shevchenko A.I., Dyadichkina T.V. Use of phytobioticts in farm animal feeding (review). Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2018, 53(4): 687-669 CrossRef
  12. Dias D.A., Urban S., Roessner U. A historical overview of natural products in drug discovery. Metabolites, 2012, 2(2): 303-336 CrossRef
  13. Lentochkin A.M. Lekarstvennye rasteniya v veterinarii: uch. pos. k prakt. zanyatiyam i dlya samostoyat. raboty studentov, obuchayushchikhsya po spetsial’nosti «Veterinariya» [Medicinal plants in veterinary science: A manual for practical classes and independent work of students studying in the specialty "Veterinary science"].Izhevsk, 2022 (in Russ.).
  14. Petrovska B.B. Historical review of medicinal plants’ usage. Pharmacognosy Reviews, 2012, 6(11): 1-5 CrossRef
  15. Seth S.D., Sharma B. Medicinal plants in India. Indian Journal of Medical Research, 2004, 120(1): 9.
  16. Tang W., Eisenbrand G. Chinese drugs of plant origin: chemistry, pharmacology, and use in traditional and modern medicine. Springer Science & Business Media, 2013.
  17. Velu G., Palanichamy V., Rajan, A.P. Phytochemical and pharmacological importance of plant secondary metabolites in modern medicine. In: Bioorganic phase in natural food: an overview. S. Roopan, G. Madhumitha (eds.). Springer, Cham, 2018: 135-156 CrossRef
  18. Bhatla S.C., Lal A.M. Secondary metabolites. In: Plant physiology, development and metabolism. S.C. Bhatla, A.M. Lal (eds.). Springer, Singapore, 2018: 1099-1166 CrossRef
  19. Thrane U. Development in the taxonomy of Fusarium species based on secondary metabolites. In: Fusarium: Paul E. Nelson memorial symposium. B.A. Summerell (ed.). APS Press, St. Paul, Minnesota, 2001: 29-49.
  20. Bernhoft A. A brief review on bioactive compounds in plants. In: Bioactive compounds in plants-benefits and risks for man and animals. A. Bernhoft (ed.). The Norwegian Academy of Science and Letters, Oslo, 2010: 11-17.
  21. Makkar H.P.S., Francis G., Becker K. Bioactivity of phytochemicals in some lesser-known plants and their effects and potential applications in livestock and aquaculture production systems. Animal, 2007, 1(9): 1371-1391 CrossRef
  22. Ansari J.Z., Haq A., ul Yousaf M., Ahmad T., Khan S. Evaluation of different medicinal plants as growth promoters for broiler chicks. Sarhad Journal of Agriculture, 2008, 24(2): 323-329.
  23. Jamroz D., Orda J., Kamel C., Wiliczkiewicz A., Wertelecki T., Skorupińska J. The influence of phytogenic extracts on performance, nutrient digestibility, carcass characteristics, and gut microbial status in broiler chickens. Journal of Animal and Feed Sciences, 2003, 12(3): 583-596 CrossRef
  24. Vidanarachchi J.K., Elangovan A.V., Mikkelsen L.L., Choct M., Iji P.A. Effect of some plant extracts on growth performance, intestinal morphology, microflora composition and activity in broiler chickens. Animal Production Science, 2010, 50(9): 880-889 CrossRef
  25. O’Bryan C.A., Pendleton S.J., Crandall P.G., Ricke S.C. Potential of plant essential oils and their components in animal agriculture — in vitro studies on antibacterial mode of action. Frontiers in Veterinary Science, 2015, 2: 35 CrossRef
  26. Diniz do Nascimento L., Barbosa de Moraes A.A., Santana da Costa K., Pereira Galúcio J.M., Taube P.S., Leal Costa C.M., Neves Cruz J., Helena de Aguiar Andrade E., Guerreiro de Faria L.J. Bioactive natural compounds and antioxidant activity of essential oils from spice plants: new findings and potential applications. Biomolecules, 2020, 10(7): 988 CrossRef
  27. Franz C., Baser K.H.C., Windisch W. Essential oils and aromatic plants in animal feeding — a European perspective. A review. Flavour and Fragrance Journal, 2010, 25(5): 327-340 CrossRef
  28. Sethiya N.K. Review on natural growth promoters available for improving gut health of poultry: an alternative to antibiotic growth promoters. Asian Journal of Poultry Science, 2016, 10(1): 1-29 CrossRef
  29. Lillehoj H., Liu Y., Calsamiglia S., Fernandez-Miyakawa M.E., Chi F., Cravens R.L., Gay C.G. Phytochemicals as antibiotic alternatives to promote growth and enhance host health. Veterinary Research, 2018, 49(1): 76 CrossRef
  30. Faniyi T.O., Adewumi M.K., Prates Ê.R., Ayangbenro A.S. Effect of herbs and spices (plant extracts) on rumen microbial activities: a review. Pubvet, 2016, 10(6): 477-486 CrossRef
  31. Dewick P.M. Medicinal natural products: a biosynthetic approach. New York: Jonh Wiley & Sons Ltd, 2002.
  32. Giweli A.A., Džamić A.M., Soković M., Ristić M., Janaćković P., Marin P. The chemical composition, antimicrobial and antioxidant activities of the essential oil of Salvia fruticosa growing wild in Libya. Archives of Biological Sciences, 2013, 65(1): 321-329.
  33. Bohlmann J., Keeling C.I. Terpenoid biomaterials. The Plant Journal, 2008, 54(4): 656-669 CrossRef
  34. Plant secondary metabolites: occurrence, structure and role in the human diet. A. Crozier, M.N. Clifford, H. Ashihara (eds.) Blackwell-Publishers, 2006 CrossRef
  35. Rohmer M., Knani M., Simonin P., Sutter B., Sahm H. Isoprenoid biosynthesis in bacteria: a novel pathway for the early steps leading to isopentenyl diphosphate. Biochemical Journal, 1993, 295(2): 517-524 CrossRef
  36. Eisenreich W., Bacher A., Arigoni D., Rohdich F., Biosynthesis of isoprenoids via the non-mevalonate pathway. Cellular and Molecular Life Sciences CMLS, 2004; 61: 1401-1426 CrossRef
  37. Ershov Y., Gantt R.R., Cunningham F.X., Gantt E. Isopentenyl diphosphate isomerase deficiency in Synechocystis sp. strain PCC6803. FEBS Letters, 2000: 473(3): 337-340 CrossRef
  38. da S. Agostini-Costa T., Vieira R.F., Bizzo H.R., Silveira D., Gimenes M.A. Secondary metabolites. In: Chromatography and its applications. S. Dhanarasu (ed.). IntechOpen, 2012 CrossRef
  39. Turlings T.C.J., Loughrin J.H., McCall P.J., Röse U.S.R., Lewis W.J., Tumlinson J.H. How caterpillardamaged plants protect themselves by attracting parasitic wasps. Proceeding of the National Academy of Sciences of the USA, 1995, 92: 4169-4174 CrossRef
  40. Ensley S.M. Pyrethrins and pyrethroids. In: Veterinary toxicology. Academic Press, 2018: 512-520 CrossRef
  41. Chaturvedi D. Sesquiterpene lactones: structural diversity and their biological activities. In: Opportunity, challanges and scope of natural products in medicinal chemistry. D. Chaturvedi (ed.). Research Signpost, Trivandrum, 2011: 313-334.
  42. Kumar R., Kumar R., Sharma N., Khurana N. Ameliorative effect of myrcene in mouse model of Alzheimer's disease. European Journal of Pharmacology, 2021, 911: 174529 CrossRef
  43. Mączka W., Wińska K., Grabarczyk M. One hundred faces of geraniol. Molecules, 2020, 25(14): 3303 CrossRef
  44. Ilc T., Parage C., Boachon B., Navrot N., Werck-Reichhart D. Monoterpenol oxidative metabolism: role in plant adaptation and potential applications. Frontiers in Plant Science, 2016, 7: 509 CrossRef
  45. Bazemore R., Rouseff R., Naim M. Linalool in orange juice: origin and thermal stability. Journal of Agricultural and Food Chemistry, 2003, 51(1): 196-199 CrossRef
  46. Özek T., Tabanca N., Demirci F., Wedge D.E., Başer K.H.C. Enantiomeric distribution of some linalool containing essential oils and their biological activities. Rec. Nat. Prod., 2010, 4(4): 180-192.
  47. Báez D., Pino J.A., Morales D. Floral scent composition in Hedychium coronarium J. Koenig analyzed by SPME. Journal of Essential Oil Research, 2011, 23(3): 64-67 CrossRef
  48. Gochev V., Wlcek K., Buchbauer G., Stoyanova A., Dobreva A., Schmidt E., Jirovetz L. Comparative evaluation of antimicrobial activity and composition of rose oils from various geographic origins, in particular Bulgarian rose oil. Natural Product Communications, 2008, 3(7): 1934578X0800300706 CrossRef
  49. Sharopov F.S., Zhang H., Setzer W.N. Composition of geranium (Pelargonium graveolens) essential oil from Tajikistan. American Journal of Essential Oils and Natural Products, 2014, 2(2): 13-16.
  50. Ganjewala D. Cymbopogon essential oils: chemical compositions and bioactivities. International Journal of Essential Oil Therapeutics, 2009, 3(2-3): 56-65.
  51. Thorsell W., Mikiver A., Malander I., Tunon H. Efficacy of plant extracts and oils as mosquito repellents. Phytomedicine, 1998, 5(4): 311-323 CrossRef
  52. Kim Y.W., Kim M.J., Chung B.Y., Bang D.Y., Lim S.K., Choi S.M., Lim D.S., Cho M.C., Yoon K., Kim H.S., Kim K.B., Kim Y.S., Kwack S.J., Lee B.M. Safety evaluation and risk assessment of d-limonene. Journal of Toxicology and Environmental Health, Part B, 2013, 16(1): 17-38 CrossRef
  53. Zhao H., Ren S., Yang H., Tang S., Guo C., Liu M., Tao Q., Ming T., Xu H. Peppermint essential oil: Its phytochemistry, biological activity, pharmacological effect and application. Biomedicine & Pharmacotherapy, 2022, 154: 113559 CrossRef
  54. Hamidpour R., Hamidpour S., Hamidpour M., Shahlari M. Camphor (Cinnamomum camphora), a traditional remedy with the history of treating several diseases. International Journal of Case Reports and Clinical Images, 2013, 4(2): 86-89.
  55. Nadda R.K., Ali A., Goyal R.C., Khosla P.K., Goyal R. Aucklandia costus (syn. Saussurea costus): ethnopharmacology of an endangered medicinal plant of the Himalayan region. Journal of Ethnopharmacology, 2020, 263: 113199 CrossRef
  56. Van Steveninck R.F.M., Van Steveninck M.E. Abscisic acid and membrane transport. In: Abscisic acid. F.T. Addicott (ed.). Praeger Publishers, New York, 1983: 171-235.
  57. Berli F.J., Moreno D., Piccolo P., Hespanhol-Viana L., Silva M.F., Bressan-Smith R., Bottini R. Abscisic acid is involved in the response of grape (Vitis vinifera L.) cv. Malbec leaf tissues to ultraviolet-B radiation by enhancing ultraviolet-absorbing compounds, antioxidant enzymes and membrane sterols. Plant Cell & Environment, 2010, 33(1): 1-10 CrossRef
  58. Gudkova E., Le Ngok N., Ustinova M. Mutual influence of biologically active compounds in medical plants composition. Proc. 1st International Symposium Innovations in Life Sciences (ISILS 2019). Atlantis Press, 2019: 220-225 CrossRef
  59. Evstratova R.I., Kabanov V.S., Krylova I.L., Prokosheva L.I. Content of essential oil and of ledol in leaves of marsh rosemary (Ledum palustre L.) during different phases of vegetation. Pharmaceutical Chemistry Journal, 1978, 12(11): 1468-1473 CrossRef
  60. Njoroge S.M., Koaze H., Karanja P.N., Sawamura M. Essential oil constituents of three varieties of Kenyan sweet oranges (Citrus sinensis). Flavour and Fragrance Journal, 2005, 20(1): 80-85 CrossRef
  61. Riesmeier M., Mattonai M., Wong S.S., Veall M.A., Betts J., Johnston M., Devièse T. Molecular profiling of Peru Balsam reveals active ingredients responsible for its pharmaceutical properties. Natural Product Research, 2021, 35(23): 5311-5316 CrossRef
  62. Tundis R., Loizzo M.R., Menichini F., Statti G.A., Menichini F. Biological and pharmacological activities of iridoids: recent developments. Mini-Reviews in Medicinal Chemistry, 2008, 8(4): 399-420 CrossRef
  63. Moujir L., Callies O., Sousa P.M., Sharopov F., Seca A.M. Applications of sesquiterpene lactones: a review of some potential success cases. Applied Sciences, 2020, 10(9): 3001 CrossRef
  64. Zeng X., Guo F., Ouyang D. A review of the pharmacology and toxicology of aucubin. Fitoterapia, 2020, 140: 104443 CrossRef
  65. Lone S.H., Bhat K.A., Khuroo M.A. Arglabin: from isolation to antitumor evaluation. Chemico-Biological Interactions, 2015, 240: 180-198 CrossRef
  66. Knoff D.B. Regulatory phosphorylation of chloroplast antenna proteins. Trends Biochemical Sciences, 1991, 16: 82-83 CrossRef
  67. Davies P.J. The plant hormone concept: concentration, sensitivity and transport. In: Plant hormones: physiology, biochemistry and molecular biology. P.J. Davies (ed.). Dordrecht: Springer Netherlands, 1995: 13-38 CrossRef
  68. Bishnoi N.R., Krishnamoorthy H.N. Effect of waterlogging and gibberellic acid on leaf gas exchange in peanut (Arachis hypogaea L.). Journal of Plant Physiology, 1992, 139(4): 503-505 CrossRef
  69. Gupta V.N., Datta S.K. Influence of gibberellic acid on growth and flowering in chrysanthemum (Chrysanthemum morifolium Rahmat) cv. Jayanti. Indian Journal of Plant Physiology, 2001, 6: 420-422.
  70. Ouzouidou G., Llias I., Hormone induced protection of sunflower photosynthetic apparatus against copper toxicity. Plant Biology, 2005, 49: 223-228 CrossRef
  71. Croteau R., Kutchan T.M., Lewis N.G. Natural products (secondary metabolites). In: Biochemistry and molecular biology of plants /B. Buchanan, W. Gruissem, R. Jones (eds.). American Society of Plant Biologists, Rockville, 2000: 1250-1319.
  72. Mikson D.S., Roshchin V.I. The Siberian larch needle group composition and acids at various vegetation periods. Russian Journal of Bioorganic Chemistry, 2020, 46: 1396-1402 CrossRef
  73. D’Ambrosio D.N., Clugston R.D., Blaner W.S. Vitamin A metabolism: an update. Nutrients, 2011, 3(1): 63-103 CrossRef
  74. Chatsudthipong V., Muanprasat C. Stevioside and related compounds: therapeutic benefits beyond sweetness. Pharmacology & therapeutics, 2009, 121(1): 41-54 CrossRef
  75. Abe I. Enzymatic synthesis of cyclic triterpenes. Natural Product Reports, 2007, 24(6): 1311-1331 CrossRef
  76. Tantillo D.J. Biosynthesis via carbocations: theoretical studies on terpene formation. Natural Product Reports, 2011, 28(6): 1035-1053 CrossRef
  77. Augustin J.M., Kuzina V., Andersen S.B., Bak S. Molecular activities, biosynthesis and evolution of triterpenoid saponins. Phytochemistry, 2011, 72(6): 435-457 CrossRef
  78. Birnbaum S.S.L., Abbot P. Insect adaptations toward plant toxins in milkweed — herbivores systems — a review. Entomologia Experimentalis et Applicata, 2018, 166(5): 357-366 CrossRef
  79. Sláma K. Animal hormone and antihormones in plants. Biochemie und Physiologie der Pflanzen, 1980, 175: 177-193 CrossRef
  80. Mordue A.J. Present concepts of the mode of action of azadirachtin from neem. In: Neem: Today and in the new millennium. O. Koul, S. Wahab (eds.). Springer Netherlands, Dordrecht, 2004: 294-242 CrossRef
  81. Britton G. Structure and properties of carotenoids in relation to function. The FASEB Journal, 1995, 9(15): 1551-1558 CrossRef
  82. Clinton S.K. Lycopene: chemistry, biology, and implications for human health and disease. Nutrition Reviews, 1998, 56(2): 35-51 CrossRef
  83. Zeb A., Mehmood S. Carotenoids contents from various sources and their potential health applications. Pakistan Journal of Nutrition, 2004, 3(3): 199-204 CrossRef
  84. Babenko L.M., Smirnov O.E., Romanenko K.O., Trunova O.K., Kosakivska I.V. Phenolic compounds in plants: biogenesis and functions. The Ukrainian Biochemical Journal, 2019, 91(3): 5-18 CrossRef
  85. Chalker-Scott L., Fuchigami L.H. The role of phenolic compounds in plant stress responses. In: Low temperature stress physiology in crops. P.H. Li (ed.). CRC Press, Boca Raton, Florida, 2018: 67-80.
  86. Saltveit M.E. Synthesis and metabolism of phenolic compounds. In: Fruit and vegetable phytochemicals: chemistry and human health, 2nd edition. E.M. Yahia (ed.). John Wiley & Sons, 2017: 115-124 CrossRef
  87. Tsimogiannis D., Oreopoulou V. Classification of phenolic compounds in plants. In: Polyphenols in plants (second edition). R.R. Watson (ed.). Academic Press, 2019: 263-284 CrossRef
  88. Al-Katib S., Al-Khashab E., Kalo M., Hamdoon A. The antioxidant effects of flavonoids and non-flavonoid part extracted from ginger (Zingiber officinale) roots. Rafidain Journal of Science, 2009, 20(3): 18-31 CrossRef
  89. Aherne S.A., O’Brien N.M. Dietary flavonols: chemistry, food content, and metabolism. Nutrition, 2002, 18(1): 75-81 CrossRef
  90. Jiang N., Doseff A.I., Grotewold E. Flavones: from biosynthesis to health benefits. Plants, 2016, 5(2): 27 CrossRef
  91. Ho S.-C., Kuo C.T. Hesperidin, nobiletin, and tangeretin are collectively responsible for the anti-neuroinflammatory capacity of tangerine peel (Citrireticulatae pericarpium). Food and Chemical Toxicology, 2014, 71: 176-182 CrossRef
  92. Chen Z., Kong S., Song F., Li L., Jiang H. Pharmacokinetic study of luteolin, apigenin, chrysoeriol and diosmetin after oral administration of Flos Chrysanthemi extract in rats. Fitoterapia, 2012, 83(8): 1616-1622 CrossRef
  93. Cui L., Liu Y., Liu T., Yuan Y., Yue T., Cai R., Wang Z. Extraction of epigallocatechin gallate and epicatechin gallate from tea leaves using β‐cyclodextrin. Journal of Food Science, 2017, 82(2): 394-400 CrossRef
  94. Khoo H.E., Azlan A., Tang S.T., Lim S.M. Anthocyanidins and anthocyanins: colored pigments as food, pharmaceutical ingredients, and the potential health benefits. Food & Nutrition Research, 2017, 61(1): 1361779 CrossRef
  95. Veberic R., Slatnar A., Bizjak J., Stampar F., Mikulic-Petkovsek M. Anthocyanin composition of different wild and cultivated berry species. LWT - Food Science and Technology, 2015, 60(1): 509-517 CrossRef
  96. Tomás‐Barberán F.A., Clifford M.N. Flavanones, chalcones and dihydrochalcones — nature, occurrence and dietary burden. Journal of the Science of Food and Agriculture, 2000, 80(7), 1073-1080 CrossRef
  97. Miadoková E. Isoflavonoids — an overview of their biological activities and potential health benefits. Interdisciplinary Toxicology, 2009, 2(4): 211 CrossRef
  98. Posmyk M.M., Kontek R., Janas K.M. Antioxidant enzymes activity and phenolic compounds content in red cabbage seedlings exposed to copper stress. Ecotoxicology and Environmental Safety, 2009, 72(2): 596-602 CrossRef
  99. Sreevidya V.S., Srinivasa Rao C., Sullia S.B., Ladha J.K., Reddy P.M. Metabolic engineering of rice with soyabean isoflavone synthase for promoting nodulation gene expression in rhizobia. Journal of Experimental Botany, 2006, 57(9): 1957-1969 CrossRef
  100. Brooker N., Windorski J., Blumi E. Halogenated coumarins derivatives as novel seed protectants. Communications in Agricultural and Applied Biological Sciences, 2008, 73(2): 81-89.
  101. Murray R.D.H., Méndez J., Brown S.A. The natural coumarins: occurrence, chemistry and biochemistry. Wiley, New York, 1982.
  102. Serghini K., Pérez De Lugue A., Castejón‐Muñoz M., García‐Torres T., Jorrín J.V. Sunflower (Helianthus annuus L.) response to broomraoe (Orobanche cernua Loefl.) parasitism: induced synthesis and excretion of 7-hydroxylated simple coumarins. Journal of Experimental Botany, 2001, 52: 227-234 CrossRef
  103. Bruni R., Barreca D., Protti M., Brighenti V., Righetti L., Anceschi L., Mercolini L., Benvenuti S., Gattuso G., Pellati F. Botanical sources, chemistry, analysis, and biological activity of furanocoumarins of pharmaceutical interest. Molecules, 2019, 24(11): 2163 CrossRef
  104. Malekzadeh F. Evaluation of Several Bactericides as Seed Treatments for the Control of Black Rot of Crucifers and Studies on an Antibacterial Substance From Cauliflower Seed. (Parts I and II). Louisiana State University and Agricultural & Mechanical College ProQuest, 1962.
  105. Oluwole O., Fernando W.B., Lumanlan J., Ademuyiwa O., Jayasena V. Role of phenolic acid, tannins, stilbenes, lignans and flavonoids in human health — a review. International Journal of Food Science & Technology, 2022, 57(10): 6326-6335 CrossRef
  106. Aguilar-Hernández I., Afseth N.K., López-Luke T., Contreras-Torres F.F., Wold J.P., Ornelas-Soto N. Surface enhanced Raman spectroscopy of phenolic antioxidants: A systematic evaluation of ferulic acid, p-coumaric acid, caffeic acid and sinapic acid. Vibrational Spectroscopy, 2017, 89: 113-122 CrossRef
  107. Burns J., Yokota T., Ashihara H., Lean M.E.J., Crozier A. Plant foods and herbal sources of resveratrol. Journal of Agricultural and Food Chemistry, 2002, 50(11): 3337-3340 CrossRef
  108. The alkaloids: chemistry and physiology. Volume II. R.H.F. Manske, H.L. Holmes (eds.). Academic Press Inc., New York, 1952.
  109. Hobhouse H. Seeds of change: six plants that transformed mankind. Papermac, 1999.
  110. Scholl Y., Höke D., Dräger B. Calystegines in Calystegia sepium derive from the tropane alkaloid pathway. Phytochemistry, 2001, 58(6): 883-889 CrossRef
  111. Musk A.W., De Klerk N.H. History of tobacco and health. Respirology, 2003, 8(3): 286-290 CrossRef
  112. Cardozo Jr. E.L., Ferrarese-Filho O., Cardozo Filho L., de Lourdes Lucio Ferrarese M., Donaduzzi C.M., Sturion J.A. Methylxanthines and phenolic compounds in mate (Ilex paraguariensis St. Hil.) progenies grown in Brazil. Journal of Food Composition and Analysis, 2007, 20(7): 553-558 CrossRef
  113. Smit H.J. Theobromine and the pharmacology of cocoa. In: Methylxanthines. Handbook of Experimental Pharmacology, vol. 200 /B.B. Fredholm (ed.). Springer, Berlin, Heidelberg, 2011: 201-234 CrossRef
  114. Graser G., Hartmann T. Biosynthesis of spermidine, a direct precursor of pyrrolizidine alkaloids in root cultures of Senecio vulgaris L. Planta, 2000, 211: 239-245 CrossRef
  115. Ruiz M.A., Sotelo A. Chemical composition, nutritive value, and toxicology evaluation of Mexican wild lupins. Journal of Agricultural and Food Chemistry, 2001, 49(11): 5336-5339 CrossRef
  116. Suzuki H., Koike Y., Murakoshi I. Saito K. Subcellular localization of acyltransferases for quinolizidine alkaloid biosynthesis in Lupinus. Phytochemistry, 1996, 42(6): 1557-1562 CrossRef
  117. Bednarek P. Sulfur‐containing secondary metabolites from Arabidopsis thaliana and other Brassicaceae with function in plant immunity. ChemBioChem, 2012, 13(13): 1846-1859 CrossRef
  118. Venditti A., Bianc, A. Sulfur-containing secondary metabolites as neuroprotective agents. Current Medicinal Chemistry, 2020, 27(26): 4421-4436 CrossRef
  119. Kumar M., Kumar V., Roy D., Kushwaha R., Vaiswani S. Application of herbal feed additives in animal nutrition — a review. International Journal of Livestock Research, 2014, 4(9): 1-8.
  120. Miyasaki Y., Nichols W.S., Morgan M.A., Kwan J.A., Van Benschoten M.M., Kittell P.E., Hardy W.D. Screening of herbal extracts against multi‐drug resistant Acinetobacter baumannii. Phytotherapy Research, 2010, 24(8): 1202-1206 CrossRef
  121. Kipre B.G., Guessennd N.K., Koné M.W., Gbonon V., Coulibaly J.K., Dosso M. Antibacterial activity of the stem bark of Tieghemella Heckelii Pierre ex. A Chev against methicillin-resistant Staphylococcus aureus. BMC Complementary and Alternative Medicine, 2017, 17(1): 170 CrossRef
  122. Bevilacqua A., Corbo M.R., Sinigaglia M. In vitro evaluation of the antimicrobial activity of eugenol, limonene, and citrus extract against bacteria and yeasts, representative of the spoiling microflora of fruit juices. Journal of Food Protection, 2010, 73(5): 888-894 CrossRef
  123. Friedman M., Henika P.R., Mandrell R.E. Bactericidal activities of plant essential oils and some of their isolated constituents against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella entericaJournal of Food Protection, 2002, 65(10): 1545-1560 CrossRef
  124. Pontes E.K.U., Melo H.M., Nogueira J.W.A., Firmino N.C.S., de Carvalho M.G., Catunda Júnior F.E.A., Cavalcante T.T.A. Antibiofilm activity of the essential oil of citronella (Cymbopogon nardus) and its major com-ponent, geraniol, on the bacterial biofilms of Staphylococcus aureus. Food Science and Biotechnology, 2019, 28(3): 633-639 CrossRef
  125. Korotina O.L., Zubareva I.V., Yupatov Yu.G., Moiseev D.V., Generalov I.I. Immunopatologiya, allergologiya, infektologiya, 2013, 3: 10-21 (in Russ.).
  126. Pantev A., Ivancheva S., Staneva L., Serkedjieva J. Biologically active constituents of a polyphenol extract from Geranium sanguineum L. with anti-influenza activity. Zeitschrift für Naturforschung c, 2006, 61(7-8): 508-516 CrossRef
  127. Verma H., Patil P.R., Kolhapure R.M., Gopalkrishna V. Antiviral activity of the Indian medicinal plant extract, Swertia chirata against herpes simplex viruses: a study by in-vitro and molecular approach. Indian Journal of Medical Microbiology, 2008, 26(4), 322-326 CrossRef
  128. Stanojevic L.P., Marjanovic-Balaban Z.R., Kalaba V.D., Stanojevic J.S., Cvetkovic D.J. Chemical composition, antioxidant and antimicrobial activity of chamomile flowers essential oil (Matricaria chamomilla L.). Journal of Essential Oil Bearing Plants, 2016, 19(8): 2017-2028 CrossRef
  129. Novobilský A., Mueller-Harvey I., Thamsborg S.M. Condensed tannins act against cattle nematodes. Veterinary Parasitology, 201, 182(2-4): 213-220 CrossRef
  130. Daniel U.N., Ohalete C.N., Ibiam U.K., Okechukwu R. Medicinal plants effectiveness against helminths of cattle. Journal of Applied Biosciences, 2015, 86: 7900-7917 CrossRef
  131. Ghosh T., Kumar A., Sati A., Mondal B. C., Singh S. K., Kumar R. Effect of dietary supplementation of herbal feed additives (black cumin, garlic and turmeric) in combination with linseed oil on production performance of white leghorn laying chickens. Journal of Entomology and Zoology Studies, 2020, 8(6): 478-482.
  132. Panda S.S., Dhal N.K. Plants used in ethno-veterinary medicine by native people of Nawarangpur District, Odisha, India. World Journal of Pharmacy and Pharmaceutical Sciences, 2014, 3(7): 787-798.
  133. Ghosh S., Banerjee S., Sil P.C. The beneficial role of curcumin on inflammation, diabetes and neurodegenerative disease: a recent update. Food and Chemical Toxicology, 2015, 83: 111-124 CrossRef
  134. Nikolaev S.I., Melikhov V.V., Frolova M.V. Vestnik Rossiyskoy akademii sel’skokhozyaystvennykh nauk, 2009, 2: 68 (in Russ.).
  135. Wanapat M., Chanthakhoun V., Phesatcha K., Kang S. Influence of mangosteen peel powder as a source of plant secondary compounds on rumen microorganisms, volatile fatty acids, methane and microbial protein synthesis in swamp buffaloes. Livestock Science, 2014, 162: 126-133 CrossRef
  136. Abdalla A.L., Louvandini H., Sallam S.M.A.H., da Silva Bueno I.C., Tsai S.M., Figueira A.V.D.O. In vitro evaluation, in vivoquantification, and microbial diversity studies of nutritional strategies for reducing enteric methane production. Tropical Animal Health and Production, 2012, 44: 953-964 CrossRef
  137. Kim E.T., Guan L.L., Lee S.J., Lee S.M., Lee S.S., Lee I.D., Lee S.K., Lee S.S. Effects of flavonoid-rich plant extracts on in vitro ruminal methanogenesis, microbial populations and fermentation characteristics. Asian-Australasian Journal of Animal Sciences, 2015, 28(4): 530-537 CrossRef
  138. Macheboeuf D., Morgavi D.P., Papon Y., Mousset J.-L., Arturo-Schaan M. Dose-response effects of essential oils on in vitro fermentation activity of the rumen microbial population. Animal Feed Science and Technology, 2008, 145(1-4): 335-350 CrossRef
  139. Busquet M., Calsamiglia S., Ferret A., Cardozo P.W., Kamel C. Effects of cinnamaldehyde and garlic oil on rumen microbial fermentation in a dual flow continuous culture. Journal of Dairy Science, 2005, 88(7): 2508-2516 CrossRef
  140. Konda S., Onodera R., Kanchanasatit E., Boonsaen P., Sawanon S., Nagashima K., Suzuki Y., Koike S., Kobayashi Y. Effect of cashew nut shell liquid feeding on fermentation and microbiota in the rumen of Thai native cattle and swamp buffaloes. Livestock Science, 2019, 226: 99-106 CrossRef
  141. Groot M.J., Kleijer-Ligtenberg G., Van Asseldonk T., Hansman H. Natural dairy cow health: a guide to keeping your herd healthy with herbs and other natural products. RIKILT Wageningen UR, 2011.
  142. Soroor M.E.N., Moeini M.M. The influence of ginger (Zingiber officinale) on in vitro rumen fermentation patterns. Annual Research & Review in Biology, 2014, 5(1): 54-63 CrossRef
  143. Chaturvedi I., Dutta T.K., Singh P.K., Sharma A. Effect of combined herbal feed additives on methane, total gas production and rumen fermentation. Bioinformation, 2015, 11(5): 261-266 CrossRef
  144. Jain P., Mohini M., Singhal K.K., Tyagi A.K. Effect of herbal mixture supplementation on methane emission and milk production in cattle. Indian Journal of Animal Nutrition, 2011, 28(4): 377-384.
  145. García-González R., Dehority B.A., Lopez S. Ruminal bacteria counts from in vitro cultures upon the addition of medicinal plants that modify the fermentation. XI Jornadas sobre Producción Animal.Zaragoza, Spain, 2005, I & II: 614-616.
  146. Kholif A.E., Matloup O.H., Morsy T.A., Abdo M.M., Abu Elella A.A., Anele U.Y., Swanson K.C. Rosemary and lemongrass herbs as phytogenic feed additives to improve efficient feed utilization, manipulate rumen fermentation and elevate milk production of Damascus goats. Livestock Science, 2017, 204: 39-46 CrossRef
  147. Wanapat M., Cherdthong A., Pakdee P., Wanapat S. Manipulation of rumen ecology by dietary lemongrass (Cymbopogon citratus Stapf.) powder supplementation. Journal of Animal Science, 2008, 86(12): 3497-3503 CrossRef
  148. Kulakova T.S., Tretyakov E.A., Fomina L.L., Zakrepina E.N., Zhuravlyova S.G. Effects of adsorbent and phytobiotic on density of rumen infusoria and cow milk production. Russian Agricultural Sciences, 2019, 45: 194-196 CrossRef
  149. Burt S. Essential oils: their antibacterial properties and potential applications in foods — a review. International Journal of Food Microbiology, 2004, 94(3): 223-253 CrossRef
  150. Benchaar C., Chaves A.V., Fraser G.R., Beauchemin K.A., McAllister T.A. Effects of essential oils and their components on in vitro rumen microbial fermentation. Canadian Journal of Animal Science, 2007, 87(3): 413-419 CrossRef
  151. Skandamis P., Koutsoumanis K., Fasseas K., Nychas G.J. Inhibition of oregano essential oil and EDTA on Escherichia coli O157: H7. Italian Journal of Food Science, 2001, 13(1): 65-75 CrossRef
  152. Carson C.F., Mee B.J., Riley T.V. Mechanism of action of Melaleuca alternifolia (tea tree) oil on Staphylococcus aureus determined by time-kill, lysis, leakage, and salt tolerance assays and electron microscopy. Antimicrobial Agents and Chemotherapy, 2002, 46(6): 1914-1920 CrossRef
  153. Sikkema J.A.N., de Bont J.A., Poolman B. Mechanisms of membrane toxicity of hydrocarbons. Microbiological Reviews, 1995, 59(2): 201-222 CrossRef
  154. Ultee A., Kets E.P., Alberda M., Hoekstra F.A., Smid E.J. Adaptation of the food-borne pathogen Bacillus cereus to carvacrol. Archives of Microbiology, 2000, 174: 233-238 CrossRef
  155. Ultee A., Bennik M.H.J., Moezelaar R.The phenolic hydroxyl group of carvacrol is essential for action against the food-borne pathogen Bacillus cereus. Applied and Environmental Microbiology, 2002, 68(4): 1561-1568 CrossRef
  156. Cox S.D., Mann C.M., Markham J.L., Bell H.C., Gustafson J.E., Warmington J.R., Wyllie S.G. The mode of antimicrobial action of the essential oil of Melaleuca alternifolia (tea tree oil). Journal of Applied Microbiology, 2000, 88(1): 170-175 CrossRef
  157. Ultee A., Kets E.P.W., Smid E.J. Mechanisms of action of carvacrol on the food-borne pathogen Bacillus cereus. Applied and Environmental Microbiology, 1999, 65(10): 4606-4610 CrossRef
  158. Davidson P.M., Taylor T.M., Schmidt S.E. Chemical preservatives and natural antimicrobial compounds. In:  Food microbiology: fundamentals and frontiers. M.P. Doyle, R.L. Buchanan (eds.). 2012: 765-801 CrossRef
  159. Kondrashova K.S., Kosyan D.B., Atlanderova K.N., Lebedev S.V. Prospects of antiquorum substances as an alternative to antibiotic therapy in animal husbandry (review). Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2020, 55(6): 1073-1089 CrossRef
  160. Ku-Vera J.C., Jiménez-Ocampo R., Valencia-Salazar S.S., Montoya-Flores M.D., Molina-Botero I.C., Arango J., Gómez-Bravo C.A., Aguilar-Pérez C.F., Solorio-Sánchez F.J. Role of secondary plant metabolites on enteric methane mitigation in ruminants. Frontiers in Veterinary Science, 2020, 7: 584 CrossRef
  161. Jouany J.-P., Morgavi D.P. Use of ‘natural’ products as alternatives to antibiotic feed additives in ruminant production. Animal, 2007, 1(10): 1443-1466 CrossRef
  162. Han Y., Chen W., Sun Z. Antimicrobial activity and mechanism of limonene against Staphylococcus aureusJournal of Food Safety, 2021, 41(5): e12918 CrossRef
  163. Mirza Z.R.M.H., Hasan T., Seidel V., Yu J. Geraniol as a novel antivirulence agent against bacillary dysentery-causing Shigella sonnei. Virulence, 2018, 9(1): 450-455 CrossRef
  164. Yao X., Zhu X., Pan S., Fang Y., Jiang F., Phillips G.O., Xu X. Antimicrobial activity of nobiletin and tangeretin against Pseudomonas. Food Chemistry, 2012, 132(4): 1883-1890 CrossRef
  165. Feng D., Zhang A., Yang Y., Yang P. Coumarin‐containing hybrids and their antibacterial activities. Archiv der Pharmazie, 2020, 353(6): 1900380 CrossRef
  166. Landau E., Shapira R. Effects of subinhibitory concentrations of menthol on adaptation, morphological, and gene expression changes in enterohemorrhagic Escherichia coli. Applied and Environmental Microbiology, 2012, 78(15): 5361-5367 CrossRef
  167. Memariani H., Memariani M., Ghasemian A. An overview on anti-biofilm properties of quercetin against bacterial pathogens. World Journal of Microbiology and Biotechnology, 2019, 35: 143 CrossRef
  168. Calsamiglia S., Busquet M., Cardozo P.W., Castillejos L., Ferret A. Invited review: essential oils as modifiers of rumen microbial fermentation. Journal of Dairy Science, 2007, 90(6): 2580-2595 CrossRef
  169. Pauli A., Schilcher H. In vitro antimicrobial activities of essential oils monographed in the European Pharmacopoeia 6th Edition. In: Handbook of essential oils: science, technology, and applications. K. Hüsnü Can Bașer, G. Buchbauer (eds.)., CRC Press, Boca Raton, 2010: 353-548.
  170. Patra A.K., Yu Z. Essential oils affect populations of some rumen bacteria in vitro as revealed by microarray (RumenBactArray) analysis. Frontiers in Microbiology, 2015, 6: 297 CrossRef
  171. Frankič T., Voljč M., Salobir J., Rezar V. Use of herbs and spices and their extracts in animal nutrition. Acta agriculturae Slovenica, 2009, 94(2): 95-102 CrossRef
  172. Sukhanova S.F., Azaubaeva G.S. Vestnik Kurganskoy GSKhA, 2015, 1(13): 55-59 (in Russ.).
  173. Juliani H.R., Koroch A.R., Simon J.E. Chemical diversity of essential oils of Ocimum species and their associated antioxidant and antimicrobial activity. In: Essential oils and aromas: Green extractions and applications. K. Chemat, F. Varshney, V.K. Allaf (eds.). Har Krishan Bhalla & Sons, Dehradun, 2009: 284-295.
  174. Tajodini M., Moghbeli P., Saeedi H.R., Effati M. The effect of medicinal plants as a feed additive in ruminant nutrition. Iranian Journal of Applied Animal Science, 2014, 4(4): 681-686.
  175. Yang W.Z., Benchaar C., Ametaj B.N., Chaves A.V., He M.L., McAllister T.A. Effects of garlic and juniper berry essential oils on ruminal fermentation, site and extent of digestion in lactating cows. Journal of Dairy Science, 2007, 90(12): 5671-5681 CrossRef
  176. Jeshari M., Riasi A., Mahdavi A.H., Khorvash M., Ahmadi F. Effect of essential oils and distillation residues blends on growth performance and blood metabolites of Holstein calves weaned gradually or abruptly. Livestock Science, 2016, 185: 117-122 CrossRef
  177. Tapki I., Ozalpaydin H.B., Tapki N., Aslan M., Selvi M.H. Effects of oregano essential oil on reduction of weaning age and increasing economic efficiency in Holstein Friesian calves. Pakistan Journal of Zoology, 2020, 52(2): 745 CrossRef
  178. Hashemzadeh-Cigari F., Khorvash M., Ghorbani G.R., Kadivar M., Riasi A., Zebeli Q. Effects of supplementation with a phytobiotics-rich herbal mixture on performance, udder health, and metabolic status of Holstein cows with various levels of milk somatic cell counts. Journal of Dairy Science, 2014, 97(12): 7487-7497 CrossRef
  179. Stefańska B., Sroka J., Katzer F., Goliński P., Nowak W. The effect of probiotics, phytobiotics and their combination as feed additives in the diet of dairy calves on performance, rumen fermentation and blood metabolites during the preweaning period. Animal Feed Science and Technology, 2021, 272: 114738 CrossRef
  180. Korotkiy V.P., Yurina N.A., Yurin D.A., Buryakov N.P., Ryzhov V.A., Marisov S.S. Effektivnoe zhivotnovodstvo, 2020, 4(161): 121-123 (in Russ.).
  181. Terent’ev V.I., Anikienko T.I. Vestnik KrasGAU, 2011, 5(56): 163-166 (in Russ.).
  182. Nekrasov R.V., Chabaev M.G., Ushakova N.A. Pravdin V.G., Kravtsova L.Z. IzvestiyaOrenburgskogogosudarstvennogoagrarnogouniversiteta, 2012, 6(38): 225-228 (in Russ.).
  183. Belanche A., Newbold C.J., Morgavi D.P., Bach A., Zweifel B., Yáñez-Ruiz D.R. A meta-analysis describing the effects of the essential oils blend agolin ruminant on performance, rumen fermentation and methane emissions in dairy cows. Animals, 2020, 10(4): 620 CrossRef
  184. Flavonoids in health and disease. C.A. Rice-Evans, L. Packer (eds.). Marcel Dekker Inc., New York, 2003.
  185. Heim K.E., Tagliaferro A.R., Bobilya D.J. Flavonoid antioxidants: chemistry metabolism and structure activity relationships. Journal of Nutritional Biochemistry, 2002, 13(10): 572-584 CrossRef
  186. Hollman P.C.H., Katan M.B. Dietary flavonoids: intake health effects and bioavailability. Food and Chemical Toxicology, 1999, 37(9-10): 937-942 CrossRef
  187. Nakatani N. Antioxidants from spices and herbs. In: Natural antioxidants. Chemistry, health effects and applications. F.  Shahidi (ed.). AOCS Press, Champaign, 1996: 64-75.
  188. Wei A., Shibamoto T. Antioxidant activities and volatile constituents of various essential oils. Journal Agriculture and Food Chemistry, 2007, 55(5): 1737-1742 CrossRef
  189. Muanda F., Koné D., Dicko A., Soulimani R., Younos C. Phytochemical composition and antioxidant capacity of three Malian medicinal plant parts. Evidence-Based Complementary and Alternative Medicine, 2011: 674320 CrossRef
  190. Taga I., Lan C.Q., Altosaar I. Plant essential oils and mastitis disease: their potential inhibitory effects on pro-inflammatory cytokine production in response to bacteria related inflammation Natural Product Communications, 2012, 7(5): 1934578X1200700534 CrossRef
  191. Spelman K., Burns J.J., Nichols D., Winters N., Ottersberg S., Tenborg M. Modulation of cytokine expression by traditional medicines: a review of herbal immunomodulators. Alternative Medicine Review, 2006, 11(2): 128-150.
  192. Mahima, Rahal A., Deb R., Latheef S.K., Samad A.H., Tiwari R., Verma A.K., Kumar A., Dhama K. Immunomodulatory and therapeutic potentials of herbal, traditional/indigenous and ethnoveterinary medicines. Pakistan Journal of Biological Sciences, 2012, 15(16): 754-774 CrossRef
  193. Churchill M., Chadburn A., Bilinski R.T., Bertagnolli M.M. Inhibition of intestinal tumors by curcumin is associated with changes in the intestinal immune cell profile. Journal of Surgical Research, 2000, 89(2): 169-175 CrossRef
  194. Lavinia S., Gabi D., Drinceanu D., Stef D., Daniela M., Julean C., Ramona T., Corcionivoschi N. The effect of medicinal plants and plant extracted oils on broiler duodenum morphology and immunological profile. Romanian Biotechnological Letters, 2009, 14(4): 4606-4614.
  195. Luseba D., Tshisikhawe M.P. Medicinal plants used in the treatment of livestock diseases in Vhembe region, Limpopo province, South Africa. Journal of Medicinal Plants Research, 2013, 7(10): 593-601.
  196. Kumar R., Bharati K.A. New claims in folk veterinary medicines from Uttar Pradesh, India. Journal of Ethnopharmacology, 2013, 146(2): 581-593 CrossRef
  197. Perumal P., Veeraselvam M., Nahak A.K. Herbal treatment in animal reproduction. International Journal of Bio-resource and Stress Management, 2013, 4(3): 460-467.
  198. Dutt R., Mehrotra S., Shanker U., Singh G. Effect of Murraya koenigii and Aegle marmelos feeding on anestrus buffaloes. Indian Journal of Animal Reproduction, 2011, 32(1): 47-49.
  199. Ahmed H., Jahan S., Salman M.M., Ullah F. Stimulating effects of Quercetin (QUE) in tris citric acid extender on post thaw quality and in vivo fertility of buffalo (Bubalus bubalis) bull spermatozoa. Theriogenology, 2019, 134: 18-23 CrossRef
  200. Kumar S., Mehla R.K., Dang A.K. Use of shatavari (Asparagus racemosus) as a galactopoietic and therapeutic herb — a review. Agricultural Reviews, 2008, 29(2): 132-138.
  201. Cross D.E., McDevitt R.M., Hillman K., Acamovic T. The effect of herbs and their associated essential oils on performance, dietary digestibility and gut microflora in chickens from 7 to 28 days of age. British Poultry Science, 2007, 48(4): 496-506 CrossRef
  202. Yang Y., Iji P.A., Choct M. Dietary modulation of gut microflora in broiler chickens: a review of the role of six kinds of alternatives to in-feed antibiotics. World's Poultry Science Journal, 2009, 65(1): 97-114 CrossRef
  203. McGimpsey J.A., Douglas M.H., Van Klink J.W., Beauregard D.A., Perry N.B. Seasonal variation in essential oil yield and composition from naturalized Thymus vulgaris L.in New Zealand. Flavour and Fragrance Journal, 1994, 9(6): 347-352 CrossRef
  204. Marino M., Bersani C., Comi G. Antimicrobial activity of the essential oils of Thymus vulgaris L. measured using a bioimpedometric method. Journal of Food Protection, 1999, 62(9): 1017-1023 CrossRef
  205. Giannenas I., Florou-Paneri P., Papazahariadou M., Christaki E., Botsoglou N.A., Spais A.B. Effect of dietary supplementation with oregano essential oil on performance of broilers after experimental infection with Eimeria tenella. Archives of Animal Nutrition, 2003, 57(2): 99-106 CrossRef
  206. Sarica S., Ciftci A., Demir E., Kilinc K., Yildirim Y. Use of an antibiotic growth promoter and two herbal natural feed additives with and without exogenous enzymes in wheat based broiler diets. South African Journal of Animal Science, 2005, 35(1): 61-72 CrossRef
  207. Terent’ev V.I., Anikienko T.I. Vestnik Krasnoyarskogo gosudarstvennogo agrarnogo universiteta, 2011, 8: 246-249 (in Russ.).
  208. Kolesnik N.S., Bogolyubova N.V., Zelenchenkova A.A. The effect of different classes of tannins on methanogenesis in ruminants (review).Sel'skokhozyaistvennaya biologiya [Agricultural Biology], 2024, 59(2): 221-236 CrossRef
  209. Ahmed M.G., Elwakeel E.A., El-Zarkouny S.Z., Al-Sagheer A.A. Environmental impact of phytobiotic additives on greenhouse gas emission reduction, rumen fermentation manipulation, and performance in ruminants: an updated review. Environ. Sci. Pollut. Res. Int., 2024, 31(26): 37943-37962 CrossRef
  210. Wang J., Deng L., Chen M., Che Y., Li L., Zhu L., Chen G., Feng T. Phytogenic feed additives as natural antibiotic alternatives in animal health and production: a review of the literature of the last decade. Anim. Nutr., 2024, 17: 244-264 CrossRef

 

back

 


CONTENTS

 

Full article PDF (Rus)