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Amino Acids

, Volume 42, Issue 6, pp 2481–2489 | Cite as

Importance of amino acid composition to improve skin collagen protein synthesis rates in UV-irradiated mice

  • Hitoshi MurakamiEmail author
  • Kazutaka Shimbo
  • Yoshiko Inoue
  • Yoshinobu Takino
  • Hisamine Kobayashi
Open Access
Original Article

Abstract

Skin collagen metabolism abnormalities induced by ultraviolet (UV) radiation are the major causes of skin photoaging. It has been shown that the one-time exposure of UV irradiation decreases procollagen mRNA expression in dermis and that chronic UV irradiation decreases collagen amounts and induces wrinkle formation. Amino acids are generally known to regulate protein metabolism. Therefore, we investigated the effects of UV irradiation and various orally administered amino acids on skin collagen synthesis rates. Groups of 4–5 male, 8-week-old HR-1 hairless mice were irradiated with UVB (66 mJ/cm2) twice every other day, then fasted for 16 h. The fractional synthesis rate (FSR; %/h) of skin tropocollagen was evaluated by incorporating l-[ring-2H5]-phenylalanine. We confirmed that the FSR of dermal tropocollagen decreased after UVB irradiation. The FSR of dermal tropocollagen was measured 30 min after a single oral administration of amino acids (1 g/kg) to groups of 5–16 UVB-irradiated mice. Branched-chain amino acids (BCAA, 1.34 ± 0.32), arginine (Arg, 1.66 ± 0.39), glutamine (Gln, 1.75 ± 0.60), and proline (Pro, 1.48 ± 0.26) did not increase the FSR of skin tropocollagen compared with distilled water, which was used as a control (1.56 ± 0.30). However, essential amino acids mixtures (BCAA + Arg + Gln, BCAA + Gln, and BCAA + Pro) significantly increased the FSR (2.07 ± 0.58, 2.04 ± 0.54, 2.01 ± 0.50 and 2.07 ± 0.59, respectively). This result suggests that combinations of BCAA and glutamine or proline are important for restoring dermal collagen protein synthesis impaired by UV irradiation.

Keywords

Amino acids Skin collagen Protein synthesis rate UV-irradiated rat 

Abbreviations

UV

Ultraviolet

FSR

Fractional synthesis rate

AP-1

Activator protein 1

TGF-b

Transforming growth factor-beta

EGF

Epidermal growth factor

IL1

Interleukin 1

TNF-a

Tumor necrosis factor-alpha

mTOR

Mammalian target of rapamycin

p70S6K

70 kDa ribosomal protein S6 kinase

4E-BP1

Eukaryotic initiation factor-binding protein 1

GAPP

Glutamate-dependent protein phosphatase

BCAA

Branched-chain amino acids

Leu

Leucine

Ile

Isoleucine

Val

Valine

Gln

Glutamine

Arg

Arginine

Pro

Proline

EAA

Essential amino acids

Glu

Glutamate

DW

Distilled water

Introduction

Skin aging, especially wrinkling and sagging, is induced by several factors, including ultraviolet (UV) irradiation, dryness, chemical stimulation, malnutrition, and exposure to activated oxygen species (Rittie and Fisher 2002). In particular, UV radiation is a potent agent of skin aging, and many reports suggest that chronic UV irradiation damages the skin protein and induces wrinkle formation in humans and animals (Boyer et al. 1992; Fisher et al. 2000, 2001; Rittie and Fisher 2002; Takema et al. 1996). Dermal collagen is a major component of skin dermis and is necessary to maintain skin structure. UV irradiation stimulates several factors, such as AP-1, TGF-β, EGF, IL1, and TNF-α, that affect collagen metabolism. Fischer has reported that in humans, procollagen mRNA levels are decreased and matrix metalloprotease mRNA levels are increased by single UV irradiation (Fisher 2005; Fisher et al. 2000, 2001). Takema found that in mice, chronic UV irradiation decreases the dermal collagen protein, resulting in wrinkle formation (Takema et al. 1996). These articles indicated that the decrease in dermal collagen protein resulting from chronic UV stimulation is one of the main causes of skin aging (Rittie and Fisher 2002). Cellular protein levels are regulated by protein turnover processes, such as protein synthesis and breakdown. However, there has been little study of the impact of UV irradiation on dermal collagen protein synthesis rates. To maintain steady dermal collagen levels, it is important to correct changes in the protein turnover rate induced by UV irradiation.

Amino acids are protein substrates and regulators of protein metabolism and are highly safe for humans. In an in vitro study, Bellon et al. (1995, 1987) found that glutamine increases procollagen mRNA levels and collagen content, and suggested that de novo proline synthesis from glutamine is important for collagen synthesis. Proline and its precursors, glutamate and pyrroline-5-carboxylate, increase collagen synthesis in human fibroblast cells (Karna et al. 2001). Some amino acids, such as arginine (Shi et al. 2003; Stechmiller et al. 2005) and ornithine (Shi et al. 2002), and amino acid mixtures (Badiu et al. 2010; Corsetti et al. 2010) enhance wound healing in rats. Zhang also indicated that leucine supplementation has an anabolic effect on protein metabolism in skin wounds in rabbits (Zhang et al. 2004). However, few studies have focused on amino acids’ ability to restore dermal collagen synthesis after UV irradiation. UV irradiation and wounds provoke different healing responses (Fisher 2005; Johnstone and Farley 2005).

Consequently, the present study was performed to investigate the effects of UVB irradiation on the FSR of mouse skin collagen and to investigate which amino acids can correct these FSR changes.

Methods

Animals

This study was approved by the Institutional Animal Care and Use Committee of Ajinomoto Co., INC. Nine-week-old male HR-1 hairless mice (Sankyo lab service Co. Japan) were housed in a temperature-controlled room with a 12-hour light and dark cycle. The animals were given standard commercial chow (CR-F1, Charles River, Japan) and water ad libitum.

UV irradiation

UVB radiation was generated with a bank of six sun lamps (FL20S-E-30/DMR, 20W, peak emission near 305 nm; Toshiba Medical Supply, Tokyo, Japan). The minimal erythema dose (MED) determined 24 h after UV irradiation was 66 mJ/cm2.

Experimental design

The first experiment investigated the effect of UVB irradiation on the FSR of skin tropocollagen. Mice (four or five in each group) were irradiated with UVB (66 mJ/cm2) on the dorsal skin one, two, three, or four times at a one-day intervals. The FSR was evaluated using the flooding dose method described by Garlick and McNurlan (1998). After 16 h of fasting after the last UV irradiation, the mice were injected in the tail veins with flooding doses of phenylalanine (1.5 mmol/kg body weight) containing l-[ring-2H5]-phenylalanine (50 mol percent excess, Cambridge isotope, Cambridge, MA). The mice were killed by decapitation 5 min after the phenylalanine injection. Blood was then collected from the necks, and the dorsal skins were removed. Subcutaneous skin fat was immediately removed, and the dermis was frozen in liquid nitrogen and stored at −80°C. Blood was separated from plasma by centrifugation at 3,000g for 15 min at 4°C, and the plasma was stored at −80°C.

The second experiment investigated the effect of orally administered amino acids on the skin tropocollagen FSR of UV-irradiated mice. The mice’s dorsal skins were irradiated with UVB (66 mJ/cm2) twice every other day. After 16 h of fasting, different amino acid solutions (1 g/ml/kg body weight) were orally administered by gastric tube to groups of 5–16 mice. The amino acid amount in the solutions was an amount commonly used in animal experiments to investigate acute amino acid effects (Farges et al. 1999; Smriga and Torii 2003). The compositions of the solutions are shown in Table 1 (all amino acids were manufactured by Ajinomoto Co., Inc.). Twenty-five minutes after the solutions were administered, the mice were injected with flooding doses of phenylalanine, and skin and blood were collected as described above.
Table 1

Compositions of amino acid solution

 

Glutamine (Gln) (g)

Arginine (Arg) (g)

Proline (Pro) (g)

Branched-chain amino acids (BCAA) (g)

Arg + Gln (RQ) (g)

BCAA + Arg + Gln (BCAARQ) (g)

BCAA + Arg (BCAAR) (g)

BCAA + Gln (BCAAQ) (g)

BCAA + Pro (BCAAP) (g)

BCAA + Glu (BCAAE) (g)

Essential amino acids (EAA) (g)

Threonine

0.150

Phenylalanine

0.171

Lysine

0.127

Histidine

0.111

Methionine

0.032

Isoleucine

0.250

0.125

0.125

0.125

0.125

0.125

0.103

Leucine

0.500

0.250

0.250

0.250

0.250

0.250

0.190

Valine

0.250

0.125

0.125

0.125

0.125

0.125

0.117

Glutamine

1.000

0.500

0.250

0.500

Arginine

1.000

0.500

0.250

0.500

Glutamate

0.500

Proline

1.000

0.500

Total (g/kg BW)

1.000

1.000

1.000

1.000

1.000

1.000

1.000

1.000

1.000

1.000

1.000

Sample preparation

Tropocollagen was extracted using a modification of Volpi’s method (Volpi et al. 2000). Briefly, approximately 0.5 g of dorsal skin was homogenized on ice in Buffer A (10 ml/g of skin), a pH 7.4 buffer containing 150 mM NaCl, 50 mM Tris–HCl, 2 mM EDTA, 1 mM phenylmethylsulfonyl fluoride, 2 mM N-ethylmaleimide, and 0.2 mM 2-aminopropionitrile. The homogenized sample was shaken overnight at 4°C, and then centrifuged at 7,500g for 10 min at 4°C. The supernatant was filtered with a 75-mm mesh, brought to 4.5 M with NaCl, and shaken for 5 h. The solution was centrifuged at 70,000g for 30 min at 4°C. The precipitate was dissolved in Buffer B, a pH 7.6 buffer containing 200 mM NaCl, 50 mM Tris–HCl, and 2 mM EDTA, and the solution was dialyzed in Buffer B for 2 h. This dialyzed sample, which included large amounts of skin tropocollagen, was hydrolyzed with hydrochloric acid for 16 h at 90°C, and the hydrolysate was used to measure isotope incorporation rates in the tropocollagen. To confirm the purity of the extracted tropocollagen, the dialyzed sample was subjected to SDS-PAGE (E-pagell, gradient gel 5–20%, ATTO, Japan) using a molecular mass standard (Bio-Rad, USA). Two wells were loaded with same amounts of the same samples. One was stained with Coomassie Brilliant Blue to detect proteins, and the other was blotted on nitrocellulose to identify collagen proteins using Western blotting with a mixture of antibody anti-collagen types I, III, and VII (Calbiochem, USA).

Approximately 0.04 g of dermal skin was homogenized with 15% sulfosalicylic acid, and the homogenate was centrifuged at 10,000g for 10 min at 4°C. The supernatant was used as skin tissue fluid. The precipitate was hydrolyzed in 2 ml of 6 N HCl at 90°C for 16 h and was used as mixed skin protein.

Amino acids that included hydrolysates and tissue fluid were purified by cation exchange chromatography (Dowex 50W 8X; Bio-Rad Laboratories, USA) and dried in a rotary evaporator (Nakajima corp., Japan).

Analysis

Phenylalanine enrichment (E (skin free)) in the tissue fluid was determined by its tert-butyldimethylsilyl (t-BDMS, Pierce, USA) derivatization. Gas chromatography–mass spectrometry was used to monitor Ions 336 and 341 in the electron impact mode (GC–MS; 6890 GC system and 5473 Network mass selective detector, Agilent, USA). Phenylalanine enrichment in the tropocollagen and mixed skin protein samples (E (tropocollagen), E (mixed skin)) was determined by measuring their AQC-detergent (Waters, USA) derivatization using liquid chromatography–mass spectrometry to monitor ions 336 and 341 in the first MS and 171 in the second MS (LC–MS/MS; Prominence HPLC system, Shimazu, Japan and API 3200, Applied Biosystems, USA). Plasma insulin concentrations were measured using a commercial ELISA-kit (Morinaga Institute Biological Science, Japan), and amino acid concentrations were measured with an automatic amino acid analyzer (L-8500, Hitachi, Japan).

Calculation and statistics

The FSR of the skin tropocollagen and mixed skin protein was calculated with the precursor-product model. The precursor represented the free phenylalanine enrichment in the skin tissue fluid, and the product represented the enrichment of the phenylalanine-incorporated skin tropocollagen or mixed skin protein. The FSR was calculated as FSR (%/h) = E (tropocollagen or mixed skin)/(E (skin free) × t) × 100, where t represents the time interval between phenylalanine injection and sampling.

Values are presented as means ± SD. Comparisons with the control group (given distilled water, DW) were made via Dunnett’s test after ANOVA for multiple comparison (JMP, SAS Institute, Cary, NC, USA). Values of P < 0.05 were considered significant.

Results

Skin tropocollagen extracted from the dorsal skin was assayed with Western blotting to confirm its purity. The protein bands of extracted skin tropocollagen separated by SDS-PAGE corresponded to Type I, III, and VII collagen bands (Fig. 1). The purity of the extraction was confirmed as described in a previous article (Volpi et al. 2000).
Fig. 1

SDS-PAGE and Western blot analysis of isolated skin tropocollagen fractions. Type I, III and VII collagen were identified using Western blot, and the purity of extracted collagen was confirmed. sd Standard protein, and TP tropocollagen

The FSR of skin tropocollagen tended to decrease after UVB irradiation, especially for mice that were irradiated twice with a one-day interval between irradiations (Fig. 2). The effect of orally administered amino acid on the FSR in the dermal tropocollagen of UVB-irradiated mice is shown in Fig. 3. Thirty minutes after oral amino acid administration, BCAA + Arg + Gln, BCAA + Gln, BCAA + Pro, and essential amino acids (EAA) significantly increased the FSR of skin tropocollagen compared with the control group (2.04 ± 0.54, 2.01 ± 0.50, 2.07 ± 0.59 and 2.07 ± 0.58%/h, respectively, in amino acid groups compared with DW, 1.47 ± 0.21%/h). However, single amino acids (Arg, Gln or Pro: 1.66 ± 0.39, 1.73 ± 0.67 or 1.45 ± 0.26%/h, respectively) and amino acid mixtures (BCAA, Arg + Gln or BCAA + Glu: 1.30 ± 0.32, 1.72 ± 0.26 or 1.74 ± 0.34, respectively) did not increase the FSR.
Fig. 2

Effect of UVB irradiation on the FSR of skin tropocollagen. Samples were irradiated with UVB one, two, three, or four times at one-day intervals. The FSR of tropocollagen decreased to its minimum value after two UVB irradiations. Values are means ± SD

Fig. 3

Effect of orally administered amino acids on the FSR of skin tropocollagen in UVB-irradiated mice. BCAA + Arg + Gln (BCAARQ), BCAA + Gln (BCAAQ), BCAA + Pro (BCAAP) and an essential amino acid mixture (EAA) significantly increased the FSR of skin tropocollagen 30 min after oral administration, but single amino acids did not increase the FSR. It is necessary to include BCAA in amino acid mixtures to increase the FSR of skin tropocollagen. Values are presented as means ± SD. Comparisons with the control group (DW distilled water) were carried out with a Dunnett’s test after ANOVA for multiple comparison (*P < 0.05)

The effect of oral amino acid administration on the FSRs of mixed skin protein is shown in Fig. 4. The FSRs of mixed skin protein were increased by UVB irradiation. However, oral amino acid administration did not affect the FSRs.
Fig. 4

Effect of orally administered amino acids on the FSR of mixed skin protein in UVB-irradiated mice. The FSR of mixed skin protein, including dermis and epidermis, was increased by UVB irradiation. This suggests that the synthesis rate of keratin, the most abundant protein in epidermis, increases with UVB irradiation. Amino acids did not further increase the FSR of mixed skin protein. Values are presented as means ± SD. Statistical comparisons with the control group (DW, distilled water) was carried out with a Dunnett’s test after ANOVA for multiple comparisons (# P < 0.05)

Plasma insulin concentrations 30 min after oral amino acid administration are shown in Fig. 5. Arg + Gln significantly increased plasma insulin concentrations compared to the DW group (1.14 ± 0.61 vs. 0.56 ± 0.6 nag/ml). However, there was no correlation between plasma insulin concentration and the FSR of skin tropocollagen (r 2 = 0.0049; Fig. 6).
Fig. 5

Plasma insulin concentrations 30 min after oral amino acids administration to UVB-irradiated mice. Arg + Gln (RQ) significantly increased plasma insulin concentrations 30 min after oral administration. However, there was no correlation between plasma insulin concentration and the FSR of skin tropocollagen. We postulate that BCAA + Arg + Gln (BCAARQ), BCAA + Gln (BCAAQ), BCAA + Pro (BCAAP), and the essential amino acids mixture (EAA) increased the FSR of skin tropocollagen independently of insulin. Values are presented as means ± SD. Comparisons with the control group (DW distilled water) were conducted with a Dunnett’s test after ANOVA for multiple comparison (*P < 0.05)

Fig. 6

Correlation between the FSR of tropocollagen and plasma insulin. Multivariate correlation was evaluated between the FSR of tropocollagen and plasma insulin concentration. There was no significant correlation between groups (r 2 = 0.004)

Plasma amino acid concentrations are shown in Table 2. Plasma branched-chain amino acid concentrations increased by approximately five times in the BCAA + Arg + Gln, BCAA + Arg, BCAA + Gln, BCAA + Pro, BCAA + Glu and EAA groups compared with the DW group. Plasma tryptophan, histidine, tyrosine, threonine, serine and especially, glycine concentrations decreased in the groups that received solutions containing BCAA. Plasma proline concentrations increased in the groups that received solutions containing proline and slightly increased in Arg and Arg + Gln groups.
Table 2

Plasma amino acids concentration 30 min after oral amino acids administration in UV-irradiated mice

 

DW

Gln

Arg

Pro

BCAA

RQ

BCAARQ

BCAAR

BCAAQ

BCAAP

BCAAE

EAA

Taurine

66.51 ± 12.26

74.95 ± 11.85*

83.79 ± 2.87

95.66 ± 32.46*

78.49 ± 12.34

71.57 ± 10.72

73.05 ± 8.40

65.80 ± 7.28

63.21 ± 9.53

78.03 ± 17.14

71.12 ± 10.41

60.80 ± 16.37

Aspartic acid

2.65 ± 0.74

3.31 ± 1.60

2.93 ± 2.12

2.83 ± 1.03

1.37 ± 1.04

1.65 ± 2.15

2.02 ± 1.35

2.31 ± 1.17

2.23 ± 1.56

1.61 ± 0.63

4.51 ± 2.86

1.77 ± 1.39

Hydroxy proline

1.71 ± 1.12

1.08 ± 0.92

2.08 ± 0.90

0.89 ± 0.29

0.84 ± 0.17

1.51 ± 0.81

1.69 ± 1.07

0.83 ± 0.50

0.77 ± 0.73

0.98 ± 0.36

0.82 ± 0.84

1.60 ± 0.97

Threonine

15.92 ± 2.54

13.06 ± 2.21

13.64 ± 0.78

14.96 ± 4.91

13.54 ± 3.62

14.30 ± 2.62

11.91 ± 2.99

11.26 ± 2.54

11.00 ± 1.97*

11.91 ± 1.22

11.65 ± 1.66

69.39 ± 16.18*

Serine

12.91 ± 2.20

11.84 ± 2.19

12.22 ± 0.03

12.64 ± 3.77

10.60 ± 1.43

13.26 ± 4.04

10.00 ± 1.73

9.34 ± 0.90*

9.03 ± 2.23*

9.89 ± 1.02*

9.81 ± 1.83

10.50 ± 2.31

Asparagine

4.27 ± 0.60

3.36 ± 0.99

2.72 ± 1.29

3.83 ± 1.18

2.65 ± 1.84*

3.40 ± 1.36

3.53 ± 1.72

3.20 ± 0.60

6.52 ± 1.31

3.24 ± 1.23

2.80 ± 0.79

3.32 ± 1.51

Glutamic acid

8.45 ± 1.70

9.08 ± 2.14

11.10 ± 1.26

11.58 ± 4.04

8.69 ± 1.88

9.44 ± 1.56

8.66 ± 2.96

7.01 ± 1.17

7.14 ± 1.87

8.48 ± 2.56

32.62 ± 6.40*

6.70 ± 2.35

Glutamine

43.24 ± 8.23

60.51 ± 9.40*

43.07 ± 6.04

50.30 ± 14.73

54.11 ± 8.37

48.79 ± 5.79

50.71 ± 3.54

44.44 ± 7.83

53.28 ± 9.62

58.96 ± 9.92*

51.21 ± 3.32

45.98 ± 8.98

Proline

6.97 ± 1.40

7.07 ± 1.68

11.79 ± 1.86

349.95 ± 126.77*

6.19 ± 1.53

11.09 ± 1.94

7.87 ± 1.24

7.03 ± 1.00

6.19 ± 1.59

111.39 ± 32.59*

6.08 ± 1.80

5.92 ± 1.40

Glycine

22.31 ± 2.85

20.03 ± 2.60

22.62 ± 2.51

23.60 ± 6.95

16.85 ± 2.91*

20.21 ± 4.08

16.95 ± 2.78*

15.04 ± 1.92*

15.24 ± 3.30*

17.45 ± 2.73*

17.93 ± 3.63

14.17 ± 3.68*

Alanine

23.85 ± 6.08

21.70 ± 3.65

26.76 ± 1.85

38.02 ± 10.33*

20.75 ± 5.33

28.10 ± 6.76

25.92 ± 5.47

21.80 ± 4.22

23.66 ± 4.47

27.00 ± 6.07

31.12 ± 4.38

28.38 ± 8.21

Citrulline

3.13 ± 0.63

5.13 ± 1.26*

3.14 ± 0.50

3.12 ± 0.97

4.40 ± 0.89

4.18 ± 0.98

6.46 ± 1.32*

5.34 ± 1.15*

5.85 ± 1.15*

4.14 ± 0.32

4.22 ± 0.63

3.47 ± 1.51

Valine

25.67 ± 3.74

29.01 ± 31.83

22.72 ± 1.56

20.54 ± 5.11

250.64 ± 39.37*

23.55 ± 4.15

110.53 ± 19.36*

103.25 ± 18.87*

108.56 ± 18.52*

110.50 ± 14.27*

103.96 ± 11.49*

91.22 ± 20.13*

Cystine

0.14 ± 0.09

0.16 ± 0.04

0.21 ± 0.14

0.22 ± 0.21

0.12 ± 0.17

0.13 ± 0.06

0.18 ± 0.12

0.06 ± 0.10

0.10 ± 0.08

0.05 ± 0.07

0.26 ± 0.13

0.29 ± 0.22

Methionine

5.92 ± 1.25

5.84 ± 1.12

5.61 ± 0.12

5.29 ± 1.52

4.31 ± 1.09

6.63 ± 2.33

3.95 ± 1.01

3.43 ± 0.57*

3.65 ± 1.35

4.00 ± 0.68

3.76 ± 1.60

20.88 ± 4.54*

Isoleucine

11.65 ± 1.85

12.34 ± 13.78

10.83 ± 1.43

8.10 ± 1.60

167.32 ± 43.18*

10.22 ± 2.18

53.99 ± 13.15*

49.50 ± 9.47*

51.61 ± 13.64

56.89 ± 9.60*

49.20 ± 7.84*

38.64 ± 11.33*

Leucine

18.62 ± 3.03

21.30 ± 26.40

17.78 ± 2.99

12.96 ± 3.26

235.13 ± 55.16*

17.96 ± 3.83

100.69 ± 24.50*

92.55 ± 17.63*

93.06 ± 23.57*

101.66 ± 17.17*

88.69 ± 14.53*

66.55 ± 18.74*

Tyrosine

27.12 ± 6.73

27.50 ± 5.45

29.72 ± 8.87

26.22 ± 8.04

19.87 ± 1.84*

25.46 ± 6.89

19.72 ± 4.15

19.57 ± 4.21*

20.79 ± 4.78

24.15 ± 4.74

19.06 ± 5.99*

30.71 ± 5.61

Phenylalanine

138.61 ± 30.89

131.36 ± 24.81

161.16 ± 39.97

130.44 ± 39.62

158.48 ± 26.45

115.30 ± 49.57

128.17 ± 48.57

133.10 ± 36.30

152.94 ± 34.87

146.42 ± 10.77

143.54 ± 12.02

158.44 ± 37.10

Tryptophan

8.10 ± 1.31

7.72 ± 1.17

7.17 ± 2.32

7.34 ± 2.75

5.62 ± 1.97*

6.15 ± 1.35

5.37 ± 1.56*

6.54 ± 1.35

7.17 ± 1.53

6.27 ± 1.27

7.16 ± 1.81

5.26 ± 2.33

Ornithine

9.86 ± 2.61

9.90 ± 2.34

135.10 ± 13.72*

11.14 ± 3.81

2.98 ± 1.82

85.43 ± 32.27*

68.85 ± 17.09*

115.29 ± 29.34*

22.80 ± 43.34

7.85 ± 0.70

8.72 ± 2.79

7.77 ± 3.32

Lysine

23.42 ± 3.99

21.48 ± 3.61

24.87 ± 1.88

17.27 ± 4.72

21.16 ± 4.51

30.10 ± 7.71

20.55 ± 3.29

20.94 ± 3.27

18.38 ± 2.88

18.01 ± 2.62

19.28 ± 3.66

61.84 ± 20.44*

1Methyl histidine

0.20 ± 0.07

0.21 ± 0.13

0.13 ± 0.18

0.11 ± 0.13

0.09 ± 0.13

0.20 ± 0.05

0.13 ± 0.12

0.22 ± 0.11

0.18 ± 0.12

0.22 ± 0.12

0.16 ± 0.09

0.16 ± 0.10

Histidine

5.43 ± 0.73

6.39 ± 1.20

4.70 ± 0.34

5.33 ± 1.33

4.34 ± 0.72

5.94 ± 1.18

4.38 ± 1.28

4.02 ± 0.66*

4.74 ± 0.80

4.42 ± 0.54

4.36 ± 0.69

8.10 ± 2.69*

3Methyl histidine

0.49 ± 0.12

0.52 ± 0.12

0.46 ± 0.10

0.50 ± 0.18

0.50 ± 0.14

0.65 ± 0.24

0.48 ± 0.16

0.36 ± 0.11

0.48 ± 0.16

0.55 ± 0.11

0.35 ± 0.07

0.54 ± 0.20

Plasma branched-chain amino acid concentration increased by approximately five times in BCAARQ, BCAAR, BCAAQ, BCAAP, BCAAE, EAA groups compared with the DW group. Plasma tryptophan, histidine, tyrosine, threonine, serine and glycine concentration decreased in the groups that received solutions containing BCAA. Plasma proline concentration increased in Arg and AQ groups. Values are means ± SD

Comparisons with the DW group was conducted with a Dunnett’s test after ANOVA for multiple comparison (* P < 0.05)

Discussion

The object of this study was to investigate the effects of UV irradiation on the rate of skin tropocollagen protein synthesis and to determine which amino acid increases dermal tropocollagen protein synthesis in UV-irradiated mice. It was observed that the tropocollagen FSR generally decreased after UVB irradiation and that some amino acid mixtures, such as BCAA + Arg + Gln, BCAA + Gln, BCAA + Gln + Pro, and a mixture of essential amino acids significantly increased the tropocollagen FSR in UV-irradiated mice. This is the first paper to indicate which single amino acids or amino acid mixtures can correct UV irradiation-induced changes in collagen protein synthesis.

Decreasing amounts of collagen result in skin aging, such as formation of wrinkles and sagging skin, and the main cause of skin aging is UV irradiation (Takema et al. 1996). However, few studies have examined collagen protein metabolism. To help prevent skin aging, it is important to understand how UV irradiation induces changes in dermal collagen metabolism and how these changes can be reversed. A long-term study of changes in the amount dermal collagen is necessary because collagen protein turnover is very slow. Thus, we focused on measuring the FSR of tropocollagen, a soluble collagen that includes intracellular and extracellular procollagen. In many reports, 13C or 14C-labeled proline is used as a tracer to measure the FSR of collagen, and hydroxyproline enrichment is measured because hydroxyproline is specifically modified from the proline within collagen protein (McAnulty and Laurent 1987). However, it is thought that proline is not a suitable tracer for measuring collagen protein metabolism, especially in investigating the effect of amino acid supplementation on collagen protein metabolism because proline stimulates collagen synthesis in human fibroblast cells (Bellon et al. 1987). For this reason, we used l-[ring-2H5]-phenylalanine as a tracer and a method involving extraction of tropocollagen to measure the collagen FSR. Phenylalanine is commonly used to investigate the effects of amino acid supplementation on protein metabolism. The FSR of tropocollagen tended to decrease after one-time UV irradiation, and a similar decrease was observed after additional UV irradiation (Fig. 2). This result corresponded to that obtained by Fisher et al. (2000), who found that human skin procollagen mRNA levels decreased with UV irradiation. Thus, it was confirmed that UVB irradiation also decreases the collagen protein synthesis rate.

Several amino acids used in the present study, such as EAA, BCAA, Gln, Glu, and Arg, have been reported to stimulate protein synthesis in several tissues in in vivo and in vitro studies (Anthony et al. 2000; Bellon et al. 1987, 1995; Kimball and Jefferson 2004; Krause et al. 2002a; Oehler and Roth 2003; Proud 2004; Stechmiller et al. 2005; Stoll et al. 1992; Tipton et al. 1999; Xu et al. 2001). In particular, Arg, Gln, and their metabolites increased collagen synthesis in vitro or in wound healing in rats (Bellon et al. 1987, 1995; Shi et al. 2002, 2003; Stechmiller et al. 2005). However, there is little information on the effect of amino acid on dermal collagen protein synthesis after UV irradiation. It is important to investigate UV irradiation’s effect in mice because the process of collagen deposition differs between UV irradiation and wounds (Fisher 2005; Johnstone and Farley 2005). Some amino acid mixtures containing BCAA, such as EAA, BCAA + Arg + Gln, BCAA + Gln, and BCAA + Pro, significantly increased the FSR of tropocollagen (Fig. 3). BCAA in particular, but also leucine and its metabolites, modulate mammalian targets of rapamycin (mTOR) and stimulate phosphorylation of the 70-kDa ribosomal protein S6 kinase (p70S6K) and eukaryotic initiation factor-binding protein-1 (4E-BP1), initiating translation and transcription in protein synthesis (Anthony et al. 2000; Kimball and Jefferson 2004; Meijer 2003; Proud 2004; Xu et al. 2001). However, BCAA and BCAA + Glu did not increase the FSR of dermal tropocollagen (Fig. 3). In addition, other amino acids, such as Arg, Gln, Pro, Arg + Gln, also did not increase the FSR (Fig. 3). This result indicates that while BCAA is important for skin tropocollagen synthesis, other specific amino acids, such as Gln or Pro, are also necessary to stimulate dermal tropocollagen synthesis.

In an in vitro study, Bellon and Karna showed that Gln and its metabolites (glutamate, pyrroline-5-carboxylate, arginine) increase collagen synthesis and suggested that de novo synthesized proline is important for collagen synthesis (Bellon et al. 1995, 1987; Karna et al. 2001). In the present study, the FSR of tropocollagen did not increase when amino acids containing precursors of proline (Gln, Arg, BCAA + Glu and Arg + Gln) were administered, but did increase with an amino acid mixture containing exogenous proline (BCAA + Pro). In addition, plasma proline concentrations were not increased by collagen synthesis-stimulating amino acid mixtures containing proline precursors (BCAA + Gln, BCAA + Gln + Arg), but were slightly increased by Arg + Gln and Arg, neither of which stimulated the tropocollagen FSR. These results indicate that de novo proline synthesis is not the main cause of increased collagen protein synthesis. Proline constitutes one-third of collagen protein’s amino acid residues. However, there is little information proline supplementation’s effect on dermal skin collagen synthesis. Further study is needed to understand the mechanism underlying the effect of BCAA + Pro on the FSR of tropocollagen.

Xu found that the combination of leucine and glutamine synergistically stimulates the activity of S6K in pancreatic beta cells. Some reports indicate that glutamine regulates protein synthesis (Xu et al. 2001). For example, glutamine restores energy metabolism into cells (Krause et al. 2002b), increases cell swelling (Oehler and Roth 2003), and activates GAPP (glutamate dependent protein phosphatase, which correlates with mTOR activation) (Krause et al. 2002a; Stoll et al. 1992). Arginine also improves wound healing by increasing collagen synthesis; the mechanism of this effect is thought to be the stimulation of growth hormone secretion and nitric oxide synthesis (Stechmiller et al. 2005). Williams reported that an orally administered amino acid mixture consisting of metabolites of leucine (b-hydroxy-b-methylbutyrate), arginine, and glutamine increased the collagen content in subcutaneously implanted tubes in healthy volunteers (Williams et al. 2002). In addition, Corsetti reported that amino acid mixtures that included leucine, proline, lysine, and glycine improved wound healing associated with the modulation of nitric oxidate synthase and transforming growth factor-β1 (Corsetti et al. 2010). Dioguardi (2008) also reported that collagen synthesis is efficiently maintained only when specific amino acids are continuously available and present in a specific ratio. Therefore, a possible explanation of our findings is that BCAA + Gln and BCAA + Gln + Arg synergistically stimulate dermal tropocollagen protein synthesis using each amino acid’s individual effects on protein synthesis. In addition, insulin is a powerful protein synthesis stimulator, and leucine and arginine stimulate insulin secretion. However, insulin was not the main cause of the increase of the dermal tropocollagen FSR by the amino acid mixtures, because there was no correlation between insulin and the tropocollagen FSR in any group (r 2  = 0.034; Fig. 6). EAA is known to increase the FSR of skeletal muscle protein (Tipton et al. 1999). In the present study, EAA was the only amino acid observed to increase the FSR of skeletal muscle protein (data not shown). Thus, the tropocollagen FSR improvement resulting from EAA is associated with the improvement of whole-body protein metabolism.

In conclusion, UVB irradiation decreased the FSR of skin tropocollagen, while BCAA + Arg + Gln, BCAA + Gln, BCAA + Pro, and EAA increased the FSR of skin tropocollagen independently of insulin. However, single amino acids and BCAA did not increase the FSR. It should be noted that combinations of specific amino acids, especially BCAA + Gln or BCAA + Pro are vital in stimulating the FSR of skin tropocollagen independently of insulin. However, the dermal collagen protein synthesis stimulation mechanism of these amino acids mixtures is unclear. Further study is necessary to understand the mechanism of the increase tropocollagen FSR by these amino acids.

Notes

Acknowledgments

We thank Takashi Suzuki, Sayo Inoue, and Shinobu Tanimoto for their assistance with the experimental trial.

Conflict of interest

The authors declare that they have no conflict of interest.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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Copyright information

© The Author(s) 2011

Authors and Affiliations

  • Hitoshi Murakami
    • 1
    Email author
  • Kazutaka Shimbo
    • 1
  • Yoshiko Inoue
    • 1
  • Yoshinobu Takino
    • 2
  • Hisamine Kobayashi
    • 1
  1. 1.Frontier Research Laboratories, Institute for InnovationAjinomoto Co., IncKawasakiJapan
  2. 2.Research Institute for Bioscience Products and Fine ChemicalsAjinomoto Co., IncKawasakiJapan

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