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Wang, L.;  Gao, H.;  Sun, C.;  Huang, L. Nutrients and Bioactive Compounds in the Mulberry. Encyclopedia. Available online: https://encyclopedia.pub/entry/38980 (accessed on 05 December 2025).
Wang L,  Gao H,  Sun C,  Huang L. Nutrients and Bioactive Compounds in the Mulberry. Encyclopedia. Available at: https://encyclopedia.pub/entry/38980. Accessed December 05, 2025.
Wang, Lixue, Huaqi Gao, Cui Sun, Lingxia Huang. "Nutrients and Bioactive Compounds in the Mulberry" Encyclopedia, https://encyclopedia.pub/entry/38980 (accessed December 05, 2025).
Wang, L.,  Gao, H.,  Sun, C., & Huang, L. (2022, December 20). Nutrients and Bioactive Compounds in the Mulberry. In Encyclopedia. https://encyclopedia.pub/entry/38980
Wang, Lixue, et al. "Nutrients and Bioactive Compounds in the Mulberry." Encyclopedia. Web. 20 December, 2022.
Nutrients and Bioactive Compounds in the Mulberry
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The mulberry tree belongs to the Morus genus of the Moraceae family, and is distributed all over the world. The mulberry tree contains 24 species and one subspecies.

mulberry extracts animal production active compounds

1. Introduction

Population growth, urbanization, and rising incomes have led to the dramatic demand for animal products [1]. The global demand for animal products will rise by more than two-thirds by the year 2050 [2]. With the increasing demand for animal products, we have to explore new non-conventional feed resources to ensure the sustainability of animal production [3][4]. A variety of alternative feed resources exist for livestock, such as crop residues, the leaves of shrubs and trees, and weeds. However, these alternative feed resources have a lower digestibility, a lower content of protein and energy, and higher antinutritional factors, which limit their application [5][6].
The mulberry tree belongs to the Morus genus of the Moraceae family, and is distributed all over the world [7]. The mulberry tree contains 24 species and one subspecies. Among them, M. albus, M. atropurpurea, M. multicaulis, and M. bombycis are the dominant species [8]. The mulberry tree originated in China, Japan, and the Himalayan foothills. China possesses the most mulberry land with over 626,000 ha, followed by India with around 280,000 ha [9].
The mulberry tree is rich in bioactive compounds, including polysaccharides, phenols, flavonoids, and alkaloids, and has been reported to possess potent beneficial properties, including antioxidative, antidiabetic, and anti-cholesterol [10]. All parts of the mulberry tree, including the leaves, fruits, stems, and roots, are used for various purposes [11]. In addition, mulberry leaves are an excellent source of protein for livestock, with 14.0–34.2% protein content [12][13]. Extensive studies have demonstrated that mulberry leaves are a high quality protein source in the diets of animals, including pigs [14], hens [15], sheep [16], and cattle [17]. However, the effects of the mulberry tree and its extracts on animals are dependent on several factors, such as animal species, level of supplementation, the method for using the mulberry, and farm management. Individual studies cannot take into account all of these variables.

2. Nutrients Derived from the Mulberry Tree and Its Extracts

The mulberry tree, a member of the family Moraceae and genus Morus [18], is widely distributed throughout the world [19]. Morus alba (white mulberry), Morus nigra (black mulberry), and Morus rubra (red mulberry) are the most common species [20]. The mulberry tree is a potential protein source for animals. Different parts of the mulberry, especially the leaves and fruits, contain a variety of nutrients [21].

2.1. Leaves

The nutritional composition of the mulberry leaves is influenced by many factors, such as the varieties, environments, ecologies, and harvest conditions, and the nutritional composition varies greatly in different studies. All of the reported nutrient components in the mulberry leaves are displayed in Table 1. Fresh mulberry leaves contain dry matter (DM, 19.8–30.40%), a substantial amount of crude protein (CP, 4.72–22.3%), fats (0.64–4.36%), crude fiber (CF, 5.26–15.9%), total ash (4.10–14.50%), carbohydrates (carb, 8.01–13.42%), neutral detergent fiber (NDF, 8.15–43.4%), and gross energy (GE, 69–224 kcal/100 g) [22][23][24][25][26]. Moreover, according to Srivastava et al. [22], mulberry leaves are a plentiful source of important minerals and vitamins, such as calcium (Ca, 380–786 mg/100 g), ascorbic acid (200–280 mg/100 g), β-carotene (10,000–14,688 μg/100 g), iron (Fe, 4.7–10.36 mg/100 g), zinc (Zn, 0.22–1.12 mg/100 g), and tannic acid (0.04–0.08%).
As for dried mulberry leaves powder, it contains DM (18.0–95.5%), CP (11.75–37.36%), fats (2–11.10%), CF (5.4–32.3%), nitrogen free extract (NFE, 42.2–54%), NDF (19.38–36.66%), acid detergent fiber (ADF, 10.2–29.7%), total ash (7.56–22.36%), carb (9.7–56.42%), and GE (113–422 kcal/100 g) [22][25][27][28][29][30][31][32][33][34][35][36][37][38]. Dried mulberry leaves powder also possesses Ca (137.5–2226 mg/100 g), ascorbic acid (100–200 mg/100 g), β-carotene (8438–13,125 μg/100 g), Fe (14.15–35.72 mg/100 g), Zn (0.72–5.75 mg/100 g), and tannic acid (0.12–0.76%) [22][27][31][32][36].
Table 1. Chemical composition of mulberry leaves.

2.2. Fruits

The mulberry fruit also contains CP, fats, minerals, and other components, and is a healthy food choice for consumers [39]. Similar to mulberry leaves, the nutritional and chemical composition of the mulberry fruit changes with the varieties, environments, climatic conditions, and soil conditions. The average contents of the trace element components in the mulberry fruits are shown in Table 2. DM can range from 9.45% to 28.50%, CP can vary from 0.51% to 12.98%, fat can vary from 0.34% to 7.21%, CF can vary from 0.57% to 14.0%, ash can vary from 0.46% to 4.79%, and carb can vary from 13.83% to 71.7% [20][40][41][42][43][44][45][46]. A study by Imran et al. [41] showed that the GE in the mulberry fruit can range from 67.36 to 84.22 kcal/100 g.
Table 2. Trace element composition of the mulberry fruits (mg/100 g).
Additionally, the mulberry fruit also contains Fe (1.17–77.6 mg/100 g), Zn (0.14–59.20 mg/100 g), Ca (38.89–576 mg/100 g), magnesium (Mg, 12.21–360 mg/100 g), kalium (K, 87.70–2170 mg/100 g), sodium (Na, 5.9–280 mg/100 g), manganese (Mn, 0.03–4.36 mg/100 g), and copper (Cu, 0.04–1.31%) [20][40][41][42][43][46][47][48][49]. Ascorbic acid ranges from 15.20 to 22.4 mg/100 g [20][41]
Collectively, the chemical composition of mulberry leaves and mulberry fruits varies greatly due to the different varieties, geographical environment, seasons, and other factors. The results suggest that researchers should pay attention to the regional and variety differences of the mulberry tree’s raw materials, when using mulberry tree products in feed production.

3. Bioactive Compounds in the Mulberry and Their Bioactivities

The history of the mulberry tree and its extracts used as a medicinal herb is very long, due to its extensive biological and pharmacological activities [50]. Mulberry plants contain a variety of compounds with medical and veterinary pharmacological properties, including alkaloids, flavonoids, phenolic acids, and others. These compounds have antioxidant, anti-inflammatory, antibacterial, anticancer, antidiabetic, neuroprotective, cardioprotective, hepatoprotective, antihypertensive, anti-apoptosis, antiviral, anti-arteriosclerosis, and antidepressant properties (Figure 1).
Figure 1. Main mulberry components and their bioactivities.
The mulberry tree is identified as an appreciable source of flavonoids, which have beneficial effects on human and animal health. Previous studies reported that the concentrations of the total flavonoids were 9.84–58.42 mg/g in dried mulberry leaves from different varieties [33][35][51][52]. Flavonoids have been reported to exert diverse biological effects, such as anticancer, neuroprotective, hepatoprotective, nephroprotective, antidiabetic, cardio-protection, and antibacterial, mainly associated with their antioxidant and anti-inflammatory activities [53][54]. Further studies showed that the inflammatory and antioxidant effects of flavonoids were mediated through regulating the NF-κB, AP-1, PPAR, Nrf2, MAPKs, JNK, p38, ERK, PI3-K/Akt, and PKC signaling pathways [55][56].
1-Deoxynojirimycin (1-DNJ), a polyhydroxylated piperidine alkaloid [35], is a potent α-glucosidase inhibitor with unique bioactivities, such as anti-inflammatory, antioxidant, and anticancer [57][58][59]. 1-DNJ exhibited anti-hyperglycemic activity through regulating the expression of proteins related to glucose transport systems, glycolysis, and gluconeogenesis enzymes [60][61][62]. In addition, 1-DNJ also possesses anti-microbial properties. Hu et al. [61] reported that the 1-DNJ treatment could promote the growth of beneficial bacteria and suppress the growth of harmful bacteria in a streptozotocin-induced diabetic mouse model.
Phenolic acids were found to be excellent antioxidant agents. By scavenging free radicals, modulating the antioxidant enzyme activity, and regulating the signaling pathways associated with oxidative stress, the phenolic acids can exert an antioxidant activity [63][64]. Phenolic acids are also known for their anti-inflammatory properties. Oxidative stress and the resulting oxidative damage play an important role in the formation and progression of cancer [65]. To some extent, phenolic acids could inhibit the proliferation of colon cancer cells and induce apoptosis in cancer cells through oxidant-mediated mechanisms [66]. Previous studies demonstrated that phenolic acids could rupture the cell membrane integrity and inhibit the growth of pathogenic bacteria [67][68][69]. The significant antidiabetic effect of phenolic acids may be due to the reduced levels of oxidative stress and pro-inflammatory cytokines [70][71]. Peng et al. [72] found that phenolic acids maintain the glucose homeostasis by regulating the expression of the intestinal glucose transporters and proglucagon.

References

  1. Thornton, P.K. Livestock production: Recent trends, future prospects. Philos. Trans. R. Soc. B Biol. Sci. 2010, 365, 2853–2867.
  2. FAO. Transforming the livestock sector through the sustainable development goals; World Livestock: Rome, Italy, 2018.
  3. Rauw, W.M.; Rydhmer, L.; Kyriazakis, I.; Øverland, M.; Gilbert, H.; Dekkers, J.C.; Hermesch, S.; Bouquet, A.; Gómez Izquierdo, E.; Louveau, I.; et al. Prospects for sustainability of pig production in relation to climate change and novel feed resources. J. Sci. Food Agric. 2020, 100, 3575–3586.
  4. Ponnampalam, E.N.; Holman, B.W.B. Chapter 22—Sustainability II: Sustainable animal production and meat processing. In Lawrie’s Meat Science (Ninth Edition); Toldrá, F., Ed.; Woodhead Publishing: Sawston, UK, 2023; pp. 727–798.
  5. Abadi, N.A. Major non-conventional feed resources of livestock. Int. J. Eng. Dev. Res. 2018, 6, 786–789.
  6. Torma, S.; Vilček, J.; Lošák, T.; Kužel, S.; Martensson, A. Residual plant nutrients in crop residues—An important resource. Acta Agric. Scand. Sect. B—Soil Plant Sci. 2017, 68, 358–366.
  7. Machii, H.; Koyama, A.; Yamanouchi, H. Mulberry breeding, cultivation and utilization in Japan. FAO Anim. Prod. Health Pap. 2000, 147, 63.
  8. Huo, Y. Mulberry cultivation and utilization in China. FAO Anim. Prod. Health Pap. 2000, 1, 11–44.
  9. Sánchez, M.D. World distribution and utilization of mulberry, potential for animal feeding. FAO Anim. Prod. Health Pap. 2000, 111, 1–11.
  10. Wen, P.; Hu, T.G.; Linhardt, R.J.; Liao, S.T.; Wu, H.; Zou, Y.X. Mulberry: A review of bioactive compounds and advanced processing technology. Trends Food Sci. Technol. 2019, 83, 138–158.
  11. Jan, B.; Parveen, R.; Zahiruddin, S.; Khan, M.U.; Mohapatra, S.; Ahmad, S. Nutritional constituents of mulberry and their potential applications in food and pharmaceuticals: A review. Saudi J. Biol. Sci. 2021, 28, 3909–3921.
  12. Ba, N.X.; Giang, V.D.; NgoanJan, L.D. Ensiling of mulberry foliage (Morus alba) and the nutritive value of mulberry foliage silage for goats in central Vietnam. Livest. Res. Rural. Dev. 2005, 17, 23–25.
  13. Simbaya, J.; Chibinga, O.; Salem, A.Z.M. Nutritional evaluation of selected fodder trees: Mulberry (Molus alba Lam.), Leucaena (Leucaena luecocephala Lam de Wit.) and Moringa (Moringa oleifera Lam.) as dry season protein supplements for grazing animals. Agrofor. Syst. 2020, 94, 1189–1197.
  14. Liu, Y.Y.; Li, Y.H.; Peng, Y.L.; He, J.H.; Xiao, D.F.; Chen, C.; Li, F.N.; Huang, R.L.; Yin, Y.L. Dietary mulberry leaf powder affects growth performance, carcass traits and meat quality in finishing pigs. J. Anim. Physiol. Anim. Nutr. 2019, 103, 1934–1945.
  15. Al-kirshi, R.; Alimon, A.; Idrus, Z.; Mohamed, W.Z.; Michel, I. Utilization of mulberry leaf meal (Morus alba) as protein supplement in diets for laying hens. Ital. J. Anim. Sci. 2010, 9, 265–267.
  16. Mengistu, G.; Assefa, G.; Tilahun, S. Noug seed (Guizotia abyssinica) cake substituted with dried mulberry (Morus indica) and Vernonia amygdalina mixed leaves’ meal on growth performances of Bonga Sheep at Teppi, Ethiopia. J. Nutr. Metab. 2020, 2020, 9308761.
  17. Cheong, S.H.; Kim, K.H.; Jeon, B.; Park, P.J.; Hwang, I.; Choi, N.; Kim, E.; Hong, S.; Park, J.; Sung, S.; et al. Effect of mulberry silage supplementation during late fattening stage of Hanwoo (Bos taurus coreanae) steer on antioxidative enzyme activity within the longissimus muscle. Anim. Prod. Sci. 2012, 52, 240–247.
  18. Zhang, S.D.; Soltis, D.E.; Yang, Y.; Li, D.Z.; Yi, T.S. Multi-gene analysis provides a well-supported phylogeny of Rosales. Mol. Phylogenetics Evol. 2011, 60, 21–28.
  19. Tutin, G.T.; Morus, L. Psilotaceae to Platanaceae; Cambridge University Press: Melbourne VIC, Australia, 1996.
  20. Ercisli, S.; Orhan, E. Chemical composition of white (Morus alba), red (Morus rubra) and black (Morus nigra) mulberry fruits. Food Chem. 2007, 103, 1380–1384.
  21. Chauhan, S.; Kumar, R. Biochemical constituents of different parts of mulberry genotypes. Int. J. Agric. Sci. 2011, 3, 90–96.
  22. Srivastava, S.; Kapoor, R.; Thathola, A.; Srivastava, R.P. Nutritional quality of leaves of some genotypes of mulberry (Morus alba). Int. J. Food Sci. Nutr. 2006, 57, 305–313.
  23. Todaro, M.; Bonanno, A.; Tornambè, G.; Di Grigoli, A.; Luisa Scatassa, M.; Giaccone, P. Utilization of mulberry leaves (Morus latifolia cv. Kokusou 21) in diets for dairy ewes. Ital. J. Anim. Sci. 2009, 8, 438–440.
  24. Vu, C.C.; Verstegen, M.W.A.; Hendriks, W.H.; Pham, K. The Nutritive value of mulberry leaves (Morus Alba) and partial replacement of cottonseed in rations on the performance of growing Vietnamese cattle. Asian Australas. J. Anim. Sci. 2011, 24, 1233–1242.
  25. Dolis, M.G.; Simeanu, C.; Usturoi, A.; Simeanu, D. Research regarding chemical composition and the digestibility of the mulberry leaves from eforie variety. Rev. De Chim. 2017, 68, 151–156.
  26. Yao, J.; Yan, B.; Wang, X.Q.; Liu, J.X. Nutritional evaluation of mulberry leaves as feeds for ruminants. Livest. Res. Rural. Dev. 2000, 12, 9–16.
  27. Adeduntan, S.; Oyerinde, A. Evaluation of chemical and antinutritional characteristics of obeche (Triplochition scleroxylon) and some mulberry (Morus alba) leaves. Int. J. Biol. Chem. Sci. 2009, 3, 681–687.
  28. Kandylis, K.; Hadjigeorgiou, I.; Harizanis, P. The nutritive value of mulberry leaves (Morus alba) as a feed supplement for sheep. Trop. Anim. Health Prod. 2009, 41, 17–24.
  29. Al-kirshi, R.; Alimon, A.; Zulkifli, R.; Sazili, I.; Zahari, A. The chemical composition and nutritive value of mulberry leaf meal as a protein source in poultry diets. In International Seminar on Animal Industry; Atlantis Press: Amsterdam, The Netherlands, 2009.
  30. Sahoo, A.; Singh, B.; Sharma, O.P. Evaluation of feeding value of Eupatorium adenophorum in combination with mulberry leaves. Livest. Sci. 2011, 136, 175–183.
  31. Guven, I. Effect of species on nutritive value of mulberry leaves. Kafkas Univ. Veter Fak. Derg. 2012, 18, 865–869.
  32. Wang, W.X.; Yang, H.J.; Bo, Y.K.; Ding, S.; Cao, B.H. Nutrient composition, polyphenolic contents, and in situ protein degradation kinetics of leaves from three mulberry species. Livest. Sci. 2012, 146, 203–206.
  33. Iqbal, S.; Younas, U.; Sirajuddin; Chan, K.W.; Sarfraz, R.A.; Uddin, K. Proximate composition and antioxidant potential of leaves from three varieties of mulberry (Morus sp.): A comparative study. Int. J. Mol. Sci. 2012, 13, 6651–6664.
  34. Flaczyk, E.; Kobus-Cisowska, J.; Przeor, M.; Korczak, J.; Remiszewski, M.; Korbas, E.; Buchowski, M. Chemical characterization and antioxidative properties of polish variety of Morus alba L. leaf aqueous extracts from the laboratory and pilot-scale processes. Agric. Sci. 2013, 4, 141–147.
  35. Yu, Y.; Li, H.; Zhang, B.; Wang, J.; Shi, X.; Huang, J.; Yang, J.; Zhang, Y.; Deng, Z. Nutritional and functional components of mulberry leaves from different varieties: Evaluation of their potential as food materials. Int. J. Food Prop. 2018, 21, 1495–1507.
  36. Cai, M.; Mu, L.; Wang, Z.L.; Liu, J.Y.; Liu, T.L.; Wanapat, M.; Huang, B.Z. Assessment of mulberry leaf as a potential feed supplement for animal feeding in P.R. China. Asian Australas. J. Anim. Sci. 2019, 32, 1145–1152.
  37. Kang, J.; Wang, R.; Tang, S.; Wang, M.; Tan, Z.; Bernard, L.A. Chemical composition and in vitro ruminal fermentation of pigeonpea and mulberry leaves. Agrofor. Syst. 2020, 94, 1521–1528.
  38. Ouyang, J.; Wang, M.; Hou, Q.; Feng, D.; Pi, Y.; Zhao, W. Effects of dietary mulberry leaf powder in concentrate on the rumen fermentation and ruminal epithelium in Fattening Hu Sheep. Animals 2019, 9, 218.
  39. Manzoor, M.F.; Hussain, A.; Tazeddinova, D.; Abylgazinova, A.; Xu, B. Assessing the nutritional-value-based therapeutic potentials and non-destructive approaches for mulberry fruit assessment: An overview. Comput. Intell. Neurosci. 2022, 2022, 6531483–6531499.
  40. Koca, I.; Ustun, S.; Koca, A.; Karadeniz, B. Chemical composition, antioxidant activity and anthocyanin profiles of purple mulberry (Morus rubra) fruits. J. Food Agric. Environ. 2008, 6, 39–42.
  41. Imran, M.; Khan, H.; Shah, M.; Khan, R.; Khan, F. Chemical composition and antioxidant activity of certain Morus species. J. Zhejiang Univ. Sci. B 2010, 11, 973–980.
  42. Sánchez-Salcedo, E.M.; Mena, P.; García-Viguera, C.; Martínez, J.J.; Hernández, F. Phytochemical evaluation of white (Morus alba L.) and black (Morus nigra L.) mulberry fruits, a starting point for the assessment of their beneficial properties. J. Funct. Foods 2015, 12, 399–408.
  43. Jiang, Y.; Nie, W.J. Chemical properties in fruits of mulberry species from the Xinjiang province of China. Food Chem. 2015, 174, 460–466.
  44. Owon, M.A.; Gafar, A.M.; Saleh, S.M.; Shaheen, M.M. Identification of bioactive compounds from egyptian mulberry fruits and their uses in improvement the quality of some foods. J. Sustain. Agric. Sci. 2016, 42, 33–52.
  45. Munir, A.; Khera, R.A.; Rehman, R.; Nisar, S. Multipurpose white mulberry: A review. Int. J. Biol. Chem. Sci. 2018, 13, 31–35.
  46. Sun, R.; Sun, L.; Han, C. Partial-least-squares and canonical-correlation analysis of chemical constituents and active ingredients of new types of Chinese mulberries. Food Sci. Nutr. 2018, 6, 1950–1959.
  47. Akbulut, M.; Ozcan, M.M. Comparison of mineral contents of mulberry (Morus spp.) fruits and their pekmez (boiled mulberry juice) samples. Int. J. Food Sci. Nutr. 2009, 60, 231–239.
  48. Sheng, J.P.; Liu, C.; Shen, L. Analysis of 14 minerals of mulberry fruit in different mature stage by ICP-OES method. Spectscopy Spectr. Anal. 2009, 29, 2574–2576.
  49. Altundag, H.; Tuzen, M. Comparison of dry, wet and microwave digestion methods for the multi element determination in some dried fruit samples by ICP-OES. Food Chem. Toxicol. 2011, 49, 2800–2807.
  50. Kadam, R.; Dhumal, N.; Khyade, V. The mulberry, Morus alba (L.): The medicinal herbal source for human health. Int. J. Curr. Microbiol. Appl. Sci. 2019, 8, 2941–2964.
  51. Zhishen, J.; Mengcheng, T.; Jianming, W. The determination of flavonoid contents in mulberry and their scavenging effects on superoxide radicals. Food Chem. 1999, 64, 555–559.
  52. He, X.Y.; Chen, X.; Ou, X.Q.; Ma, L.Y.; Xu, W.T.; Huang, K.L. Evaluation of flavonoid and polyphenol constituents in mulberry leaves using HPLC fingerprint analysis. Int. J. Food Sci. Technol. 2020, 55, 526–533.
  53. Saxena, M.; Saxena, J.; Pradhan, A. Flavonoids and phenolic acids as antioxidants in plants and human health. Int. J. Pharm. Sci. Res. 2012, 16, 130–134.
  54. Maleki, S.J.; Crespo, J.F.; Cabanillas, B. Anti-inflammatory effects of flavonoids. Food Chem. 2019, 299, 125124.
  55. Chen, L.; Teng, H.; Jia, Z.; Battino, M.; Miron, A.; Yu, Z.; Cao, H.; Xiao, J. Intracellular signaling pathways of inflammation modulated by dietary flavonoids: The most recent evidence. Crit. Rev. Food Sci. Nutr. 2018, 58, 2908–2924.
  56. Mansuri, M.L.; Parihar, P.; Solanki, I.; Parihar, M.S. Flavonoids in modulation of cell survival signalling pathways. Genes Nutr. 2014, 9, 400.
  57. Li, A.N.; Chen, J.J.; Li, Q.Q.; Zeng, G.Y.; Chen, Q.Y.; Chen, J.L.; Liao, Z.M.; Jin, P.; Wang, K.S.; Yang, Z.C. Alpha-glucosidase inhibitor 1-Deoxynojirimycin promotes beige remodeling of 3T3-L1 preadipocytes via activating AMPK. Biochem. Biophys. Res. Commun. 2019, 509, 1001–1007.
  58. Hu, X.Q.; Thakur, K.; Chen, G.H.; Hu, F.; Zhang, J.G.; Zhang, H.B.; Wei, Z.J. Metabolic effect of 1-deoxynojirimycin from mulberry leaves on db/db diabetic mice using liquid chromatography-mass spectrometry based metabolomics. J. Agric. Food Chem. 2017, 65, 4658–4667.
  59. Piao, X.H.; Li, S.D.; Sui, X.D.; Guo, L.Y.; Liu, X.M.; Li, H.M.; Gao, L.M.; Cai, S.S.; Li, Y.R.; Wang, T.T.; et al. 1-Deoxynojirimycin (DNJ) ameliorates indomethacin-induced gastric ulcer in mice by affecting NF-kappaB signaling pathway. Front. Pharmacol. 2018, 9, 372.
  60. Li, Q.; Wang, Y.; Dai, Y.; Shen, W.; Liao, S.; Zou, Y. 1-Deoxynojirimycin modulates glucose homeostasis by regulating the combination of IR-GlUT4 and ADIPO-GLUT4 pathways in 3T3-L1 adipocytes. Mol. Biol. Rep. 2019, 46, 6277–6285.
  61. Hu, T.G.; Wen, P.; Shen, W.Z.; Liu, F.; Li, Q.; Li, E.N.; Liao, S.T.; Wu, H.; Zou, Y.X. Effect of 1-Deoxynojirimycin isolated from mulberry leaves on glucose metabolism and gut microbiota in a streptozotocin-induced diabetic mouse model. J. Nat. Prod. 2019, 82, 2189–2200.
  62. Parida, I.S.; Takasu, S.; Ito, J.; Ikeda, R.; Yamagishi, K.; Kimura, T.; Eitsuka, T.; Nakagawa, K. Supplementation of Bacillus amyloliquefaciens AS385 culture broth powder containing 1-deoxynojirimycin in high-fat diet altered the gene expressions related to lipid metabolism and insulin signaling in mice epididymal white adipose tissue. Food Funct. 2020, 11, 3926–3940.
  63. Mathew, N.S.; Negi, P.S. Phenolic content and anti-oxidative attributes of various parts of wild banana (Ensete superbum Roxb. Cheesman) plant. J. Food Biochem. 2021, 45, e13657.
  64. Yahfoufi, N.; Alsadi, N.; Jambi, M.; Matar, C. The immunomodulatory and anti-inflammatory role of polyphenols. Nutrients 2018, 10, 1618.
  65. Klaunig, J.E. Oxidative stress and cancer. Curr. Pharm. Des. 2018, 24, 4771–4778.
  66. Rosa, L.; Nja, S. Anticancer properties of phenolic acids in colon cancer—A review. J. Nutr. Food Sci. 2016, 6, 1000468.
  67. Qian, W.D.; Yang, M.; Wang, T.; Sun, Z.H.; Liu, M.; Zhang, J.N.; Zeng, Q.; Cai, C.L.; Li, Y.D. Antibacterial mechanism of vanillic acid on physiological, morphological, and biofilm properties of carbapenem-resistant enterobacter hormaechei. J. Food Prot. 2020, 83, 576–583.
  68. Yan, Y.W.; Zhou, X.; Guo, K.X.; Zhou, F.; Yang, H.Q. Chlorogenic acid protects against indomethacin-induced inflammation and mucosa damage by decreasing Bacteroides-derived LPS. Front. Immunol. 2020, 11, 1125.
  69. Zeng, J.H.; Wan, X.Y.; Liu, T.; Xiong, Y.; Xiang, G.; Peng, Y.L.; Zhu, R.H.; Zhou, Y.Q.; Liu, C.Q. Chlorogenic acid ameliorates Klebsiella pneumoniae-induced pneumonia in immunosuppressed mice via inhibiting the activation of NLRP3 inflammasomes. Food Funct. 2021, 12, 9466–9475.
  70. Saraswat, N.; Sachan, N.; Chandra, P. Anti-diabetic, diabetic neuropathy protective action and mechanism of action involving oxidative pathway of chlorogenic acid isolated from Selinum vaginatum roots in rats. Heliyon 2020, 6, e05137.
  71. Qin, L.H.; Zang, M.X.; Xu, Y.; Zhao, R.R.; Wang, Y.T.; Mi, Y.; Mei, Y.W. Chlorogenic acid alleviates hyperglycemia-induced cardiac fibrosis through activation of the NO/cGMP/PKG pathway in cardiac fibroblasts. Mol. Nutr. Food Res. 2021, 65, e2000810.
  72. Peng, B.J.; Zhu, Q.; Zhong, Y.L.; Xu, S.H.; Wang, Z. Chlorogenic acid maintains glucose homeostasis through modulating the expression of SGLT-1, GLUT-2, and PLG in different intestinal segments of sprague-dawley rats fed a high-fat diet. Biomed. Environ. Sci. 2015, 28, 894–903.
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