Abstract
Deer antler velvet, with kidney tonifying, promoting the production of essence and blood, strengthening tendons and bones, not only has a thousand-year medicinal history but also its modern pharmacology mainly focuses on its active polypeptides on motor, nerve, and immune systems. The purpose of this report is to fill the gap in the comprehensive, systematic, and detailed review of polypeptides during the recent 30 years (1992–2023). The research method was to review 53 pharmacological articles from the Public Medicine, Web of science, ACS, and Science Direct database sources by searching the keywords “pilose antler,” “deer velvet,” “Pilose Antler Peptide (PAP) and Velvet Antler Polypeptide (VAP).” The results showed that deer antler polypeptides (DAPs), by regulating EGF, EGFR, MAPK, P38, ERK, NF-κB, Wnt, PI3K, Akt, MMP, AMPK, Stir1, NLRP3, HO-1, Nrf, Rho, TLR, TGF-β, Smad, Ang II, etc., revealed their effects on seven system-related diseases and their mechanisms, including osteoarthritis, intervertebral disc degeneration, osteoporosis, Alzheimer’s, Parkinson’s, triple-negative breast cancer, liver injury, liver fibrosis, cardiovascular disease, acute lung injury, and late-onset hypogonadism. In conclusion, DAPs have good effects on motor and other system-related diseases, but the secondary and tertiary structures of DAPs (0.5–1800 KDa) need to be further elucidated, and the structure–activity relationship study is still unavailable and needs to be covered. It is expected that this review may provide the necessary literature support for further research.
Graphical Abstract
The activities and mechanisms of polypeptides from the past 30 years (1992–2023) are summarized covering seven systems, related diseases, and its regulatory genes and proteins.
Similar content being viewed by others
Data availability
Not applicable.
References
Abdel-Rasoul AA, Saleh NA, Hosny EN, El-Gizawy MM, Ibrahim EA (2023) Cardamom oil ameliorates behavioral and neuropathological disorders in a rat model of depression induced by reserpine. J Ethnopharmacol 308:116254. https://doi.org/10.1016/j.jep.2023.116254
Aggarwal R, Bains K (2022) Protein, lysine and vitamin D: critical role in muscle and bone health. Crit Rev Food Sci Nutr 62(9):2548–2559. https://doi.org/10.1080/10408398.2020.1855101
Bai L, Shi W, Liu J, Zhao X, Zhang Y, Zhou Z, Hou W, Chang T (2017) Protective effect of pilose antler peptide on cerebral ischemia/reperfusion (I/R) injury through Nrf-2/OH-1/NF-κB pathway. Int J Biol Macromol 102:741–748. https://doi.org/10.1016/j.ijbiomac.2017.04.091
Bo SR, Yu JH, Wang YL, Wang QK (2017) Preparation and antimicrobial activity of antimicrobial peptides from plum deer antler. Atlantis Press 141:787–792
Carlsson E, Cowell-McGlory T, Hedrich CM (2023) cAMP responsive element modulator α promotes effector T cells in systemic autoimmune diseases. Immunology. https://doi.org/10.1111/imm.13680.10.1111/imm.13680
Chen X, Chen D, Ban E, Toussaint KC, Janmey PA, Wells RG, Shenoy VB (2022) Glycosaminoglycans modulate long-range mechanical communication between cells in collagen networks. Proc Nat Acad Sci U S A 119(15):e2116718119. https://doi.org/10.1073/pnas.2116718119
Chunhua M, Hongyan L (2017) Protective effect of pilose antler peptide on carbon tetrachloride-induced hepatotoxicity in mice. Int J Biol Macromol 99:648–654. https://doi.org/10.1016/j.ijbiomac.2017.03.024
Chunhui Y, Wenjun C, Hui W, Liquan S, Changwei Z, Tianzhu Z, Wenhai Z (2017) Pilose antler peptide protects osteoblasts from inflammatory and oxidative injury through EGF/EGFR signaling. Int J Biol Macromol 99:15–20. https://doi.org/10.1016/j.ijbiomac.2017.02.056
Ding Y, Ko SC, Moon SH, Lee SH (2019) Protective effects of novel antioxidant peptide purified from alcalase hydrolysate of velvet antler against oxidative stress in chang liver cells in vitro and in a zebrafish model in vivo. Int J Mol Sci 20:5187. https://doi.org/10.3390/ijms20205187
Dong Y, Liu L, Shan X, Tang J, Xia B, Cheng X, Chen Y, Tao W (2018) Pilose antler peptide attenuates LPS-induced inflammatory reaction. Int J Biol Macromol 108:272–276. https://doi.org/10.1016/j.ijbiomac.2017.11.176
Duan LX, Wang C, Xin JL, Duan YM, Wang JG (2015) Therapeutic effects of velvet antler polypetides on hepatic fibrosis in rats. Chin J/phormacol/toxicol 29:56–57
Feng L, Wang Y, Yang J, Sun YF, Li YW, Ye ZH, Lin HB, Yang K (2022) Overview of the preparation method, structure and function, and application of natural peptides and polypeptides. Biomed Pharmacother 153:113493. https://doi.org/10.1016/j.biopha.2022.113493
Galoian K, Dahl V, Perez A, Denny C, Becker B, Sedani A, Moran A, Martinez D, Hoyt A, Brown J (2022) PRP-1, a toll-like receptor ligand, upregulates the unfolded protein response in human chondrosarcoma cells. Cancer Treat Res Commun 33:100644. https://doi.org/10.1016/j.ctarc.2022.100644
Gavva C, Patel K, Kudre T, Sharan K, Chilkunda DN (2020) Glycosaminoglycans from fresh water fish processing discard - isolation, structural characterization, and osteogenic activity. Int J Biol Macromol 145:558–567. https://doi.org/10.1016/j.ijbiomac.2019.12.189
Grahnemo L, Eriksson AL, Nethander M, Johansson R, Lorentzon M, Mellström D, Pettersson-Kymmer U, Ohlsson C (2023) Low circulating valine associate with high risk of hip fractures. J Clin Endocrinol Metab dgad268. https://doi.org/10.1210/clinem/dgad268
Gronthos S, Zannettino AC, Hay SJ, Shi S, Graves SE, Kortesidis A, Simmons PJ (2003) Molecular and cellular characterisation of highly purified stromal stem cells derived from human bone marrow. J Cell Sci 116:1827–1835. https://doi.org/10.1242/jcs.00369
Guan SW, Duan LX, Li YY, Wang BX, Zhou QL (2006) A novel polypeptide from Cervus nippon Temminck proliferation of epidermal cells and NIH3T3 cell line. Acta Biochim Pol 53:395–397
Guo J, Lu M, Zhou Y, Wu B, Wu M (2020) Effects of velvet antler polypeptides on Alzheimer’s disease cell model via miR-613 HDAC6 pathway. Pak J Pharm Sci 33:1427–1433
Hammoutene A, Rautou PE (2019) Role of liver sinusoidal endothelial cells in non-alcoholic fatty liver disease. J Hepatol 70:1278–1291. https://doi.org/10.1016/j.jhep.2019.02.012
Hu Y, Zhao M, Zhao T, Qi M, Yao G, Dong Y (2022) The protective effect of pilose antler peptide on CUMS-induced depression through AMPK/Sirt1/NF-κB/NLRP3-mediated pyroptosis. Front Pharmacol 13:815413. https://doi.org/10.3389/fphar.2022.815413
Hu X, Ge Q, Zhang Y, Li B, Cheng E, Wang Y, Huang Y (2023) A review of the effect of exosomes from different cells on liver fibrosis. Biomed Pharmacother 161:114415. https://doi.org/10.1016/j.biopha.2023.114415
Iseri VJ, Klasing KC (2014) Changes in the amount of lysine in protective proteins and immune cells after a systemic response to dead Escherichia coli: implications for the nutritional costs of immunity. Integr Comp Biol 54(5):922–930. https://doi.org/10.1093/icb/icu111
Jiang W, Zhang J, Zhang X, Fan C, Huang J (2021) VAP-PLGA microspheres (VAP-PLGA) promote adipose-derived stem cells (ADSCs)-induced wound healing in chronic skin ulcers in mice via PI3K/Akt/HIF-1α pathway. Bioengineered 12:10264–10284. https://doi.org/10.1080/21655979.2021.1990193
Jiang X, Sun J, Guo S, Zhao Z, Chen Y, Cao J, Liu Y, Cheng G, Tian L, Li Y (2023) Elsholtzia bodinieri Vaniot ameliorated acute lung injury in mice by regulating pyroptosis, inflammation, oxidative stress and macrophage polarization. J Ethnopharmacol. 307:116232. https://doi.org/10.1016/j.jep.2023.116232
Kalichman L, Hunter DJ (2007) Lumbar facet joint osteoarthritis: a review. Semin Arthritis Rheum 37:69–80. https://doi.org/10.1016/j.semarthrit.2007.01.007
Kang D (2016) Anti-adhesion effect of absorbable biomaterials in tendon injury reconstruction. Chin J Tissue Eng Res 20:3185–3192
Kim SU, Lee HJ, Kim YB (2013) Neural stem cell-based treatment for neurodegenerative diseases. Neuropathology 33:491–504. https://doi.org/10.1111/neup.12020
Knezevic NN, Candido KD, Vlaeyen JWS, Van Zundert J, Cohen SP (2021) Low back pain. Lancet 398:78–92. https://doi.org/10.1016/S0140-6736(21)00733-9
Laboute T, Zucca S, Holcomb M, Patil DN, Garza C, Wheatley BA, Roy RN, Forli S, Martemyanov KA (2023) Orphan receptor GPR158 serves as a metabotropic glycine receptor: mGlyR. Science (New York, NY) 379(6639):1352–1358. https://doi.org/10.1126/science.add7150
Lane CA, Hardy J, Schott JM (2018) Alzheimer’s disease. Eur J Neurol 25:59–70. https://doi.org/10.1111/ene.13439
Li S, He J (2018) Pilose antler polypeptide protects against sevoflurane-mediated neurocyte injury. Mol Med Rep 18:5353–5360. https://doi.org/10.3892/mmr.2018.9582
Li L, Yang F, Jia R, Yan P, Ma L (2020) Velvet antler polypeptide prevents the disruption of hepatic tight junctions via inhibiting oxidative stress in cholestatic mice and liver cell lines. Food Funct 11:9752–9763. https://doi.org/10.1039/d0fo01899f
Li M, Li Q, Dong H, Zhao S, Ning J, Bai X, Yue X, Xie A (2022) Pilose antler polypeptides enhance chemotherapy effects in triple-negative breast cancer by activating the adaptive immune system. Int J Biol Macromol 222:2628–2638. https://doi.org/10.1016/j.ijbiomac.2022.10.045
Li L, Yu Y, Wu W, Wang P (2023) Extraction, characterization and osteogenic activity of a type I collagen from starfish (Asterias amurensis). Mar Drugs 21(5):274. https://doi.org/10.3390/md21050274
Lin JH, Deng LX, Wu ZY, Chen L, Zhang L (2011) Pilose antler polypeptides promote chondrocyte proliferation via the tyrosine kinase signaling pathway. J Occup Med Toxicol 6:27. https://doi.org/10.1186/1745-6673-6-27
Liu G, Ma C, Wang P, Zhang P, Qu X, Liu S, Zhai Z, Yu D, Gao J, Liang J, Dai W, Zhou L, Xia M, Yang H (2017b) Pilose antler peptide potentiates osteoblast differentiation and inhibits osteoclastogenesis via manipulating the NF-κB pathway. Biochem Biophys Res Commun 491:388–395. https://doi.org/10.1016/j.bbrc.2017.07.091
Liu YY, Ding YF, Sui HJ, Liu W, Zhang ZQ, Li F (2023a) Pilose antler (Cervus elaphus Linnaeus) polysaccharide and polypeptide extract inhibits bone resorption in high turnover type osteoporosis by stimulating the MAKP and MMP-9 signaling pathways. J Ethnopharmacol 304:116052. https://doi.org/10.1016/j.jep.2022.116052
Liu H, Hu Y, Wu X, Hu R, Liu Y (2023b) Optimization of surface-engineered micropatterns on bacterial cellulose for guided scar-free skin wound healing. Biomolecules 13(5):793. https://doi.org/10.3390/biom13050793
Liu HT, Dong YM. Wang L, Zhou YN, Xing XM, Yang FH (2017a) Research progress on the taxonomy and phylogeny of deer animals in China. Chin J Wildlife 38: 514–523. https://doi.org/10.19711/j.cnki.issn2310-14902017a.03.029
Liu X, Yang Q, Li H, Lan X, Kan M, Lin J, Wang J, Zhang Z, Ming S, Li Z, Liu Y, Zhang Y, Pang Q, Gao S, Li N (2021) The anti-aging effect of velvet antler polypeptide is dependent on modulation of the gut microbiota and regulation of the PPARα/APOE4 pathway. Integr Neurosci 20: 573–583. https://doi.org/10.31083/j.jin2003061
Lu LJ, Chen L, Meng XT, Yang F, Zhang ZX, Chen D (2005) Biological effect of velvet antler polypeptides on neural stem cells from embryonic rat brain. Chin Med J (Engl) 118:38–42
Lu CW, Yeh KC, Chiu KM, Lee MY, Lin TY, Wang SJ (2022) The effect of isosaponarin derived from wasabi leaves on glutamate release in rat synaptosomes and its underlying mechanism. Int J Mol Sci 23(15):8752. https://doi.org/10.3390/ijms23158752
Luise D, Correa F, Stefanelli C, Simongiovanni A, Chalvon-Demersay T, Zini M, Fusco L, Bosi P, Trevisi P (2023) Productive and physiological implications of top-dress addition of branched-chain amino acids and arginine on lactating sows and offspring. J Anim Sci Biotechnol 14(1):40. https://doi.org/10.1186/s40104-022-00819-8
Ma C, Long H, Yang C, Cai W, Zhang T, Zhao W (2017) Anti-inflammatory role of pilose antler peptide in LPS-induced lung injury. Inflammation 40:904–912. https://doi.org/10.1007/s10753-017-0535-3
Ma S, Cong Z, Chen H, Wen H, Cao L, Liu C, Yang F, Liao Y (2021) Velvet antler polypeptide-loaded polyvinyl alcohol-sodium alginate hydrogels promote the differentiation of neural progenitor cells in 3D towards oligodendrocytes in vitro. Eur J Pharm Sci 167:106003. https://doi.org/10.1016/j.ejps.2021.106003
Murphy SL, Xu J, Kochanek KD, Arias E (2018) Mortality in the United States, 2017. NCHS Data Brief 328:1–8
Ni Y, Wang Z, Ma L, Yang L, Wu T, Fu Z (2019) Pilose antler polypeptides ameliorate inflammation and oxidative stress and improves gut microbiota in hypoxic-ischemic injured rats. Nutr Res 4:93–108. https://doi.org/10.1016/j.nutres.2019.01.005
Panikkar M, Attia E, Dardak S (2021) Osteoarthritis: a review of novel treatments and drug targets. Cureus 13:e20026. https://doi.org/10.7759/cureus.20026
Perolat R, Kastler A, Nicot B, Pellat JM, Tahon F, Attye A, Heck O, Boubagra K, Grand S, Krainik A (2018) Facet joint syndrome: from diagnosis to interventional management. Insights Imaging 9:773–789. https://doi.org/10.1007/s13244-018-0638-x
Qiang N, Lin W, Zhou X, Liu Z, Lu M, Qiu S, Tang S, Zhu J (2021) Electrospun fibers derived from peptide coupled amphiphilic copolymers for dorsal root ganglion (DRG) outgrowth. Gels (Basel, Switzerland) 7(4):196. https://doi.org/10.3390/gels7040196
Ray S, Adelnia H, Ta HT (2021) Collagen and the effect of poly-l-lactic acid based materials on its synthesis. Biomater Sci 9(17):5714–5731. https://doi.org/10.1039/d1bm00516b
Ren C, Gong W, Li F, Xie M (2019) Protective and therapeutic effects of Pilose antler against kidney deficiency-induced osteoporosis. Cell Mol Biol (Noisy-le-grand) 65:24–31
Rocha CV, Gonçalves V, da Silva MC, Bañobre-López M, Gallo J (2022) PLGA-based composites for various biomedical applications. Int J Mol Sci 23:2034. https://doi.org/10.3390/ijms23042034
Rodriguez D, Lavie CJ, Elagizi A, Milani RV (2022) Update on omega-3 polyunsaturated fatty acids on cardiovascular health. Nutrients 14:5146. https://doi.org/10.3390/nu14235146
Sharma L (2021) Osteoarthritis of the Knee. N Engl J Med 384:51–59. https://doi.org/10.1056/NEJMcp1903768
Shaw TD, McAuley DF, O’Kane CM (2019) Emerging drugs for treating the acute respiratory distress syndrome. Expert Opin, Emerg 24:29–41. https://doi.org/10.1080/14728214.2019.1591369
Su JL, Chiou J, Tang C, Zhao HM, Tsai CH, Chen PS, Chang YW, Chien MH, Peng C, Hsiao YM, Kuo ML, Yen ML (2010) CYR61 regulates BMP-2-dependent osteoblast differentiation through the {alpha}v{beta}3 integrin/integrin-linked kinase/ERK pathway. J Biol Chem 285(41):31325–31336. https://doi.org/10.1074/jbc.M109.087122
Sui Z, Zhang L, HuoY ZY (2014) Bioactive components of velvet antlers and their pharmacological properties. J Pharm Biomed Anal 87:229–240. https://doi.org/10.1016/j.jpba.2013.07.044
Ter Hark SE, Vos CF, Aarnoutse RE, Schene AH, Coenen MJH, Janzing JGE (2022) Biomarkers as predictors of treatment response to tricyclic antidepressants in major depressive disorder: a systematic review. J Psychiatr Res 150:202–213. https://doi.org/10.1016/j.jpsychires.2022.03.057
Vitaloni M, Botto-van Bemden A, Sciortino Contreras RM, Scotton D, Bibas M, Quintero M, Monfort J, Carné X, de Abajo F, Oswald E, Cabot MR, Matucci M, du Souich P, Möller I, Eakin G, Verges J (2019) Global management of patients with knee osteoarthritis begins with quality of life assessment: a systematic review. BMC Musculoskelet Disord 20:493. https://doi.org/10.1186/s12891-019-2895-3
Vogel A, Meyer T, Sapisochin G, Salem R, Saborowski A (2022) Hepatocellular carcinoma. Lancet 400:1345–1362. https://doi.org/10.1016/S0140-6736(22)01200-4
Wang J, Sun X, Zhang Z, Wang Y, Huang C, Yang C, Liu L, Zhang Q (2019a) Silk fibroin/collagen/hyaluronic acid scaffold incorporating pilose antler polypeptides microspheres for cartilage tissue engineering. Mater Sci Eng C Mater Biol Appl 94:35–44. https://doi.org/10.1016/j.msec.2018.09.017
Wang W, Zhang J, Yang X, Huang F (2019b) Hypoglycemic activity of CPU2206: A novel peptide from sika (Cervus nippon Temminck) antler. J Food Biochem 43:e13063. https://doi.org/10.1111/jfbc.13063
Wang X, Li H, Liu Y, Wu H, Wang H, Jin S, Lu Y, Chang S, Liu R, Peng Y, Guo Z, Wang X (2020a) Velvet antler methanol extracts (MEs) protects against oxidative stress in Caenorhabditis elegans by SKN-1. Biomed Pharmacother 121:109668. https://doi.org/10.1016/j.biopha.2019.109668
Wang P, Sun TF, Li G, Zhang HM, Liu FJ, Gao ZH, Cao SN, Sun GD, Du HT, Wang CA, Wang DD, Shi B, Lin L (2020b) The separation of antler polypeptide and its effects on the proliferation and osteogenetic differentiation of bone marrow mesenchymal stem cells. Evid Based Complement Alternat Med 2020:1294151. https://doi.org/10.1155/2020/1294151
Weng L, Zhou Ql, Chi DQ, Wang BX (2001) A new polypeptide promoting epidermal cells and chondrocytes proliferation from Cervus elaphus Linnaeus. Acta Pharmaceutica Sinica 12: 913–916. https://doi.org/10.16438/j.0513-4870.2001.12.009.
Wu J, Tian Y, Han L, Liu C, Sun T, Li L, Yu Y, Lamichhane B, D’Souza RN, Millar SE, Krumlauf R, Ornitz DM, Feng JQ, Klein O, Zhao H, Zhang F, Linhardt RJ, Wang X (2020) FAM20B-catalyzed glycosaminoglycans control murine tooth number by restricting FGFR2b signaling. BMC Biol 18(1):87. https://doi.org/10.1186/s12915-020-00813-4
Xia P, Liu D, Jiao Y, Wang Z, Chen X, Zheng S, Fang J, Hao L (2022) Health Effects of Peptides Extracted from Deer Antler. Nutrients 14:4183. https://doi.org/10.3390/nu14194183
Xie WQ, Zhao YJ, Li F, Shu B, Lin SR, Sun L, Wang YJ, Zheng HX (2019) Velvet antler polypeptide partially rescue facet joint osteoarthritis-like phenotype in adult β-catenin conditional activation mice. BMC Complement Altern Med 19:191. https://doi.org/10.1186/s12906-019-2607-4
Xin JL, Zhang Y, Li Y, Zhang LZ, Lin Y, Zheng LW (2017) Protective effects of Cervus nippon Temminck velvet antler polypeptides against MPP+-induced cytotoxicity in SH-SY5Y neuroblastoma cells. Mol Med Rep 16:5143–5150. https://doi.org/10.3892/mmr.2017.7303
Xiu ZB, Lin JH, Wu CY, Wang RX (2011) Deer antler polypeptide induces in vitro differentiation of bone marrow mesenchymal stem cells to cartilage phenotype. Chin J Tissue Eng Res 15:3563–3566
Xu XY, Lu LJ, Kl W, Li Z, Chen XS, Jing XB (2007) Repair and reconstruction of tendon tissue by PLGA fiber carrying deer antler polypeptide. Chin J Rehabil Med 09:796–798
Xu L, Yan L, Tao W (2018) Pilose antler peptide attenuates high-fat-diet-induced liver injury. Toxicol Mech Methods 28:279–285. https://doi.org/10.1080/15376516.2017.1402978
Xu Y, Qu X, Zhou J, Lv G, Han D, Liu J, Liu Y, Chen Y, Qu P, Huang X (2021) Pilose antler peptide-3.2KD ameliorates adriamycin-induced myocardial injury through TGF-β/SMAD signaling pathway. Front Cardiovasc Med 8:659643. https://doi.org/10.3389/fcvm.2021.659643
Xu Z, Xie W, Feng Y, Wang Y, Li X, Liu J, Xiong Y, He Y, Chen L, Liu G, Wu Q (2022) Positive interaction between GPER and β-alanine in the dorsal root ganglion uncovers potential mechanisms: mediating continuous neuronal sensitization and neuroinflammation responses in neuropathic pain. J Neuroinflammation 19(1):164. https://doi.org/10.1186/s12974-022-02524-9
Xu Y, Zhou J, Lv GF, Liu YX, Zhao XT, Li X, Ye DD, Qu XB, Huang XW (2020) Effect of pilose antler peptide on doxorubicin-induced H9c2 cells injury via TGF-β/Smad/ERK signaling pathway. Pakistan J.Zool 52: 1787–1793. https://doi.org/10.17582/journal.pjz/20200218020203
Yan Y, Jiangwen C, Binbin L (2023) Mechanism and application of glycosaminoglycans in bone tissue engineering. China Tissue Eng Res 27(34):5538–5545
Yang Z, Yu H, Rao X, Liu Y, Pi M (2008) Effects of electroacupuncture at the conception vessel on proliferation and differentiation of nerve stem cells in the inferior zone of the lateral ventricle in cerebral ischemia rats. J Tradit Chin Med 28:58–63. https://doi.org/10.1016/s0254-6272(08)60015-1
Yang Q, Lin JN, Sui X, Li H, Kan M, Wang JF, Li J, Zhang Z, Liu XR, Ming ST, Qu XB, Li N, (2020) Antiapoptotic effects of velvet antler polypeptides on damaged neurons through the hypothalamic-pituitary-adrenal axis. J Integr Neurosci 19: 469–477. https://doi.org/10.31083/j.jin.2020.03.167
Yao SY, Wang JF, Xu Z, Meng Y, Xue Y, Yang F, Yao WB, Gao XD, Chen S (2023) A peptide rich in glycine-serine-alanine repeats ameliorates Alzheimer-type neurodegeneration. Br J Pharmacol 180(14):1878–1896. https://doi.org/10.1111/bph.16048
Yun C, Qian W, Wu J, Yuan C, Jiang S, Lv J (2020) Pilose antler peptide promotes osteoblast proliferation, differentiation and mineralization via the insulin signaling pathway. Exp Ther Med 19:923–930. https://doi.org/10.3892/etm.2019.8286
Zang ZJ, Tang HF, Tuo Y, Xing WJ, Ji SY, Gao Y, Deng CH (2016) Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice. Asian J Androl 18:613–619. https://doi.org/10.4103/1008-682X.166435
Zha E, Gao S, Pi Y, Li X, Wang Y, Yue X (2012) Wound healing by a 3.2 kDa recombinant polypeptide from velvet antler of Cervus nippon Temminck. Biotechnol Lett 34:789–793. https://doi.org/10.1007/s10529-011-0829-8
Zha E, Dandan L, Bai X, Zhou T, Li Y, Shenyang G, Yue X (2016) A recombinant polypeptide from velvet antler of Cervus nippon Temminck exhibits similar immunomodulatory effects as its natural counterpart. Int Immunopharmacol 38:385–389. https://doi.org/10.1080/08923973.2016.1233978
Zhang ZQ, Zhang Y, Wang BX, Zhou HO, Wang Y, Zhang H (1992) Purification and partial characterization of anti-inflammatory peptide from pilose antler of Cervus nippon Temminck. Yao Xue Xue Bao 27:321–324
Zhang Z, Liu X, Duan L, Li X, Zhang Y, Zhou Q (2011) The effects of velvet antler polypeptides on the phenotype and related biological indicators of osteoarthritic rabbit chondrocytes. Acta Biochim Pol 58:297–302
Zhang LZ, Xin JL, Zhang XP, Fu Q, Zhang Y, Zhou QL (2013) The anti-osteoporotic effect of velvet antler polypeptides from Cervus elaphus Linnaeus in ovariectomized rats. J Ethnopharmacol 150:181–186. https://doi.org/10.1016/j.jep.2013.08.029
Zhang M, Li N, Qu XB, Luo S, Drummen Gregor PC (2016) Total velvet-antler polypeptide extract from Cervus nippon Temminck induces cell proliferation and activation of the PI3K–Akt signalling pathway in human peripheral blood lymphocytes. Animal Production Science 56:1008–1015
Zhang L, Zhuang Z, Sun Y, Ma S, Yang W, Lei H, Ouyang J, Wang Y, Zuo J (2017) Velvet antler polypeptide is able to induce differentiation of neural stem cells towards neurons in vitro. J Tradit Chin Med 37:308–313
Zhang G, Wang D, Ren J, Sun H, Li J, Wang S, Shi L, Wang Z, Yao M, Zhao H, Li C (2022) Velvet antler peptides reduce scarring via inhibiting the TGF-β signaling pathway during wound healing. Front Med (Lausanne) 8:799789. https://doi.org/10.3389/fmed.2021.799789
Zhao L, Mi Y, Guan H, Xu Y, Mei Y (2016a) Velvet antler peptide prevents pressure overload-induced cardiac fibrosis via transforming growth factor (TGF)-β1 pathway inhibition. Eur J Pharmacol 783:33–46. https://doi.org/10.1016/j.ejphar.2016.04.039
Zhao L, Wang X, Zhang XL, Xie QF (2016b) Purification and identification of anti-inflammatory peptides derived from simulated gastrointestinal digests of velvet antler protein (Cervus elaphus Linnaeus). J Food Drug Anal 24:376–384. https://doi.org/10.1016/j.jfda.2015.10.003
Zhao S, Zuo W, Chen H, Bao T, Liu X, Sun T, Wang S (2019) Effects of pilose antler peptide on bleomycin-induced pulmonary fibrosis in mice. Biomed Pharmacother 109:2078–2083. https://doi.org/10.1016/j.biopha.2018.08.114
Zheng K, Li Q, Lin D, Zong X, Luo X, Yang M, Yue X, Ma S (2020) Peptidomic analysis of pilose antler and its inhibitory effect on triple-negative breast cancer at multiple sites. Food Funct 11:7481–7494. https://doi.org/10.1039/d0fo01531h11
Zhou QL, Guo YJ, Wang LJ, Wang Y, Liu YQ, Wang Y, Wang BX (1999) Velvet antler polypeptides promoted proliferation of chondrocytes and osteoblast precursors and fracture healing. Zhongguo Yao Li Xue Bao 20:279–282
Zhou QL, Liu YQ, Wang Y, Guo YJ, Wang BX (2001) A comparison of chemical composition and bioactivity of polypeptides from velvet antlers of Cervus nippon Temminck and Cervus elaphus Linnaeus. Acta Pharm Sin 26:699–702
Zhu W, Wang H, Zhang W, Xu N, Xu J, Li Y, Liu W, Lv S (2017) Protective effects and plausible mechanisms of antler-velvet polypeptide against hydrogen peroxide induced injury in human umbilical vein endothelial cells. Can J Physiol Pharmacol 95:610–619. https://doi.org/10.1139/cjpp-2016-0196
Funding
This work was supported by the Department of Science and Technology, Jilin Province, China (grant number YDZJ202201ZYTS249).
Author information
Authors and Affiliations
Contributions
He Sun: overall instructor; Dandan Xiao, Wei Liu, and Xue Li: resources and data collection; Zhe Lin and Yong Li: some constructive suggestions put forward for revising the article. Yuling Ding: final correction, editing, and approval. All authors have read and approved this paper for publication. The authors confirm that no paper mill and artificial intelligence was used.
Corresponding authors
Ethics declarations
Ethics approval
Not applicable.
Consent to participate
Not applicable.
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Additional information
Publisher's note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Supplementary Figure 1
(PNG 771 kb)
Supplementary Figure 2
(PNG 711 kb)
Supplementary Figure 3
(PNG 641 kb)
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Sun, H., Xiao, D., Liu, W. et al. Well-known polypeptides of deer antler velvet with key actives: modern pharmacological advances. Naunyn-Schmiedeberg's Arch Pharmacol 397, 15–31 (2024). https://doi.org/10.1007/s00210-023-02642-y
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00210-023-02642-y