پژوهشهای علوم دامی ایران

پژوهشهای علوم دامی ایران

اثر اسانس آبی گیاه زوفا (Hyssopus officinalis L.) بر فراسنجه‌های تخمیری، تجزیه‌پذیری مواد مغذی و تولید متان شکمبه‌ای در شرایط برون‌تنی

نوع مقاله : مقاله پژوهشی

نویسنده
گروه علوم دامی، مجتمع آموزش عالی تربت‌جام، تربت‌جام، ایران
چکیده
استفاده از افزودنی‌های طبیعی برای تعدیل تخمیر شکمبه و کاهش تولید متان به‌عنوان رویکردی پایدار در تغذیه نشخوارکنندگان اهمیت یافته است. اسانس گیاهی زوفا (Hyssopus officinalis L.) با ترکیبات زیست‌فعال خود می‌تواند اکوسیستم میکروبی شکمبه را تحت تأثیر قرار دهد. این پژوهش با هدف بررسی تأثیر سطوح مختلف اسانس گیاه کامل زوفا (۰، ۵۰، ۱۰۰، ۱۵۰ و ۲۰۰ میلی‌گرم در لیتر) بر تولید گاز و متان، فراسنجه‌های تخمیری و شاخص‌های میکروبی شکمبه­ گوسفند در شرایط برون­تنی انجام شد. نتایج نشان داد که افزودن اسانس زوفا موجب کاهش معنی‌دار تولید متان (تا ۳۱ درصد در سطح ۲۰۰ میلی‌گرم در لیتر) و تولید گاز تجمعی (میلی­لیتر) در تمام زمان‌های انکوباسیون گردید (05/0>P). جمعیت پروتوزوآی کل با افزایش سطح اسانس، کاهش خطی نشان داد و در سطح ۲۰۰ میلی‌گرم در لیتر به‌میزان ۳۳ درصد کمتر از شاهد بود (05/0>P). غلظت اسیدهای چرب فرار کل تا سطح ۱۰۰ میلی‌گرم در لیتر افزایش و سپس کاهش یافت (05/0>P). توده میکروبی تولیدی و راندمان سنتز میکروبی در سطح ۱۰۰ میلی‌گرم در لیتر به‌‌ترتیب ۱۹ و ۲۰ درصد بهبود یافت (05/0>P). به­طورکلی، سطح ۱۰۰ میلی‌گرم در لیتر به­عنوان سطح بهینه برای تعدیل فراسنجه­های تخمیر شکمبه­ای شناسایی شد، زیرا ضمن کاهش معنی‌دار تولید متان، کارآیی میکروبی را بهبود بخشیده و در عین حال قابلیت هضم مواد مغذی را حفظ نمود. این سطح می‌تواند به‌عنوان راهکاری مؤثر برای بهبود تخمیر شکمبه و کاهش انتشار متان پیشنهاد شود.
کلیدواژه‌ها
موضوعات

عنوان مقاله English

Effects of Hyssop (Hyssopus officinalis L.) Essential Oil on Ruminal Fermentation Parameters, Nutrient Degradability, and Methane Production in vitro

نویسنده English

Mohsen Kazemi
Department of Animal Science, Faculty of Agriculture and Animal Science, University of Torbat-e Jam, Torbat-e Jam, Iran
چکیده English

Introduction: The utilization of natural feed additives to modulate rumen fermentation processes and mitigate enteric methane emissions has garnered considerable attention as a sustainable nutritional strategy in ruminant production systems. Plant-derived essential oils (EOs), with their complex bioactive profiles, offer a promising alternative for shifting the rumen microbial ecosystem toward improved fermentation efficiency. Hyssop (Hyssopus officinalis L.), a perennial herb belonging to the Lamiaceae family, is widely recognized for its medicinal and aromatic properties. The essential oil extracted from this plant contains numerous biologically active components, notably pinocamphone, β-pinene, and various sesquiterpenes, which collectively exhibit potent antimicrobial, antifungal, and antioxidant activities. These multifaceted biological properties suggest substantial potential for optimizing rumen fermentation dynamics and improving nutrient utilization. The present study was therefore designed to systematically evaluate the effects of different inclusion levels of whole Hyssop essential oil (HEO) on in vitro gas production kinetics, methane emission patterns, key fermentation parameters, and microbial indices in ruminal fluid. The central hypothesis was that, due to its antimicrobial properties, HEO could establish an optimal balance between suppressing methane production and maintaining or even improving ruminal fermentation efficiency at a specific concentration. Therefore, this investigation aimed to assess the impact of HEO on ruminal methane output, volatile fatty acid profile, nutrient degradability, and microbial protein synthesis efficiency to identify its optimal dietary inclusion level.
Materials and Methods: The experiment was conducted in a completely randomized design with five treatments and four replicates. Treatments included different levels of HEO (0, 50, 100, 150, and 200 mg/L of culture medium). The essential oil was obtained via hydrodistillation using a Clevenger apparatus from the aerial parts of the plant collected at full flowering. Rumen fluid was collected from three fistulated male sheep (30 ± 3.5 kg body weight) fed a diet consisting of wheat straw and concentrate. The in vitro gas production technique was used, and samples were incubated at 39°C for 96 hours. Gas production was measured at 3, 6, 9, 12, 24, 48, 72, and 96 hours. Methane production was assessed at 24 hours by absorbing carbon dioxide with a 10 M NaOH solution. After 24 hours of incubation, additional fermentation and microbial parameters were evaluated. These post-incubation analyses included measurements of pH, ammonia-nitrogen concentration, total volatile fatty acids (TVFA) concentration, and total protozoal count using a Neubauer chamber. Additionally, degradability of dry matter (DM), organic matter (OM), and neutral detergent fiber (NDF) were determined. Microbial biomass yield and microbial synthesis efficiency were calculated based on truly degraded organic matter and gas production data.
Results and Discussion: The addition of HEO significantly and dose-dependently reduced in vitro methane production. The effect was most pronounced at the highest dose, where methane production decreased by 31% at 200 mg/L compared with the control treatment (P < 0.05). This reduction is likely attributed to the direct inhibitory effect of the HEO bioactive compounds, particularly pinocamphone, on methanogenic archaea and protozoa. Cumulative gas production decreased significantly at all incubation time points compared to the control (P<0.05). Total protozoal population declined linearly with increasing essential oil levels, showing a substantial 33% reduction at 200 mg/L compared to the control (P<0.05), highlighting the strong antiprotozoal activity of the essential oil. TVFA concentration showed a quadratic response (P<0.05), increasing up to the 100 mg/L level and then decreasing at higher doses, indicating a dual stimulatory and inhibitory effect on microbial fermentation. Notably, the 100 mg/L treatment significantly increased microbial biomass yield and microbial synthesis efficiency by 19% and 20%, respectively (P<0.05), indicating a more efficient allocation of digested nutrients to microbial biomass production. Conversely, degradability of DM, OM, and NDF decreased linearly with increasing essential oil levels (P<0.05), reflecting a general inhibitory effect on fibrolytic microbial activity at higher concentrations.
Conclusion: At an inclusion level of 100 mg/L, HEO achieved a significant methane reduction (14.3%) while improving microbial protein synthesis efficiency and maintaining acceptable nutrient digestibility. This specific level of HEO may therefore serve as an effective natural strategy for enhancing the efficiency of rumen fermentation and reducing the environmental impact of ruminant production through lower methane emissions. For practical application, further in vivo trials are recommended to validate these promising in vitro findings and to determine the appropriate dietary inclusion rate.

کلیدواژه‌ها English

Digestibility
Gas production
Herbal essential oil
Microbial synthesis efficiency
Protozoa population

Authors retain the copyright. This is an open access article distributed under Creative Commons Attribution 4.0 International License (CC BY 4.0)

  1. Alabi, J. O., Okedoyin, D. O., Anotaenwere, C. C., Wuaku, M., Gray, D., Adelusi, O. O., Ike, K. A., Olagunju, L. K., Dele, P. A., & Anele, U. Y. (2023). Essential oil blends with or without fumaric acid influenced in vitro rumen fermentation, greenhouse gas emission, and volatile fatty acids production of a total mixed ration. Ruminants, 3(4), 373-384. https://doi.org/10.3390/ruminants3040031
  2. Barnett, A. J. G., & Reid, R. (1957). Studies on the production of volatile fatty acids from grass in artificial rumen. 1. Volatile fatty acids production from fresh grasses. The Journal of Agricultural Science, 48(3), 315-321. https://doi.org/10.1017/S0021859600031671
  3. Benetel, G., Silva, T. D. S., Fagundes, G. M., Welter, K. C., Melo, F. A., Lobo, A. A., Muir, J. P., & Bueno, I. C. S. (2022). Essential oils as in vitro ruminal fermentation manipulators to mitigate methane emission by beef cattle grazing tropical grasses. Molecules, 27(7), 2227. https://doi.org/10.3390/molecules27072227
  4. Blümmel, M., Makkar, H. P. S., & Becker, K. (1997). In vitro gas production: A technique revisited. Journal of Animal Physiology and Animal Nutrition, 77(1-5), 24-34. https://doi.org/10.1111/j.1439-0396.1997.tb00734.x
  5. Bodas, R., Prieto, N., García-González, R., Andrés, S., Giráldez, F. J., & López, S. (2012). Manipulation of rumen fermentation and methane production with plant secondary metabolites. Animal Feed Science and Technology, 176(1-4), 78-93. https://doi.org/10.1016/j.anifeedsci.2012.07.010
  6. Brice, R. M., Dele, P. A., Ike, K. A., Shaw, Y. A., Olagunju, L. K., Orimaye, O. E., Subedi, K., & Anele, U. Y. (2022). Effects of essential oil blends on in vitro apparent and truly degradable dry matter, efficiency of microbial production, total short-chain fatty acids and greenhouse gas emissions of two dairy cow diets. Animals, 12(17), 2185. https://doi.org/10.3390/ani12172185
  7. Calsamiglia, S., Busquet, M., Cardozo, P. W., Castillejos, L., & Ferret, A. (2007). Essential oils as modifiers of rumen microbial fermentation. Journal of Dairy Science, 90(6), 2580-2595. https://doi.org/10.3168/jds.2006-644
  8. Chouchen, R., Attia, K., Darej, C., & Moujahed, N. (2018). Potential of eucalyptus (Eucalyptus camaldulensis) essential oil to modify in vitro rumen fermentation in sheep. Journal of Applied Animal Research, 46(1), 1220-1225. https://doi.org/10.1080/09712119.2018.1486318
  9. Dehority, B. A. (2003). Rumen Microbiology. British Library Cataloguing in Publication Data, 372 p.
  10. Dorantes-Iturbide, G., Orzuna-Orzuna, J. F., Lara-Bueno, A., Mendoza-Martínez, G. D., Miranda-Romero, L. A., & Lee-Rangel, H. A. (2022). Essential oils as a dietary additive for small ruminants: A meta-analysis on performance, rumen parameters, serum metabolites, and product quality. Veterinary Sciences, 9(9), 475. https://doi.org/10.3390/vetsci9090475
  11. Fathiazad, F., Mazandarani, M., & Hamedeyazdan, S. (2011). Phytochemical analysis and antioxidant activity of Hyssopus officinalis from Iran. Advanced Pharmaceutical Bulletin, 1(2), 63-67. https://doi.org/10.5681/apb.2011.009
  12. Fievez, V., Babaymo, O. J., & Demeyer, D. (2005). Estimation of direct and indirect gas production in syringes: A tool to estimate short chain fatty acid production that requires minimal laboratory facilities. Animal Feed Science and Technology, 123-124(part 1), 197-210. https://doi.org/10.1016/j.anifeedsci.2005.05.001
  13. Goncearius, M., & Balmus, Z. (2013). Diversity of the essential oil content and chemical composition of Hyssopus officinalis genotypes. Muzeul Olteniei Craiova. Studii şi comunicări. Ştiinţele Naturii, 29(1), 171-178.
  14. Hatipoğlu, G., Sökmen, M., Bektaş, E., Daferera, D., Sökmen, A., Demir, E., & Şahin, H. (2013). Automated and standard extraction of antioxidant phenolic compounds of Hyssopus officinalis ssp. angustifolius. Industrial Crops and Products, 43: 427-433. https://doi.org/10.1016/j.indcrop.2012.07.028
  15. Kazemi, M. (2019). Effects of hexane extract of medicinal plant Artemisia aucheri on fermentation characteristics, gas production parameters, and degradability under in vitro conditions. Iranian Journal of Medicinal and Aromatic Plants, 35(6), 902-913. (In Persian). https://doi.org/10.22092/ijmapr.2019.125475.2524  
  16. Kazemi, M., & Eskandari Torbaghan, Y. (2019). The effect of oil extracted from Borago officinalis whole plant at flowering stage on some ruminal fermentation parameters of sheep. Veterinary Clinical Pathology, 13(3), 305-320. (In Persian). https://doi.org/10.30495/jvcp.2019.669193  
  17. Kazemi, M., & Mokhtarpour, A. (2020). The effect of Nepeta glomerulosa essential oil on in vitro gas production and ruminal fermentation. Journal of Livestock Science and Technologies, 8(2), 1-8. https://doi.org/10.22103/jlst.2020.16510.1328
  18. Kazemi, M., & Mokhtarpour, A. (2021). In vitro and in vivo evaluation of some tree leaves as forage sources in the diet of Baluchi male lambs. Small Ruminant Research, 201, 106416. https://doi.org/10.1016/j.smallrumres.2021.106416
  19. Khiaosa-Ard, R., & Zebeli, Q. (2013). Meta-analysis of the effects of essential oils and their bioactive compounds on rumen fermentation characteristics and feed efficiency in ruminants. Journal of Animal Science, 91(4), 1819-1830. https://doi.org/10.2527/jas.2012-5691
  20. Kizil, S., Hasimi, N., Tolan, V., Kilinc, E., & Karatas, H. (2010). Chemical composition, antimicrobial and antioxidant activities of hyssop (Hyssopus officinalis) essential oil. Notulae Botanicae Horti Agrobotanici Cluj-Napoca, 38(3), 99-103. https://doi.org/10.15835/nbha3834788
  21. Komolong, M. K., Barber, D. G., & McNeill, D. M. (2001). Post-ruminal protein supply and N retention of weaner sheep fed on a basal diet of lucerne hay (Medicago sativa) with increasing levels of quebracho tannins. Animal Feed Science and Technology, 92(1-2), 59-72. https://doi.org/10.1016/S0377-8401(01)00246-2
  22. Ma, X., Ma, X., Ma, Z., Wang, J., Sun, Z., Yu, W., Li, F., & Ding, J. (2014). Effect of Hyssopus officinalis on inhibiting airway inflammation and immune regulation in a chronic asthmatic mouse model. Experimental and Therapeutic Medicine, 8(5), 1371-1374. https://doi.org/10.3892/etm.2014.1978
  23. Makkar, H. P. S. (2010). In vitro screening of feed resources for efficiency of microbial protein synthesis. In: In vitro screening of plant resources for extra-nutritional attributes in ruminants. Springer, New York, pp. 106-144. https://doi.org/10.1007/978-90-481-3297-3_7
  24. Mazzanti, G., Battinelli, L., & Salvatore, G. (1998). Antimicrobial properties of the linalol-rich essential oil of Hyssopus officinalis var decumbens (Lamiaceae). Flavour and Fragrance Journal, 13(5), 289-294. https://doi.org/10.1002/(SICI)1099-1026(1998090)13:5<289::AID-FFJ750>3.0.CO;2-A
  25. Mehdipour Golbotte, M., Malecky, M., Aliarabi, H., & Zamani, P. (2022). Effects of different levels of the savory essential oil on in vitro ruminal fermentation parameters, microbial protein synthesis and protozoal populations in two diets supplemented with fish and soybean oil. Journal of Ruminant Research, 10(3), 87-110. (In Persian). https://doi.org/10.22069/ejrr.2022.20101.1845
  26. Menke, K.H., & Steingass, H. (1988). Estimation of the energetic feed value obtained from chemical analysis and in vitro gas production using rumen fluid. Animal Research Development, 28: 7-55.
  27. NRC. (2007). Nutrient requirements of small ruminants: Sheep, goats, cervids, and new world camelids. 6th Washington, DC: National Academy Press. 384p.
  28. Ørskov, E.R., & McDonald, I. (1979). The estimation of protein degradability in the rumen from incubation measurements weighted according to rate of passage. Journal of Agricultural Science, 92(2), 499-503. https://doi.org/10.1017/S0021859600063048
  29. Pandey, V., Verma, R.S., Chauhan, A., & Tiwari, R. (2014). Compositional variation in the leaf, flower and stem essential oils of Hyssop (Hyssopus officinalis) from Western Himalaya. Journal of Herbal Medicine, 4(2), 89-95. https://doi.org/10.1016/j.hermed.2013.12.001
  30. Patra, A.K. (2007). Nutritional management in organic livestock farming for improved ruminant health and production: An overview. Livestock Research for Rural Development, 19(3), 41.
  31. Patra, A.K. (2011). Effects of essential oils on rumen fermentation, microbial ecology and ruminant production. Asian Journal of Animal and Veterinary Advances, 6: 416-428. https://doi.org/10.3923/ajava.2011.416.428  
  32. Patra, A.K. (2015). Urea/ammonia metabolism in the rumen and toxicity in ruminants. In Rumen Microbiology: From Evolution to Revolution (pp. 329-341). Springer, New Delhi. https://doi.org/10.1007/978-81-322-2401-3_22
  33. Patra, A.K. & Yu, Z. (2012). Effects of essential oils on methane production and fermentation by, and abundance and diversity of, rumen microbial populations. Applied and Environmental Microbiology, 78(12), 4271-4280. https://doi.org/10.1128/AEM.00309-12
  34. Pepeta, B.N., Hassen, A., & Tesfamariam, E.H. (2024). Quantifying the impact of different dietary rumen modulating strategies on enteric methane emission and productivity in ruminant livestock: A meta-analysis. Animals, 14(5), 763. https://doi.org/10.3390/ani14050763
  35. Sallam, S.M.A., & Abdalla, A.L. (2011). Antimethanogenic and antiprotozoal effect of some essential oils in vitro. Egyptian Journal of Animal Production, 48(2), 203-215. https://doi.org/10.21608/ejap.2011.94074
  36. Saral, Ö., Baltaş, N. & Karaköse, M. (2024). An inhibition potential on some metabolic enzymes (urease and xanthine oxidase), essential oil contents and antioxidant effect of Sideritis lanata Chemical Papers, 78(15), 8211-8217. https://doi.org/10.1007/s11696-024-03661-6
  37. Selje, N., Hoffmann, E.M., Muetzel, S., Ningrat, R., Wallace, R.J., & Becker, K. (2007). Results of a screening programme to identify plants or plant extracts that inhibit ruminal protein degradation. British Journal of Nutrition, 98(1), 45-53. https://doi.org/10.1017/S0007114507472506
  38. Skrypnik, L., Feduraev, P., Styran, T., Golovin, A., Katserov, D., Nebreeva, S., & Maslennikov, P. (2022). Biomass, phenolic compounds, essential oil content, and antioxidant properties of Hyssop (Hyssopus officinalis) grown in hydroponics as affected by treatment type and selenium concentration. Horticulturae, 8(11), 1037. https://doi.org/10.3390/horticulturae8111037
  39. Theodorou, M.K., Williams, B.A., Dhanoa, M.S., McAllan, A.B., & France, J. (1994). A simple gas production method using a pressure transducer to determine the fermentation kinetics of ruminant feed. Animal Feed Science and Technology, 48(3-4), 185-197. https://doi.org/10.1016/0377-8401(94)90171-6
  40. Van Soest, P.V., Robertson, J.B., & Lewis, B.A. (1991). Methods for dietary fiber, neutral detergent fiber, and nonstarch polysaccharides in relation to animal nutrition. Journal of Dairy Science, 74(10), 3583-3597. https://doi.org/10.3168/jds.S0022-0302(91)78551-2
  41. Vercoe, E.P., Makkar, H.P.S., & Schlink, A.C. (2010). In vitro screening of plant resources for extra nutritional attributes in ruminants: Nuclear and related methodologies. In: In vitro screening of feed resources for efficiency of microbial protein synthesis. Springer, New York, pp. 106-144. https://doi.org/10.1007/978-90-481-3297-3
  42. Wencelová, M., Váradyová, Z., Mihaliková, K., Čobanová, K., Plachá, I., Pristaš, P., Jalč, D., & Kišidayová, S. (2015). Rumen fermentation pattern, lipid metabolism and the microbial community of sheep fed a high-concentrate diet supplemented with a mix of medicinal plants. Small Ruminant Research, 125: 64-72. https://doi.org/10.1016/j.smallrumres.2015.01.028
  43. Yousefi, M., Hoseini, S.M., Abtahi, B., Vatnikov, Y.A., Kulikov, E.V., & Rodionova, N.Y. (2022). Effects of dietary methanolic extract of hyssop, Hyssopus officinalis, on growth performance, hepatic antioxidant, humoral and intestinal immunity, and intestinal bacteria of rainbow trout, Oncorhynchus mykiss. Frontiers in Marine Science, 9: https://doi.org/10.3389/fmars.2022.1026651
  44. Zheng, S., Li, Y., Chen, C., Wang, N., & Yang, F. (2025). Solutions to the dilemma of antibiotics use in livestock and poultry farming: Regulation policy and alternatives. Toxics, 13(5), 348. https://doi.org/10.3390/toxics13050348  
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