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Effects of Rhodiola on production, health and gut development of broilers reared at high altitude in Tibet

Scientific Reports volume 4, Article number: 7166 (2014) | Download Citation


Rhodiola has long been used as a traditional medicine to increase resistance to physical stress in humans in Tibet. The current study was designed to investigate whether Rhodiola crenulata (R. crenulata) could alleviate the negative effects of hypoxia on broiler chickens reared in Tibet Plateau. The effect of supplementing crushed roots of R. crenulata on production performance, health and intestinal morphology in commercial male broilers was investigated. Dietary treatments included CTL (basal diet), Low-R (basal diet + 0.5% R. crenulata) and High-R (basal diet + 1.5% R. crenulata). In comparison with broilers fed the control diet, Low-R had no effect on production performance while High-R significantly decreased average daily feed intake at d14, 28 and 42, body weight at d28 and 42 and gut development. Ascites induced mortality did not differ among treatments. Nevertheless Low-R significantly reduced non-ascites induced mortality and total mortality compared with broilers fed CTL and High-R diets. Broilers fed the High-R diet had significantly increased blood red blood cell counts and hemoglobin levels at 28d compared with other treatments. Our results suggest that supplementation with Rhodiola might reduce the effects of hypoxia on broilers and consequently decrease mortality rate.


Poultry production in Tibet, China is increasing rapidly. It is well known that indigenous Tibet chickens are well adapted to high altitude environments and they mainly inhabit the areas around the midstream of Brahmaputra and Sanjiang rivers (about 2200 to 4000 m above sea level)1. Nevertheless, it has been a common practice for most poultry farmers in Tibet to raise commercial broiler chickens taking advantage of their fast growth rates acquired following intensive selection for this trait. However, these chickens are not well adapted to hypoxia, a main ecological factor with a negative impact on animal welfare and a threat to the survival of organisms in high altitude areas. Hypoxia refers to a low partial pressure of O2 in the inspired air. The partial pressure of O2 decreases with increasing altitude. Reduced levels of inspired O2 triggered acute pulmonary vasoconstriction and pulmonary hypertension in broilers2. Broilers raised in hypoxic environments exhibited lower growth performance3,4, altered gut development5 and blood parameters6, increased pulmonary arterial pressure and right ventricular hypertrophy7,8, and more importantly, increased mortality rates, especially ascites induced mortality3,4. Cost-effective measures are needed to ameliorate hypoxia induced negative effects on broiler production in Tibet and other high altitude regions.

Ascites is a cardiovascular metabolic disorder characterized by fluid accumulation in the abdominal cavity4. An estimated 4.7% of broilers worldwide have ascites, which causes great economic losses to the broiler industry9. The high incidence of ascites syndrome in modern broiler lines can be attributed to three major reasons as summarized by Kalmar et al10. Firstly, a superior growth rate inherently implies a high oxygen demand to sustain metabolic needs; secondly, the increased growth rate of modern broilers results in a significant reduction in relative heart and lung size, and thus diminished cardiopulmonary capacity; and thirdly, an increase in metabolic rates not only augments oxygen requirement at the tissue level, but also elevates mitochondrial production of reactive oxygen species10. The rate of ascites incidence could be much higher when commercial broiler strains are reared at high altitudes. Much effort has been made to prevent ascites syndrome in boiler chickens. Genetic selection for ascites resistant broiler lines could be a permanent solution. However, no such broiler lines have been successfully developed. Thus, feed restriction and changing lightering regimes have become the most common commercial conducts employed to reduce the incidence of ascites in broilers4. Both treatments slow down early growth and, unfortunately, they may not produce the same effects in broilers at high altitude. When birds were grown in a hypobaric chamber, ascites incidence increased while the overall growth rate of the birds was decreased3. Thus, alternative measures need to be developed to deal with ascites in broilers at high altitude.

A fast adaptation to high altitude conditions by broiler chickens is required to deal with hypoxia. This adaptation could be facilitated by adaptogens, which have to meet certain criteria proposed by Brekhman and Dardymov (1969)11. Rhodiola, a genus of perennial herbaceous plants in the family Crassulaceae, have been proposed as an adaptogen12. Rhodiola, known as “arctic root” or “golden root”, is able to increase resistance to a variety of stressors12. They have long been used in the treatment of long-term illness and weakness in people in Tibet for over 1000 years. Recent pharmacological studies have shown that Rhodiola possesses many health benefits such as ability to reduce fatigue13, is cytoprotective14, is anti-oxidative and can mitigate free radicals14,15, has immunomodulating properties16,17, is anti-hypoxia18 and can prevent altitude sickness12. Nevertheless, Rhodiola as an adaptogen has not been used in broilers raised in a hypoxic environment. Therefore, the objective of this research was to determine the effects of Rhodiola roots on production performance and health parameters of broilers raised at high altitude.


Bird Performance

There were no significant differences in BW (body weight) at d14 among the three treatment groups. However, the BW of broilers fed the High-R diet (basal diet + 1.5% R. crenulata) was significantly lower at d28 and 42 (p = 0.003 and 0.019, respectively) as compared to birds fed the Low-R (basal diet + 0.5% R. crenulata) and CTL (basal diet) diets (Table 1). In comparison to the CTL diet, High-R diet significantly decreased ADFI (average daily feed intake) at all three 2-week periods (p = 0.047 at d14, 0.044 at d28 and 0.036 at d42). In comparison with the Low-R diet group, the High-R diet significantly decreased ADFI during the first two 2-week periods (p = 0.047). However, there were no significant differences in BW, ADFI and FCR (feed conversion ratio) between the CTL and the Low-R groups. The High-R treatment significantly reduced total feed intake during the six week period as compared with the other two treatments (p = 0.010). There were no significant differences in FCR among all three groups throughout the study.

Table 1: Effects of Rhodiola on production performance of broiler chickens at high altitude


As shown in Figure 1, there were no significant differences in ascites induced mortality among the three groups at all time periods. In addition, there were no significant differences of non-ascites induced mortality and total mortality between the CTL and the High-R groups. On the other hand, the Low-R diet significantly decreased non-ascites induced mortality and total mortality during all three 2-week periods (p = 0.006) (Figure 1).

Figure 1: Effects of Rhodiola on mortality (ascites induced or non-ascites induced) of broiler chickens at high altitude.
Figure 1

C: basal diet; L: CTL + 0.5% R.crenulata; H: CTL + 1.5% R.crenulata. * indicate the significant difference of the total mortality in comparison with the control group, while different litters (a,b) mean significant differences in non-ascites induced mortality in comparison with the control group.

Organ index and blood parameters

There were no significant differences among the RV/TV (right ventricle weight/total ventricle weight) ratios of all three groups. Similarly, there was no change in TV/BW (total ventricle weight/body weight), except on 28 d, between the High-R and the Low-R groups. Compared to CTL, Low-R diet significantly decreased THW/BW (total heart weight/body weight) at d42 (p = 0.043). At the same time and as compared with the Low-R diet, the High-R diet significantly increased THW/BW (p = 0.043). While there was no significant difference in the LW/BW ratio on d14, the High-R group had a significantly higher LW/BW (lung weight/body weight) ratio than the control on d28 and d42 (p = 0.035 and 0.004, respectively) (Table 2).

Table 2: Effects of Rhodiola on cardiac and lung indices and blood parameters of broiler chickens at high altitude

As shown in Table 2, the High-R diet significantly increased blood RBC (red blood cell) counts, HGB (hemoglobin) levels and HGT (hematocrit) values on d28 in comparison with CTL and Low-R diets (p = 0.001, 0.001 and 0.002, respectively). In addition, the HGT value in Low-R group was significantly higher than values in the CTL group on d14 and d28 (p = 0.033 and 0.002, respectively). There were no significant differences in RBC counts, HGB levels and HGT values among all groups on d42.

Histological Parameters

As shown in Table 3, the High-R diet significantly decreased the height of duodenum villi on d28 and d42 (p = 0.003 and 0.001, respectively) and jejunum villi on d42 (p = 0.029) when compared with the CTL and Low-R diets. At the same time, the High-R diet significantly decreased the height of ileum villi on d28 when compared with the Low-R diet (p = 0.021).

Table 3: Effects of Rhodiola on villi height of broiler chickens at high altitude μm

The effect of the three diets on crypt depth is presented in Table 4. In comparison with the CTL diet, the High-R diet significantly reduced duodenum crypt depth on d28 and d42 (p = 0.001 and 0.037, respectively), jejunum crypt depth on d14, d28 and d42 (p = 0.046, 0.044 and 0.031, respectively) and ileum crypt depth on d28 only (p = 0.044). The Low-R diet did not have any significant effects on crypt depth when compared with the CTL diet at all periods. The significant difference of crypt depth between the Low-R and the High-R diets was also observed for duodenum crypt depth on d42 (p = 0.001), for jejunum crypt depth on d28 and d42 (p = 0.044 and 0.031, respectively) and for ileum crypt depth on d28 (p = 0.044).

Table 4: Effects of Rhodiola on crypt depth of broiler chickens at high altitude μm


Our results support the notion that high altitude may reduce body weight. The final bodyweight of broilers in the CTL group at 2986m above sea level was 1347 g. This is approximately 35.5% lower than the expected growth performance of 2088 g at 42 d based on NRC (1994)22, despite the fact that broilers were fed a diet containing nutrients at NRC22 recommended levels. Our result is also in general agreement with the report of Balog et al (2000)3, who found that the final bodyweight of broilers raised in a hypobaric chamber (simulated 2900 m above sea level) was approximately 1650 g. The observed reduced body weight at high altitude could be due to a reduction in nutritional energy intake, a reduction in intestinal energy uptake as a result of impaired intestinal function and increased energy expenditure23. The ADFI was decreased by 30.8% in our control group as compared to NRC expected feed intake rate (NRC, 1994)22. Similarly, Westerterp et al. (2006)24 suggested that energy intake is the dominant determinant of body weight loss for humans under hypoxic conditions at high altitude. In addition, villi height and crypt depth were reduced in our study as compared with chickens raised at low altitude21, suggesting that absorption of nutrients at high altitude could be compromised. This observation is also supported by the finding of Santos et al (2005)5, who reported that simulated high altitude decreased gut development of broilers. Compromised intestinal development could be associated with decreased efficiency of nutrient absorption25. In comparison with the control group, the low level of R. crenulata had no effect on production parameters (BW, ADG, ADFI, FCR), but the high level of R. crenulata decreased the production performance of broilers, presumably due to the reduced feed intake caused by the poor taste of the feed.

The survival rate of lowland broilers appears to reduce when they are reared at high altitude such as in Tibet. Lowland chickens are susceptible to pulmonary hypertension due to the inadvertent consequence of selective breeding for rapid body growth and better feed conversion26. For many years, ascites has been a major cause of illness and death in meat-type chickens reared at high altitude (above 3,500 m)7. At high altitude, hypoxia forces the heart to greater activities due to pulmonary blood vessel constriction, which may result in a higher cardiac output, right ventricular hypertrophy and ascites7. Therefore, mortality in this study was categorized into ascites-induced and non-ascites-induced death. In addition to clinical symptoms such as serous fluid accumulation in the abdominal cavity4, hematological and anatomical changes were used to detect ascites27,28. An increase in the RV/TV ratio indicates the onset of pulmonary hypertension and ascites syndrome29,30,31,32. Hematocrit is another common measure of ascites development. Over 10% of ascites induced mortality in this study and the results of Özkan et al. (2010)4 clearly show that the hypobaric birds exhibited a significantly greater incidence of ascites. Based on our results, R. crenulata did not have anti-ascites potential under the conditions of this study.

The surprising and inspiring finding from this study was that the Low-R diet significantly reduced non-ascites induced mortality. However, whether the reduction was at least partially caused by higher HGT values on day14 and d28 is not clear. The High-R diet significantly increased blood RBC counts, HGB levels and HGT values on d28 in comparison with CTL and Low-R diets. However, the high level of R. crenulata affected the production parameters but did not improve the mortality rate. This could be caused by reduced feed intake and mal-absorption of nutrients indicated by compromised gut development. R. crenulata has a special smell that affects the palatability of feed when large amounts are added. Extracts are being considered for future research, on the condition that it has to be cost-effective. The components of R. crenulata that are responsible for our findings are elusive. Yang et al. (2012)33 reported the isolation of more than 100 compounds from Rhodiola, including phenols and their corresponding glycosides, cyanophoric glycosides, terpenoids, and flavonoids. Most studies for pharmacological functions of Rhodiola have used either whole parts of Rhodiola34 or extracts of Rhodiola17,18,35. Only a few studies have used purified components to test the pharmacological functions of R. crenulata in mostly in vitro experiments. For example, Chen et al (2012)36 found that four water-soluble phenylpropanoid compounds obtained from R. crenulata (p-hydroxyphenacyl-β-D-glucopyranoside, salidroside 2-(4-hydroxyphenyl)-ethyl-O-β-D-glucopyranosyl-6-O-β-D-glucopyranoside, and tyrosol) exhibited radical scavenging activities against 2,2-diphenyl-1-picrylhydrazy (DPPH) in vitro. Lee et al. (2013)37 found that R. crenulata extract and its bioactive components, salidroside and tyrosol, could maintain sodium transport via the preservation of Na, K-ATPase under hypoxia environment in vitro. Purified epicatechin-(4β, 8)-epicatechin gallate (B2-3′-O-gallate), epicatechin gallate (ECG) and 2-(4-hydroxyphenyl) ethyl 3,4,5-trihydroxybenzoate (HETB) from R. crenulata showed a strong α-glucosidase-inhibitory effect38. Similarly, both 4′-hydroxyacetophenone and epicatechin-(4β,8)-epicatechin gallate (B2−3′-O-gallate) inhibited xanthine oxidase (XO) activity, while salidroside and p-tyrosol did not show significant inhibitory effects on XO at 30 μM39. The R. crenulata components responsible for mitigating hypoxia induced pulmonary arterial pressure in this study are not clear. Therefore, more in-depth research must be carried out to elucidate key bioactive components and uncover definite mechanisms responsible for the adaptogenic potential of high altitude raised broilers observed in the present study. Although more research needs to be carried out before R. crenulata can be used in poultry production in Tibet, our findings lay a significant foundation for future studies.


Bird Husbandry

All experimental protocols used in this experiment were in accordance with those approved by the Northwest Agriculture and Forestry (A&F) University Institutional Animal Care and Use Committee (protocol number NWAFAC1008). A previous study has shown that ascites associated mortality in male broilers was higher (13.8%) than in female broilers (8.6%) under high altitude4. So to better create an ascites model that avoids sex difference in ascites associated mortality, hatched 1-d-old healthy Arbor Acres male broilers (n = 270) were obtained from a commercial hatchery at Chengdu (average altitude 500 m above sea level) and transported to the experimental farm of Tibet Agricultural and Animal Husbandry College (average altitude 2986 m above sea level) by air. Chicks were randomly allocated by body weight to 3 treatments (15 birds per cage with 6 cages per treatment) according to a completely randomized design. All chicks had similar initial weights (45.9 ± 0.8 g). Birds were reared in three layer metal cages, with an average stocking density of 16.7 birds per square meter from d1 to d14. Bird densities from d14 to d42 were 8.3 birds per square meter. The brooding temperature was 31 to 33°C during the first week and gradually decreased to 23°C by d21 until the end of the experiment. Daily fluorescent illumination was applied for 23 h with 1 h of dark throughout the experimental period of 42 d.

Experimental Diets

Diets, in crumble form, included a starter diet (12.6 MJ metabolizable energy/kg of diet, 220 g/kg crude protein) from d1 to d21 and a grower diet (13 MJ metabolizable energy/kg of diet, 200 g/kg crude protein) from d22 to d42. The nutrient contents of the diets used in this study met or exceeded the National Research Council (1994) requirements. The control birds were fed the basal diet alone while birds on other treatments received the basal diet supplemented with 0.5% (Low-R diet) or 1.5% (High-R diet) Rhodiola crenulata (R. crenulata). There are 32 Rhodiola species in Tibet. Among these species, R. crenulata is widely used in Tibet to prevent high altitude sickness in humans. In addition, R. crenulata has been successfully cultivated by a botanist of Tibet Agricultural and Animal Husbandry College and the major bioactive components such as salidroside, tyrosol and flavonoid compounds are similar to those of wild R. crenulata (data not published). For this experiment, R. crenulata was purchased from the Tibetan Traditional Medical Hospital and was characterized by the botanist in the college. The roots of R. crenulata were used in this study because they are rich in biologically active compounds such as salidroside and tyrosol40,41,42. Dried roots of R. crenulata were crushed using a laboratory blender before mixing into the feed. The concentrations of major effective constituents in R. Crenulata (flavonoids, phenylpropanoids, and organic acids) measured by high-performance liquid chromatography were 7.55 mg/g for salidroside, 3.72 mg/g for tyrosol, 1.93 mg/g for gallic acid, 1.77 mg/g for rhodionin and 1.01 mg/g for rhodiosin. Feed and water were available at all times.

Production Performance and Health Parameters

Birds were group-weighed at d14, d28 and d42 by cage and average daily gain (ADG) was calculated. Feed intake (FI) was determined weekly and feed consumption (FC) per bird (g/bird) was calculated by dividing the total FC of each cage by the actual number of birds in that cage. The feed conversion ratio (FCR) was determined as the FC per BW gain (g/g) for each cage in each period. Mortality was recorded daily. All dead birds during the experimental period were necropsied to identify ascites related mortality by characteristic symptoms, such as the presence of ascites fluid in the abdominal cavity, right ventricular dilation (RV/TV > 0.29), hydropericardium, and vascular congestion19. When none of the symptoms above occurred in a dead bird, the death was categorized as a non-ascites induced death. At d14, 28 and 42, two birds per cage (n = 12/treatment) were randomly selected and individually weighed. They were killed by cervical dislocation after taking blood samples from the heart. Hearts and lungs were thereafter removed and weighed to the nearest 0.1 g. The heart was resected and the atria were removed to the plane of the atrial ventricular valves followed by weighing the total ventricles (TV). The right ventricular (RV) wall was weighed after it was dissected free of the left ventricle (LV) and septum. Heart and lung weight relative to BW (g/100 g of BW) and the RV/TV ratio were calculated20.

Blood samples from all birds were analyzed for red blood cell (RBC) counts, hemoglobin (HGB) levels and hematocrit (HGT) values. These parameters were determined by an automatic blood analyzer (XFA6000, Pulang Company, Nanjing, China) that had been standardized for analyses of chicken blood.

Gut Morphology

At 14, 28 and 42 d of age, 2 birds per treatment cage (n = 12/treatment) were randomly selected and sacrificed. Segments (1 cm) of duodenum (2 cm from gizzard), jejunum (adjacent to Meckel's diverticulum), and ileum (adjacent to cecal tonsils) were dissected, washed in physiological saline solution, and fixed in 10% buffered formalin21. For each intestinal segment, a 6-μm section was placed onto a glass slide and stained with hematoxylin and eosin for evaluation of villi height and crypt depth.

Statistical analyses

Data were analyzed by the SPSS 13.0 software for windows (SPSS, Chicago, IL). Comparisons between groups were performed using one-way ANOVA followed by the Duncan test. For mortality, a χ2 analysis was performed for each group. Differences are considered statistically significant at the level of p < 0.05 and data are presented as means ± S.D.


  1. 1.

    , , & Blood characteristics for high altitude adaptation in Tibetan chickens. Poult Sci. 86, 1384–1389 (2007).

  2. 2.

    & Taurine, cardiopulmonary hemodynamics, and pulmonary hypertension syndrome in broilers. Poult Sci. 80, 1607–1618 (2001).

  3. 3.

    et al. Ascites syndrome and related pathologies in feed restricted broilers raised in a hypobaric chamber. Poult Sci. 79, 318–323 (2000).

  4. 4.

    et al. The effects of feed restriction and ambient temperature on growth and ascites mortality of broilers reared at high altitude. Poult Sci. 89, 974–985 (2010).

  5. 5.

    et al. Effect of prebiotic on gut development and ascites incidence of broilers reared in a hypoxic environment. Poult Sci. 84, 1092–1100 (2005).

  6. 6.

    , , & Effect of dietary aspirin on ascites in broilers raised in a hypobaric chamber. Poult Sci. 79, 1101–1105 (2000).

  7. 7.

    Ascites in poultry. Avian Pathol. 22, 419–454 (1993).

  8. 8.

    , , , & Effect of chronic hypoxia during the embryonic development on the physiological functioning and on hatching parameters related to ascites syndrome in broiler chickens. Avian Pathol. 33, 558–564 (2004).

  9. 9.

    & World broiler ascites survey 1996. Poultry International. 36, 16–30 (1997).

  10. 10.

    , & Broiler ascites syndrome: collateral damage from efficient feed to meat conversion. Vet J. 197, 169–174 (2013).

  11. 11.

    & New substances of plant origin which increase nonspecific resistance. Annu Rev Pharmacol. 9, 419–430 (1969).

  12. 12.

    Rhodiola rosea: a possible plant adaptogen. Altern Med Rev. 6, 293–302 (2001).

  13. 13.

    , , , & Dietary supplement with a combination of Rhodiola crenulata and Ginkgo biloba enhances the endurance performance in healthy volunteers. Chin J Integr Med. 15, 177–183 (2009).

  14. 14.

    et al. Cytoprotective and antioxidant activity of Rhodiola imbricata against tert-butyl hydroperoxide induced oxidative injury in U-937 human macrophages. Mol Cell Biochem. 275, 1–6 (2005).

  15. 15.

    et al. In vitro protective effect of Rhodiola rosea extract against hypochlorous acid induced oxidative damage in human erythrocytes. Biofactors. 20, 147–159 (2004).

  16. 16.

    et al. Aqueous extract of Rhodiola imbricata rhizome stimulates proinflammatory mediators via phosphorylated IκB and transcription factor nuclear factor-κB. Immunopharmacol Immunotoxicol. 28, 201–212 (2006).

  17. 17.

    , & Anti-cellular and immunomodulatory potential of aqueous extract of Rhodiola imbricata rhizome. Immunopharmacol Immunotoxicol. 34, 513–518 (2012).

  18. 18.

    et al. The Extract of Rhodiolae crenulatae radix et Rhizoma induces the accumulation of HIF-1α via blocking the degradation pathway in cultured kidney fibroblasts. Planta Med. 77, 894–899 (2011).

  19. 19.

    , & Evaluation of growth rate, body weight, heart rate, and blood parameters as potential indicators for selection against susceptibility to the ascites syndrome in young broilers. Poult Sci. 86, 621–629 (2007).

  20. 20.

    et al. Gene expression of endothelin-1 and its receptors in the heart of broiler chickens with T3-induced pulmonary hypertension. Res Vet Sci. 91, 370–375 (2011).

  21. 21.

    , & Effects of diets containing different concentrations of mannanoligosaccharide or antibiotics on growth performance, intestinal development, cecal and litter microbial populations, and carcass parameters of broilers. Poult Sci. 88, 2262–2272 (2009).

  22. 22.

    National Council Research. Nutrient Requirements of Poultry, 9th revised edition. National Academy Press, Washington, DC. (1994).

  23. 23.

    & Hypoxia, energy balance and obesity: from pathophysiological mechanisms to new treatment strategies. Obes Rev. 14, 579–592 (2013).

  24. 24.

    & Body mass regulation at altitude. Eur J Gastroenterol Hepatol. 18, 1–3 (2006).

  25. 25.

    , & Developmental regulation of intestinal angiogenesis by indigenous microbes via Paneth cells. Proc Natl Acad Sci. 99, 15451–15415 (2002).

  26. 26.

    , & Ascites in broiler chickens: exogenous and endogenous structural and functional causal factors. World's Poult. Sci. 56, 367–377 (2000).

  27. 27.

    , & Studies on an ascitic syndrome in young broilers. 1. Haematology and pathology. Avian Pathol. 15, 511–524 (1986).

  28. 28.

    , & Haematology and morphological changes in young broiler chicks with experimentally induced hypoxia. Res Vet Sci. 43, 331–338 (1987).

  29. 29.

    , & Effect of chronic hypoxia on the pulmonary arterial blood pressure of the chicken. Am J Physiol. 214, 1438–1442 (1968).

  30. 30.

    , , & High altitude induced pulmonary hypertension and right heart failure in broiler chickens. Res Vet Sci. 16, 370–374 (1974).

  31. 31.

    & Pulmonary hypertension syndrome associated with ascites in broilers. Vet Rec. 119, 94–94 (1986).

  32. 32.

    Hypoxic ascites in broilers: a review of several studies done in Colombia. Avian Dis. 31, 658–661 (1987).

  33. 33.

    , , , & Lignans from the Root of Rhodiola crenulata. J Agric Food Chem. 60, 964–972 (2012).

  34. 34.

    et al. Rhodiola crenulata root ameliorates derangements of glucose and lipid metabolism in a rat model of the metabolic syndrome and type 2 diabetes. J Ethnopharmacol. 142, 782–788 (2012).

  35. 35.

    , & Evaluation of Rhodiola crenulata and Rhodiola rosea for management of type II diabetes and hypertension. Asia Pac J Clin Nutr. 15, 425–432 (2006).

  36. 36.

    et al. Isolation, identification and antioxidative capacity of water-soluble phenylpropanoid compounds from Rhodiola crenulata. Food Chem. 134, 2126–2133 (2012).

  37. 37.

    et al. Rhodiola crenulata and its bioactive components, salidroside and tyrosol, reverse the hypoxia-induced reduction of plasma-membrane-associated Na, K-ATPase expression via inhibition of ROS-AMPK-PKCξ pathway. Evid Based Complement Alternat Med. 2013, 284150 (2013).

  38. 38.

    , & Isolation and characterization of α-glucosidase inhibitory constituents from Rhodiola crenulata. Food Res Int. 57, 8–14 (2014).

  39. 39.

    , , & Inhibition of xanthine oxidase by Rhodiola crenulata extracts and their phytochemicals. J Agric Food Chem. 62, 3742–3749 (2014).

  40. 40.

    , , & Determination of p-tyrosol and salidroside in three samples of Rhodiola crenulata and one of Rhodiola kirilowii by capillary zone electrophoresis. Anal Bioanal Chem. 377, 370–374 (2003).

  41. 41.

    , , & Bioactive constituents from Chinese natural medicines. XXVIII. Chemical structures of acyclic alcohol glycosides from the roots of Rhodiola crenulata. Chem Pharm Bull. 56, 536–540 (2008).

  42. 42.

    & Identification and comparative determination of rhodionin in traditional tibetan medicinal plants of fourteen Rhodiola species by high-performance liquid chromatography-photodiode array detection and electrospray ionization-mass spectrometry. Chem Pharm Bull. 56, 807–814 (2008).

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This work was supported by funding from the China QianRen program to X.Z. and a youth fund of Agricultural and Animal Husbandry College of Tibet University to L.L. Suggestions by Dr. Eveline Ibeagha-Awemu to improve the manuscript are gratefully appreciated.

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  1. College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, People's Republic of China

    • Long Li
    •  & Xin Zhao
  2. College of Animal Science, Agricultural and Animal Husbandry College of Tibet University, Nyingchi, Tibet, People's Republic of China

    • Long Li
    •  & Honghui Wang
  3. Department of Animal Science, McGill University, 21, 111 Lakeshore, Ste. Anne de Bellevue, Quebec, Canada, H9X 3V9

    • Xin Zhao


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L.L. and X.Z. contributed to the initial design of this experiment. L.L. and W.H. performed the experiment. L.L. analyzed the data. L.L. and X.Z. prepared the manuscript of this publication.

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The authors declare no competing financial interests.

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Correspondence to Xin Zhao.

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