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      Latest ReseachAngiogenesis - that is the growth of blood vessels has been recently intensively researched in New Zealand. Deer velvet grows at up to 2cm per day. This means that all support tissues, including blood vessels must also grow at that rate. The question is how can they do this? Is it possible that deer velvet possesses unique factors which can allow blood vessels to grow that fast. One way of showing that a substance causes blood vessel 
          growth is to test it on fertilised chickens's eggs. As the chicken embryo 
          develops in the egg, blood vessels grow out and surround the egg white. 
          It is possible to treat small areas with test substances; those that 
          reduce blood vessel growth will leave a space, those that stimulate 
          blood vessel growth will cause an increase in the density of blood vessels. 
          Extracts from deer velvet have been shown to increase the number of 
          blood vessels. A second way of showing that deer velvet causes blood 
          vessels to grow is to take small pieces of adult deer arteries and put 
          them in tissue culture. You can then add test substances and see if 
          they cause outgrowths. Deer velvet extracts clearly showed filamentous 
          threads of new blood vessels growing out from the artery. This means 
          that the deer velvet extract causes new blood vessels to grow. Taking these results together it is clear that there are 
          factors in deer velvet which promote blood vessel growth. There are 
          likely to be therapeutic properties, for example in tissue repair and 
          wound healing. Deer velvet is unique in that it is the only mammalian 
          organ to fully regenerate each year. It follows that there are likely 
          to be unique factors which are responsible for this property.  It can be concluded that there are novel factors in deer 
          velvet, which are not present elsewhere in the body. These factors could 
          be markers for deer velvet in dietary supplements or be novel action 
          ingredients for new supplements. Exploring the mechanisms regulating regeneration of deer antlers. Price,-J; Allen,-S London, UK: Royal Society.  The effects of elk velvet antler consumption on the 
          rat: development, behavior, toxicity and the activity of liver gamma Hemmings,-S-J; Song-XiuYuan Moreau,-M; Dupuis,-J; Bonneau,-N-H; Lecuyer,-M Canadian-Veterinary-Journal. 2004; 45(2): 133-139. A powder of quality elk velvet antler (QEVA) was evaluated 
          on client-owned dogs with osteoarthrosis (OA) in a clinical, double-blind, 
          and placebo-controlled study. Thirteen dogs received a placebo for 30 
          days and then QEVA for 60 days. Twenty-five other dogs received QEVA 
          for 60 days. Gait analysis measured with a force plate, clinical signs 
          assessed by an orthopedic surgeon, performances in daily life activities 
          and vitality assessed by the owners, and complete blood analyses were 
          obtained at days 0, after 30 days of placebo and/or 60 days of QEVA. 
          On placebo, the 13 dogs did not show significant improvement (P<0.05); 
          however, their gait, their performances in daily life activities, and 
          their vitality were significantly improved on QEVA, based on changes 
          in values exceeding those observed when placebo was administered. The 
          25 dogs on QEVA for 60 days showed similar improvements. No clinical 
          changes were revealed on blood analyses. Administration of QEVA was 
          effective in alleviating the condition in arthritic dogs. Effect of deer antler drink supplementation on blood 
          pressure blood glucose and lymphocyte DNA damage in type 2 diabetic 
          patients. Kim-HyeYoung; Jeon-EunJae; Park-YooKyoung; Kang-MyungHee Korean-Journal-of-Nutrition. 2004; 37(9): 794-800. Barling,-P-M; Liu-Hong; Matich,-J; Mount,-J; Lai-KaWai-[Lai,-K-W-A]; 
          Ma-Li; Nicholson,-L-F-B Cell-Biology-International. 2004; 28(10): 661-673. Bao-HaiYing Journal-of-Economic-Animal. 2004; 8(2): 74-77. Kim-KiHwan; Lee-EuiJung; Kim-Kilhyoun; Han-SoYeop; Jhon-GilJa Nutrition-. 2004; 20(4): 394-401. OBJECTIVE: The immunomodulatory effect of deer antler, which is used as traditional medicine, has been known, but the active component of antlers from Cervus elaphus has not been identified. In this study, we identified the immunomodulator from C. elaphus and examined its biological activities on the immune system. METHODS: To identify an immunomodulator, we used bioassay-guided 
          fractionation after silica gel column chromatography. Structural analysis 
          was performed with one- and two-dimensional nuclear magnetic resonance 
          techniques and tandem mass The effects of deer antler velvet extract or powder supplementation on aerobic power, erythropoiesis, and muscular strength and endurance characteristics. Sleivert G, Burke V, Palmer C, Walmsley A, Gerrard D, Haines S, Littlejohn R. Faculty of Kinesiology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 5A3. Int J Sport Nutr Exerc Metab. 2003 Sep;13(3):251-65. To determine the effects of deer antler velvet on maximal aerobic performance and the trainability of muscular strength and endurance, 38 active males were randomly assigned in a double-blind fashion to either deer antler velvet extract (n = 12), powder (n = 13), or placebo groups (n = 13). Subjects were tested prior to beginning supplementation and a 10-week strength program, and immediately post-training. All subjects were measured for circulating levels of testosterone, insulin-like growth factor, erythropoietin, red cell mass, plasma volume, and total blood volume. Additionally, muscular strength, endurance, and VO2max were determined. All groups improved 6 RM strength equivalently (41 +/- 26%, p < .001), but there was a greater increase in isokinetic knee extensor strength (30 +/- 21% vs. 13 +/- 15%, p = .04) and endurance (21 +/- 19% vs. 7 +/- 12%, p = .02) in the powder compared to placebo group. There were no endocrine, red cell mass or VO2max changes in any group. These findings do not support an erythropoetic or aerobic ergogenic effect of deer antler velvet. Further, the inconsistent findings regarding the effects of deer antler velvet powder supplementation on the development of strength suggests that further work is required to test the robustness of the observation that this supplement enhances the strength training response and to ensure this observation is not a type I error. Elk velvet antler in rheumatoid arthritis: phase II trial. Allen M, Oberle K, Grace M, Russell A. Faculty of Nursing, University of Alberta, Edmonton, Canada. marion.allen@ualberta.ca Biol Res Nurs. 2002 Jan;3(3):111-8. The purpose of this phase II clinical trial was to examine safety of elk velvet antler taken concurrently with rheumatoid arthritis medications and to determine efficacy by dose to enable sample size estimation and dose standardization for a larger study. Forty patients with stage II rheumatoid arthritis were randomly assigned to 1 of 4 arms of 10 patients each. One group received placebo and the other 3 groups received 2, 4, or 6 capsules (215 mg) of elk velvet antler with appropriate placebos to total 6 capsules daily. All subjects continued to take their arthritis medications. Outcome variables were reported adverse events and health status. At 1 month, there were no significant differences between groups in number of adverse events or health status. The greatest improvement was in the 6 elk velvet antler group, the least was in the placebo group. Differences were not statistically significant. It was concluded that elk velvet antler can be taken safely in conjunction with a number of rheumatoid arthritis medications and should be studied further to assess efficacy. Velvet antler polypeptides promoted proliferation of chondrocytes and osteoblast precursors and fracture healing. Zhou QL, Guo YJ, Wang LJ, Wang Y, Liu YQ, Wang Y, Wang BX. Research Centre of New Drug, Changchun College of Traditional Chinese Medicine, China. AIM: To study the effects of velvet antler (VA) total 
          polypeptides (VATP) and VA polypeptides, VAP-A, VAP-B, and VAP-C on 
          proliferation of chondrocytes and osteoblast precusors. METHODS: Chondrocytes 
          (rabbit and human fetus) and osteoblast precusors (chick embryo) were 
          incubated in the culture medium containing VATP or VAP-A, VAP-B, and 
          VAP-C. [3H]TdR incorporation into DNA was measured. Fracture healing-promoting 
          action of VATP was determined in rats. RESULTS: VATP 50-200 mg.L-1 and 
          VAP-B 12.5, 25, and 50 mg.L-1 showed most marked proliferation-promoting 
          activity for rabbit costed chondrocytes and increased incorporation 
          of [3H]TdR from (73 +/- 9) Bq (control group) to (272 +/- 55), (327 
          +/- 38), and (415 +/- 32) Bq, respectively (P < 0.01). The activity 
          of VAP-A was weaker than that of VAP-B, and VAP-C had no activity. VATP 
          10 and 20 mg.kg-1 by local injection into the cross-section fracture 
          area accelerated healing of radial fracture. The healing rate of VATP-treated 
          group was higher (75%) than that of control group (25%) (P < 0.05). 
          CONCLUSION: VATP accelerated fracture healing by stimulating proliferation 
          of chondrocytes and osteoblast precursors. Comparative analysis of contents of amino acid, total 
          phospholipid, calcium and phosphorus in sika deer velvet bone slices 
          with blood and without blood.  Wang-YanMei; Chu-LiWei; Wang-YanHong; Wang-ShuLi; Wang-YM; 
          Chu-LW; Wang-YH; Wang-SL  Journal-of-Economic-Animal. 2003, 7: 2, 21-23; 8 ref. Influence of powdered velvet antler on growth and intestinal 
          organ development in Sprague-Dawley Rats. Sung-HG; Kim-DK; Shin-HT Journal-of-Animal-Science-and-Technology. 2003, 45: 5, 
          749-758; 33 ref. Modification of concanavalin A-dependent proliferation by phosphatidylcholines isolated from deer antler, Cervus elaphus.  Kim-KiHwan; Lee-EuiJung; Kim-Kilhyoun; 
          Han-SoYeop; Jhon-GilJa; Kim-KH; Lee Nutrition. 2004, 20: 4, 394-401; 29 ref. CONCLUSIONS: These data collectively 
          suggest that phosphatidylcholines with saturated fatty acyl chains are 
          immunostimulating factors. They may modify the proliferation of known 
          mitogens. Further, chain length and saturation of the fatty acids may 
          play important roles in the proliferation of spleen cells. Cells in regenerating deer antler cartilage provide 
          a microenvironment that supports osteoclast differentiation. Faucheux-C; Nesbitt-SA; Horton-MA; Price-JS Journal-of-Experimental-Biology. 2001, 204: 3, 443-455; 
          Many ref. Lysophosphatidylcholine derived from deer antler extract suppresses hyphal transition in Candida albicans through MAP kinase pathway. Min-Juyoung; Lee-YounJin; Kim-YoungAh; Park-HyunSook; 
          Han-SoYeop; Jhon -GilJa; Choi-Wonja; Min-J; Lee-YJ; Kim-YA; Park-HS; 
          Han-SY; Jhon-GJ; Choi-W Biochimica-et-Biophysica-Acta,-Molecular-and-Cell-Biology-of-Lipids. 
          2001, 1531: 1-2, 77-89; 35 ref.  A study on the intake patterns of health food of the 
          elderly aged over 60 years in the Chuncheon area.  Rhee-HeeSeoup; Lee-HaiSook; Yee-JungAe; Kang-KeumJee; 
          Rhee-HS; Lee-HS; Yee-JA; Kang-KJ Deer antler : scientific review. Les bois de cerf : revue de litterature scientifique. Crigel-MH; Balligand-M; Heinen-E Annales-de-Medecine-Veterinaire. 2001, 145: 1, 25-38; 
          100 ref. Toxicological evaluation of New Zealand deer velvet powder. Part I: acute and subchronic oral toxicity studies in rats.Zhang-H; Wanwimolruk-S; Coville-PF; Schofield-JC; Williams-G; 
          Haines-SR; Food-and-Chemical-Toxicology. 2000, 38: 11, 985-990; 13 ref.  Potential toxic effects of acute and subchronic dosage 
          regimens of deer velvet powder have been assessed in rats following 
          OECD guidelines. In the acute study, rats of both sexes were exposed 
          to a single dose of 2 g/kg body weight. There was no mortality or other 
          signs of toxicity during 14 days' observation. Furthermore, no significant 
          alteration either in relative organ weights or their histology was discernible 
          at terminal autopsy. In the 90-day subchronic study, deer velvet was 
          administered in 1 g/kg daily doses by gavage to rats. A control group 
          of rats received water only. There was no effect on body weight, food 
          consumption, clinical However, there was a significant difference (P < 0.05) in the group meanrelative liver weight (3.52±0.30 vs 3.81±0.26 g/100 g body weight) of deer velvet-treated and control male rats. The gross necropsy and pathological examination of rats treated with deer velvet did not reveal any abnormalities in tissue morphology. Based on these results, it may be concluded that rats had no deer velvet treatment-related toxicological and histopathological abnormalities at the doses administered, despite the observed minor changes in liver weight. Cells in regenerating deer antler cartilage provide 
          a microenvironment that Faucheux-C; Nesbitt-SA; Horton-MA; Price-JS Journal-of-Experimental-Biology. 2001, 204: 3, 443-455; Many ref. Lysophosphatidylcholine derived from deer antler extract 
          suppresses hyphal Min-Juyoung; Lee-YounJin; Kim-YoungAh; Park-HyunSook; 
          Han-SoYeop; Jhon Biochimica-et-Biophysica-Acta,-Molecular-and-Cell-Biology-of-Lipids. 
          2001, A family of 2-lysophosphatidylcholines (lyso-PCs) was 
          isolated from deerantler extract, guided exclusively by hyphal transition 
          inhibitory activity in Candida albicans. Structural determination of 
          the isolated lyso-PCs by spectroscopic methods, including infrared spectroscopy, 
          1H nuclear magnetic resonance (NMR), 13C NMR, 2D correlation spectroscopy 
          NMR, fast atom bombardment mass spectrometry and tandem mass spectrometry, 
          confirmed that the natural products were composed of at least 4 different The major lyso-PCs were confirmed as 1-stearoyl-, 1-oleoyl-, 
          1-linoleoyl- and 1-palmitoyl-2-lyso-sn-glycero-3-phosphatidylcholines. 
          Lyso-PC specifically suppressed the morphogenic transition from yeast 
          to hyphae in C. albicans, without affecting the growth of either yeast 
          or hyphae. Lyso-PC exerted hyphal transition that suppressed activity 
          in the broad spectrum of the Candida species, such as C. albicans, C. 
          krusei, C. guilliermondii and C. parapsilosis. Northern analysis indicated 
          that the Concentrations of insulin-like growth factor-I in adult 
          male white-tailed Ditchkoff-SS; Spicer-LJ; Masters-RE; Lochmiller-RL Comparative-Biochemistry-and-Physiology.-A,-Molecular-and-Integrative Our understanding of insulin-like growth factor-I (IGF-I) 
          in cervids has been limited mostly to its effects on antler development 
          in red deer (Cervus elaphus), roe deer (Capreolus capreolus), fallow 
          deer (Dama dama),and pudu (Pudu puda). Although IGF-I has been found 
          to play a critical role in reproductive function of other mammals, its 
          role in reproduction of deer is unknown. The objectives of the present 
          study were to determine if serum levels of IGF-I change during the breeding 
          season, assess whether age influences serum IGF-I, compare levels of 
          IGF-I measured during and following the breeding season, and determine 
          if IGF-I is associated with Potential uses of velvet antler as nutraceuticals, 
          functional and medical Sunwoo-HH; Sim-JS Journal-of-Nutraceuticals,-Functional-and-Medical-Foods. 
          2000, 2: 3, 5-23; Velvet antlers have been used as Oriental medicine for many centuries.Traditional medical reports and clinical observations from the Eastern world convincingly show that velvet antler is biologically active.However, little information is available on chemical and biological efficacy of antler products in the West due to the incomplete understanding of the uses and pharmacological properties of velvet antlers. To make antler products acceptable as nutraceuticals and functional foods in the West, antler research has been conducted to isolate and characterize the chemical and biological properties of velvet antlers. The chemical composition of antler was determined in four sections (tip, upper, middle, and base). Contents of dry matter, collagen, ash, calcium, phosphorus, and magnesium increased (P<0.05), and those of protein and lipid decreased (P<0.05) downward from the tip to the base. The concentrations of uronic acid, sulfated glycosaminoglycan 
          (GAG), and sialic acid decreased (P<0.05) downward. Amino acid and 
          fatty acid contents, expressed as percentage of total protein and lipid, 
          respectively, also varied (P<0.05) among sections. The yield of chondroitin 
          sulfate (CS) was approximately six fold greater in the cartilaginous 
          (tip and upper) sections than in the bony (middle and base) sections. 
          In addition to CS, the antler sections contained small amounts of keratan 
          sulfate (KS), hyaluronic acid, and dermatan sulfate. Two proteoglycans 
          associated with GAGs were also extracted from the cartilaginous section; 
          a large aggregated proteoglycan with CS and KS and small molecules of 
          decorin. Water soluble extracts rich in GAG stimulated Effects of insulin-like growth factor 1 and testosterone 
          on the Li-ChunYi; Littlejohn-RP; Suttie-JM; Li-CY Journal-of-Experimental-Zoology. 1999, 284: 1, 82-90; 27 ref. The aim of this study was to use cell culture techniques 
          to investigate how testosterone and IGF1 affects the proliferation of 
          antlerogenic cells from the four ossification stages of pedicle/antler 
          in vitro. The results showed that in serum-free medium IGF1 stimulated 
          the proliferation of antlerogenic cells from all four ossification stages 
          (intramembraneous (IMO), transistional (OPC), pedicle endrochondral 
          (pECO) and antler enfochondral (aECO)) in a dose-dependent manner. In 
          contrast, testosterone However, in the presence of IGF1, testosterone increased 
          proliferation of the antlerogenic cells from the IMO and the OPC stages 
          (pedicle tissue), and reduced proliferation of the antlerogenic cells 
          from transformation point (TP) and aECO stages (antler tissue). Therefore, 
          the results from the present in vitro study support the in vivo findings 
          that androgen hormones stimulate pedicle formation but inhibit antler 
          growth. The change in the mitogenic effects of testosterone on antlerogenic 
          cells from positive to negative occurs approximately at the change in 
          ossification type from OPC to pECO. Therefore, these results reinforce 
          the hypothesis 
 Kameyama-Y; Takahashi-R; Ito-M; Maru-R; Ishijima-Y Animal-Science-Journal. 2000, 71: 2, 137-142; 23 ref. Annual changes in the concentration of serum testosterone (T) in sika deer stags were examined. The relationships between T concentration and the size of testis, and between T concentration and the antler cycle were also evaluated. T concentration increased between July and September, then decreased between October and November. The highest T concentration was noted in September or October. During the period from November to the following July, T concentration remained low. The volume of the testis and scrotal circumference showed changes similar to those in the T concentration. The testis volume showed clearer seasonal changes than those of the scrotal circumference. Shedding of velvets was observed during the period of high T concentrations. It is concluded that there are distinct annual changes in the blood T concentration in sika deer stags, which are related to the annual changes in testis volumes, scrotal circumferences and antlers. Antinarcotic effects of the velvet antler water extract on morphine in mice. Kim-HackSeang; Lim-HwaKyung; Park-WooKyu; Kim-HS; Lim-HK; Park-WK Journal-of-Ethnopharmacology. 1999, 66: 1, 41-49; 35 ref. The present study was undertaken to investigate the antinarcotic 
          effects of velvet antler water extract (VAWE) from Cervus elaphus on 
          morphine in mice. Morphine-induced analgesic action was measured by 
          the tail-flick method. Morphine-induced hyperactivity and reverse tolerance 
          were evidenced by measuring the enhanced ambulatory activity using a 
          tilting -type ambulometer. Dopamine (DA) receptor supersensitivity in 
          mice displaying morphine-induced reverse tolerance was evidenced by 
          the Effect of water-soluble extract from antler of wapiti 
          (Cervus elaphus) on Sunwoo-HH; Nakano-T; Sim-JS Canadian-Journal-of-Animal-Science. 1997, 77: 2, 343-345; 7 ref. Water-soluble extracts were prepared from the tip sections of antlers of 4 -year-old wapiti stags, and the effect of the extract on the growth of bovine skin fibroblasts in culture was examined. The results showed the presence of growth promoting factor(s) in the antler extract. The stimulation of cell growth was found to be dose-dependent (P<0.05). Glycosaminoglycans from growing antlers of wapiti (Cervus 
          elaphus). Canadian-Journal-of-Animal-Science. 1997, 77: 4, 715-721; 33 ref. The emerging wapiti industry in North America is based 
          largely on markets for velvet antlers which are used in oriental medicine. 
          Despite the economic opportunity, enthusiasm has been dampened by incomplete 
          understanding of the chemical and pharmacological properties of velvet 
          antler. This study characterizes polysaccharide constituents of glycosaminoglycans 
          in growing antler of wapiti (Cervus elaphus). Glycosaminoglycans were 
          isolated from four sections (tip, upper, middle and base) of growing 
          antlers, and were studied using cellulose acetate electrophoresis, gel 
          electrophoresis, enzymic digestion and gel chromatography. The tip and 
          upper sections of the antler which are rich in cartilaginous tissues 
          contained chondroitin sulfate as a major glycosaminoglycan with small 
          amounts of hyaluronic acid. In the middle and base sections containing 
          bone and bone marrow, chondroitin sulfate was 
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