Dietary supplementation with betaine or glycine improves the carcass trait, meat quality and lipid metabolism of finishing mini-pigs

Abstract

The objective of the study is to evaluate and compare the effects of betaine or glycine on carcass trait, meat quality and lipid metabolism of finishing Huan Jiang mini-pigs. Betaine called trimethylglycine is a methyl derivative of glycine, but few researches were conducted to compare the impact of dietary betaine and glycine on pigs. One hundred and forty-four Huan Jiang mini-pigs (body weight = 10.55 ± 0.15 kg; 70 d) were randomly divided to 3 treatment groups (basal diet, glycine or betaine). Results indicated that dietary betaine increased the average daily gain (ADG) and final weight (P < 0.05). Dietary glycine or betaine markedly reduced average backfat thickness (P < 0.05) and heightened lean percentage (P < 0.01) compared to the control group. Moreover, in comparison with the control group, betaine significantly improved the redness (a∗) and tenderness (shear force) of the longissimus dorsi (LD) muscle (P < 0.05), whereas glycine only raised the value of a∗ of the LD muscle (P < 0.05). These results showed that diet supplemented with 0.25% betaine and equimolar amounts of glycine could regulate cascass trait and meat quality of finishing Huan Jiang mini-pigs, and the effect of betaine was superior to that of glycine.

1. Introduction

Betaine, i.e., N,N,N-trimethylglycine, is a methyl derivative of glycine and a coproduct of extracting molasses from sugar beet (Cholewa et al., 2014). It is generally found in animals and plants and is a secondary metabolite of choline oxidative decomposition (Eklund et al., 2005). Betaine has many functions, mainly as a methyl donor involved in methionine-homocysteine cycle and as a penetrant to maintain body osmotic pressure balance (Martins et al., 2012; Albuquerque et al., 2017). Several researchers report that 0.25% betaine is moderate to increase lean percentage and reduce average backfat thickness and fat percentage in finishing pigs (Matthews et al., 2001; Siljander-Rasi et al., 2016; Li et al., 2017a). A previous study suggests that diet supplemented with betaine increases final weight and average daily gain (ADG) (Huang et al., 2006), although no difference is observed in other studies (Matthews et al., 2001; Martins et al., 2012). Another research shows that the average backfat thickness is lower in finishing pigs fed with betaine than that in the control group (Yu et al., 2004), but others indicate no effect noticed (Fernández-Fígares et al., 2008; Martins et al., 2012). In addition, some reports show that betaine increases lean percentage (Matthews et al., 2001; Huang et al., 2007), whereas others indicates that betaine has no effect on lean percentage (Rojas-Cano et al., 2011). It is also reported that intramuscular fat (IMF) increases in finishing pigs fed with betaine (Martins et al., 2012), but no significant difference is observed in the study of Rojas-Cano et al. (2011). These inconsistent results suggested that impact of betaine on growth performance and meat quality in finishing pigs is still ambiguous and needs further research.

Betaine is a methyl derivative of glycine. Glycine can improve muscle cell growth by enhancing protein synthesis and inhibiting protein degradation in C2C12 myoblasts (Sun et al., 2016). Some researches indicate that glycine enhances muscle protein mass as a functional amino acid in piglets (Wang et al., 2014; Liu et al., 2016b). However, there are few studies on the influence of glycine in finishing pigs. We consider whether glycine possesses a similar function to betaine in affecting carcass trait, meat quality and lipid metabolism in finishing pigs. Therefore, equimolar glycine and betaine are supplemented in the present experimental diets and compare the difference.

The Huan Jiang mini-pig is an indigenous pig breed in South China, with soft black skin and delicious meat, which is very popular in the local area. Due to its typical obese genotype, more and more attention is being paid to lipid metabolism research. Moreover, its physiological and anatomical structure is similar to human beings (Liu et al., 2015). Thus, Huan Jiang mini-pig was selected as an animal model in the present experiment.

2. Materials and methods

2.1. Animals and experiments

All of the experimental protocols were carried out in compliance with procedures approved by the Animal Ethics Committee of South China Agricultural University. A total of 144 Huan Jiang mini-pigs (neutered boars) with an average initial body weight of 10.55 ± 0.15 kg (mean ± SEM) were assigned to 3 treatment groups with a completely randomized design, with 8 replications of 6 pigs per replicate (pen). The treatment diets included a corn-soybean meal basal diet, which was supplemented with 0.25% betaine, and an equimolar amount of glycine (0.16%; Table 1). In addition, betaine was added in the form of betaine hydrochloride (0.35%, Shandong Xiangweisi Biotechnology Co., Ltd.). The basal diet was formulated to meet the nutritional requirement of finishing pigs according to Chinese National Feeding Standard for Swine (2004). All of the pigs were housed in pens of 2.0 m × 3.0 m with a concrete slotted floor with an area of 1.0 m × 3.0 m and had free access to water and diets throughout the whole experiment. The experimental period lasted for 60 d following a 3-d preliminary feeding period supplemented with the same basic diet.

Table 1.

Ingredients and nutrient levels of experimental diets (as-fed basis).¹

Item	Control	Glycine	Betaine
Ingredients, %
Corn	65.00	65.20	64.71
Soybean meal	19.40	19.00	19.50
Wheat bran	12.46	12.50	12.30
Lysine	0.14	0.14	0.14
CaHPO4	0.75	0.75	0.75
Limestone	0.95	0.95	0.95
Salt	0.30	0.30	0.30
Premix2	1.00	1.00	1.00
Betaine NaCl	0.00	0.00	0.35
Glycine	0.00	0.16	0.00
Nutrient, %
Digestible energy, MJ/kg	13.62	13.59	13.58
Crude protein3	15.07	15.08	15.06
Lys	0.75	0.74	0.75
Met + Cys	0.50	0.50	0.50
Thr	0.47	0.47	0.47
Ca	0.63	0.63	0.63
Total P	0.53	0.53	0.53
Available P	0.24	0.24	0.24

¹Basal diet formulated according to the Chinese National Feeding Standard for Swine.

²Provided per kilogram of diet: Fe, 400 mg as FeSO₄·7H₂O; Cu, 19.8 mg as CuSO₄·₅H₂O; I, 0.20 mg as KI; Se, 0.56 mg as NaSeO₃; Zn, 359 mg as ZnSO₄·₇H₂O; Mn, 10.2 mg as MnSO₄·H₂O; 5 mg vitamin K; 2 mg vitamin B₁; 15 mg vitamin B₂; 30 μg vitamin B₁₂; 5,400 IU vitamin A; 110 IU vitamin D₃; 18 IU vitamin E; 20 mg antioxidants.

³Measured nutrient levels (DM basis).

2.2. Samples collection

At the end of the trial, all the pigs were fasted overnight (12 h), and one pig of each replicate with the average final body weight was selected (8 pigs of each group) to slaughter by electrical stunning and bleeding in a commercial abattoir. Before slaughter, blood samples were collected into 10-mL anticoagulant centrifuge tubes and placed at room temperature for 2 h, then centrifuged at 3,000 × g for 10 min at 4 °C. Serum was collected and stored at −80 °C until further analysis. The longissimus dorsi (LD) muscle between the 6th and 7th ribs was immediately excised and stored at −20 °C for determination of the chemical composition, or placed in liquid N₂ and then stored at −80 °C for the analysis of quantitative real-time PCR.

2.3. Carcass trait analysis

The left side of the carcass was weighed and then split up into skeletal muscle and fat as previously described (Martins et al., 2012). Loin-eye area and average backfat thickness (3rd to 4th lumbar vertebra, 10th to 11th, and the last rib) were measured.

2.4. Meat quality assessment

The pH value, color, shear force, water-holding capacity, cooking loss and IMF content of the LD muscle were measured to evaluate pork quality. A hand-held pH meter (pH-STAR, SFK-Technology, Denmark) was used to determine the pH values at 45 min and 24 h postmortem. The LD muscle was given 10 to 15 min for the color to develop after cutting. Subsequently, meat color including lightness (L∗), redness (a∗) and yellowness (b∗) was measured using a hand-held colorimeter (CR-410, Minolta Camera, Co., Osaka, Japan). Water-holding capacity, cooking loss and shear force were determined as described in our previous study (Li et al., 2018). Shear force was measured using a texture analyzer (TA-tx2i Texture Analyzer, Stable Micro Systems, Godalming, UK) equipped with a Warner–Bratzler shear force device using cooked and cooled samples.

2.5. Serum biochemical indexes measurements

Alanine aminotransferase, aspartate aminotransferase), total protein, albumin, urea nitrogen, creatinine, blood ammonia in serum were measured with automatic biochemical analyzer (Beckman CX4; Beckman Coulter, Germany) and commercial kits (Leadman Biotech Limited, Beijing, China) as specified by the manufacturer.

2.6. Measurement of free amino acids in serum and LD muscle

The free amino acid profile in serum was measured as previously described (Hu et al., 2019). Firstly, 1 mL of 8% 5-sulfosalicylic acid was added to tube including 1 mL of serum, mixed, stood for 15 min, and then centrifuged at 9,390 × g at room temperature for 10 min. Subsequently, 0.22 μm membrane was used to filter the supernatant before measurement. The free amino acid concentrations in LD muscle were determined as our previous studies outlined (Duan et al., 2016b; Liu et al., 2016a). Approximately 0.5 g of freeze-dried muscle sample was homogenized in 10 mL of 0.01 mol/L hydrochloric acid and shaken for 30 min. Then the solution added up to 25 mL with 0.01 mol/L hydrochloric acid. After centrifuging at 13,520 × g at room temperature for 10 min, 1 mL of the supernatant was mixed with 1 mL of 8% 5-sulfosalicylic acid and centrifuged again. One milliliter of the supernatant was chosen to filter with 0.22 μm membrane before analysis. All samples were determined by an ion-exchange AA analyzer (L8800, Hitachi, Tokyo, Japan).

2.7. Measurement of fatty acid composition and IMF in LD muscle

The IMF content was measured using the Soxhlet extraction method as previously outlined (Duan et al., 2016a). The free fatty acid concentrations were measured as described in detail (Li et al., 2017a). The fatty acid composition of LD muscle was measured as previously described (Li et al., 2015). Lipids were extracted from the LD muscle samples by the benzene-petroleum ether (1:1, vol/vol) procedure. Fatty acid methyl esters were prepared using 0.4 mol/L KOH/methanol solution, then determined by an Agilent 6890N gas chromatographer equipped with a flame ionization detector (Agilent Technologies) and A CP-Sil 88 fused silica open tubular capillary column (100 m × 0.25 nm; Chrompack). The method of gas chromatography analysis was as follows: original temperature was set at 45 °C for 4 min, raised to 175 °C at 13 °C/min, held at 175 °C for 27 min, warmed from 175 to 215 °C at 4 °C/min, and then held at 215 °C for 35 min. The injector and detector temperatures were stabilized at 250 °C. The carrier gas was hydrogen and the flow rate was set at 30 mL/min. The concentration of individual fatty acids was quantified by the precise standard and expressed as a percentage of the total fatty acids.

2.8. Quantitative real-time PCR analysis

The quantitative real-time PCR was conducted as described in our previous study (Zhong et al., 2019). The TRIzol reagent (Invitrogen, Carlsbad, CA, USA) was used to isolate RNA from LD muscle tissues (Invitrogen, Carlsbad, CA, US) following the manufacturer's protocol. Quantitative real-time PCR was performed with an ABI 7900HT Real-time PCR system (Applied Biosystems, Branchburg, NJ) to determine relative mRNA expression levels of the selected genes.

Primers of the target genes were designed using Primer 5.0 software (Table 2). To normalize the mRNA expression levels of target genes, the housekeeping gene glyceraldehyde-3-phosphate dehydrogenase (GAPDH) was selected as an internal control. The procedures of quantitative real-time PCR were set as follows: incubated at 95 °C for 10 min, denatured at 95 °C for 15 s with 40 cycles, annealed at 60 °C for 60 s, and extended at 72 °C for 30 s. The mRNA expression levels of target genes in arbitrary unit were acquired from the value of the threshold cycle (C_t) of the real-time PCR as related to that of internal control using the comparative 2^−ΔΔCt method (Duan et al., 2019).

Table 2.

Primers used for quantitative real-time PCR.

Genes	Primers	Sequences (5′ to 3′)	Product size, bp
ACC	Forward	TTCCAGGCACAGTCCTTAGG	161
	Reverse	TCATCCAACACGAGCTCAGT
FAS	Forward	CTACCTTGTGGATCACTGCATAGA	114
	Reverse	GGCGTCTCCTCCAAGTTCTG
CPT1B	Forward	ATGGTGGGCGACTAACT	321
	Reverse	TGCCTGCTGTCTGTGAG
HSL	Forward	GCAGCATCTTCTTCCGCACA	195
	Reverse	AGCCCTTGCGTAGAGTGACA
FAT/CD36	Forward	CTGGTGCTGTCATTGGAGCAGT	160
	Reverse	CTGTCTGTAAACTTCCGTGCCTGTT
FATP1	Forward	GGAGTAGAGGGCAAAGCAGG	208
	Reverse	AGGTCTGGCGTGGGTCAAAG
PPARγ	Forward	AGGGCCAAGGATTCATGACA	248
	Reverse	GTGGTTCAACTTGAGCTGCA
SREBP1c	Forward	GCGACGGTGCCTCTGGTAGT	218
	Reverse	CGCAAGACGGCGGATTTA
MyHC I	Forward	GGCCCCTTCCAGCTTGA	63
	Reverse	TGGCTGCGCCTTGGTTT
MyHC IIa	Forward	TTAAAAAGCTCCAAGAACTGTTTCA	100
	Reverse	CCATTTCCTGGTCGGAACTC
MyHC IIx	Forward	AGCTTCAAGTTCTGCCCCACT	76
	Reverse	GGCTGCGGGTTATTGATGG
MyHC IIb	Forward	CACTTTAAGTAGTTGTCTGCCTTGAG	80
	Reverse	GGCAGCAGGGCACTAGATGT
GAPDH	Forward	AAGGAGTAAGAGCCCCTGGA	140
	Reverse	TCTGGGATGGAAACTGGAA

ACC = acetyl-CoA carboxylase α; FAS = fatty acid synthase; CPT1B = carnitine palmitoyl transferase 1B; HSL = hormone-sensitive lipase; FAT/CD36 = fatty acid translocase; FATP1 = fatty acid transport protein 1; PPARγ = peroxisome proliferator-activated receptor γ; SREBP1c = sterol regulatory element binding protein-1c; MyHC = myosin heavy chain; GAPDH = Glyceraldehyde-3-phosphate dehydrogenase.

2.9. Statistical analysis

To assess influence of treatments, all data in the current study was analyzed by one-way analysis of variance (ANOVA) using the SAS 8.2 software (Cary, NC, USA) followed by Duncan's multiple comparison test. Means and standard error of mean (SEM) were adopted to express results. P < 0.05 was considered statistically significant and 0.05 < P < 0.10 was considered a trend toward significance.

3. Results

3.1. Growth performance

As shown in Table 3, final weight (P = 0.08) and ADG (P = 0.06) of the pigs fed with 0.25% betaine were higher than those of control group, but no difference was observed between the glycine and the control groups. In addition, no significant difference was noticed in the average daily feed intake (ADFI) and the ratio of feed intake to body weight gain (Feed:Gain) among the 3 treatment groups (P > 0.05).

Table 3.

Impact of diet supplemented with betaine or glycine on growth performance of finishing Huan Jiang mini-pigs.

Item	Control	Glycine	Betaine	SEM	P-value
Initial weight, kg	10.59	10.55	10.53	0.15	0.97
Final weight, kg	30.21b	31.39ab	32.29a	0.32	0.08
ADG, g/d	326.90b	347.02ab	360.49a	1.24	0.06
ADFI, g/d	972.35	999.74	979.35	3.12	0.74
Feed:Gain ratio1	2.98	2.89	2.80	0.17	0.26

ADG = average daily gain; ADFI = average daily feed intake.

^{a, b} Within a row, values with different superscripts differ significantly at P < 0.05 and a trend toward significance at P < 0.10. Data are expressed as means ± SEM, n = 8.

¹Feed:Gain ratio = the ratio of feed intake to body weight gain.

3.2. Carcass trait and meat quality

Betaine and glycine both decreased the average backfat thickness (P < 0.05) and increased lean percentage (P < 0.01) when compared to the control group. The 45 min pH value, 24 h pH value, L∗ value, b∗ value, water-holding capacity, and cooking loss had no significant difference among the 3 treatment groups (P > 0.05). Nevertheless, a∗ value was higher in the betaine and the glycine groups than the control group (P = 0.04). Moreover, the shear force showed a notable decrease in the betaine group compared to the other 2 groups (P = 0.01; Table 4).

Table 4.

Impact of diet supplemented with betaine or glycine on carcass trait and meat quality of finishing Huan Jiang mini-pigs.

Item	Control	Glycine	Betaine	SEM	P-value
Average backfat thickness, mm	19.64a	18.00b	18.09b	0.40	0.05
Loin eye area, mm2	893.60	931.81	897.70	3.65	0.78
Lean percentage, %	38.11b	40.69a	40.87a	0.41	<0.01
pH45 min	6.29	6.31	6.39	0.17	0.73
pH24 h	5.46	5.48	5.34	0.12	0.13
L∗ (lightness)	45.16	44.57	45.14	0.44	0.76
a∗ (redness)	15.77b	16.71a	16.78a	0.30	0.04
b∗ (yellowness)	4.71	4.35	4.42	0.20	0.12
Water-holding capacity, %	20.24	19.68	18.41	0.68	0.67
Cooking loss, %	58.34	56.93	56.73	0.43	0.12
Shear force, N	46.77a	45.08a	39.37b	0.74	0.01

^a,b Within a row, values with different superscripts differ significantly at P < 0.05 and a trend toward significance at P < 0.10. Data are expressed as means ± SEM, n = 8.

3.3. Serum biochemical indexes

The concentrations of serum metabolites with different dietary treatments are presented in Table 5. Diet supplemented with betaine or glycine did not affect the concentrations of alanine aminotransferase, aspartate aminotransferase, total protein, albumin, urea nitrogen, creatinine, and blood ammonia in serum of the pigs (P > 0.05).

Table 5.

Impact of diet supplemented with betaine or glycine on serum metabolites of finishing Huan Jiang mini-pigs.

Item	Control	Glycine	Betaine	SEM	P-value
ALT, U/L	62.67	63.69	68.61	0.89	0.22
AST, U/L	62.10	65.00	65.00	1.08	0.81
TP, g/L	74.55	74.66	74.97	0.50	0.93
ALB, g/L	49.21	48.34	47.64	0.44	0.21
NH3, μmol/L	206.72	207.08	210.52	1.24	0.84
BUN, mmol/L	4.43	4.77	4.98	0.24	0.13
CREA, μmol/L	69.00	70.60	73.00	0.70	0.21

ALT = alanine aminotransferase; AST = aspartate aminotransferase; TP = total protein; ALB = albumin; NH₃ = ammonia; BUN = urea nitrogen; CREA = creatinine.

Data are expressed as means ± SEM, n = 8.

3.4. Free amino acid profiles in serum and skeletal muscle

As can be seen from Table 6, the concentration of essential amino acids in serum did not change significantly (P > 0.05). An obvious increase was observed in glycine concentration in the glycine group compared to the other 2 groups (P < 0.05). Moreover, the cysteine concentration in the pigs fed with glycine or betaine was lower than the control group (P < 0.01).

Table 6.

Impact of dietary betaine on serum free amino acids of finishing Huan Jiang mini-pigs (μg/mL).

Item	Control	Glycine	Betaine	SEM	P-value
EAA
Lysine	22.37	22.84	22.83	0.34	0.59
Methionine	4.14	4.21	4.27	0.18	0.69
Valine	33.55	33.95	33.62	0.59	0.96
Isoleucine	15.63	15.95	15.02	0.38	0.37
Leucine	25.03	24.93	25.08	0.49	0.99
Phenylalanine	12.90	12.35	13.00	0.27	0.12
Histidine	13.25	13.40	13.48	0.44	0.96
Threonine	17.92	17.92	17.97	0.46	1.00
NEAA
Alanine	26.05	26.24	24.87	0.54	0.53
Aspartic acid	3.04	3.23	3.15	0.18	0.42
Glutamic acid	34.44	34.35	35.14	0.71	0.93
Arginine	33.35	33.48	33.07	0.53	0.95
Glycine	40.11b	46.49a	41.37b	0.64	<0.01
Serine	8.32	8.63	8.90	0.30	0.39
Tyrosine	11.51	11.27	11.72	0.34	0.68
Cysteine	5.72a	4.37b	4.18b	0.30	<0.01
Proline	17.27	17.63	17.58	0.35	0.78
Total EAA	144.78	145.56	145.27	0.80	0.96
Total NEAA	179.82	185.69	179.98	0.83	0.11
Total AA	324.60	331.25	325.25	0.92	0.18

EAA = essential amino acids; NEAA = non-essential amino acids.

^a,b Within a row, values with different superscripts differ significantly at P < 0.05 and a trend toward significance at P < 0.10. Data are expressed as means ± SEM, n = 8.

The free amino acid profiles in LD muscle are presented in Table 7. A significant increase was noticed in methionine and threonine concentrations in the glycine group and the betaine group (P < 0.01). Serine concentration showed an increasing trend in the glycine and the betaine group compared to the control group (P < 0.10). In addition, the cysteine concentration in the control group was higher than the other 2 groups (P < 0.01). The essential amino acids (EAA), non-essential amino acids (NEAA) and total amino acids (TAA) did not change among the 3 treatment groups (P > 0.05).

Table 7.

Impact of diet supplemented with betaine on free amino acids of longissimus dorsi muscle in finishing Huan Jiang mini-pigs (μg/g).

Item	Control	Glycine	Betaine	SEM	P-value
EAA
Lysine	81.64	86.17	82.82	1.01	0.59
Methionine	59.05b	63.03a	63.88a	0.58	<0.01
Valine	111.79	104.28	98.02	1.23	0.14
Isoleucine	90.14	87.93	87.25	0.94	0.75
Leucine	129.57	124.85	119.14	1.25	0.34
Phenylalanine	93.57	92.81	94.65	0.70	0.70
Histidine	62.01	64.35	62.10	0.84	0.70
Threonine	71.09b	84.28a	81.46a	0.96	<0.01
NEAA
Alanine	437.75	494.87	488.10	2.63	0.15
Aspartic acid	250.48	261.96	274.28	2.04	0.45
Glutamic acid	201.78	196.43	198.52	1.56	0.89
Arginine	58.51	59.20	57.03	0.70	0.61
Glycine	281.43	317.01	292.62	2.65	0.52
Serine	62.38	70.59	70.39	0.97	0.10
Tyrosine	83.91	74.98	79.93	0.96	0.12
Cysteine	21.63a	18.55b	18.17b	0.48	<0.01
Proline	113.85	116.51	113.53	0.92	0.69
Total EAA	698.86	707.73	689.33	2.10	0.65
Total NEAA	1,511.72	1,610.10	1,592.55	3.83	0.29
Total AA	2,210.58	2,317.83	2,281.88	4.08	0.35

EAA = essential amino acids; NEAA = non-essential amino acids.

^a,b Within a row, values with different superscripts differ significantly at P < 0.05 and a trend toward significance at P < 0.10. Data are expressed as means ± SEM, n = 8.

3.5. Fatty acid profile in skeletal muscle

The free fatty acid (FFA) and IMF content in the glycine and the betaine groups were lower than that of the control group (P < 0.01). Diet supplemented with betaine and glycine greatly altered the fatty acid composition of LD muscle (Table 8). Betaine and glycine decreased the concentration of saturated fatty acid (SFA, P < 0.05), whereas the concentration of polyunsaturated fatty acid (PUFA) and PUFA-to-SFA ratio markedly increased relative to the control group (P < 0.01). The concentrations of C18:3n3 and C20:4n6 were higher in the glycine and betaine groups when compared to the control group (P < 0.01). Furthermore, diet supplemented with glycine and betaine did not affect the value of monounsaturated fatty acid (MUFA, P > 0.05).

Table 8.

Impact of diet supplemented with betaine on fatty acid composition and intramuscular fat content of longissimus dorsi muscle in finishing Huan Jiang mini-pigs (% of total fatty acids).

Item	Control	Glycine	Betaine	SEM	P-value
FFA, mmol/g protein	0.43a	0.23b	0.23b	0.10	<0.01
IMF, %	4.45a	3.91b	3.99b	0.19	<0.01
C14:0	1.19a	0.87b	0.93b	0.12	<0.01
C14:1	0.05b	0.05a	0.05b	0.03	0.04
C15:0	0.09	0.09	0.10	0.04	0.55
C16:0	24.44	22.94	23.17	0.35	0.02
C16:1	3.26	2.90	2.86	0.22	0.16
C17:0	0.84	0.74	0.82	0.12	0.27
C18:0	12.85	12.95	13.13	0.27	0.68
C18:1n9t	0.13a	0.12b	0.12b	0.03	<0.01
C18:1n9c	32.21	31.53	32.00	0.41	0.66
C18:2n6c	15.98b	17.02a	16.58ab	0.32	0.10
C20:0	0.22a	0.18b	0.19ab	0.06	0.02
C18:3n6	0.15	0.16	0.16	0.05	0.38
C20:1	0.75	0.70	0.75	0.08	0.16
C18:3n3	0.30b	0.33a	0.33a	0.05	0.05
C20:2	0.40	0.44	0.43	0.08	0.43
C20:3n6	0.63	0.65	0.65	0.07	0.59
C20:4n6	6.00b	7.43a	7.14a	0.27	<0.05
C20:5n3	0.23	0.20	0.21	0.07	0.27
C22:6n3	0.23	0.25	0.23	0.08	0.75
SFA1	39.63a	37.77b	38.33b	0.37	0.01
MUFA2	36.41	35.31	35.77	0.43	0.43
PUFA3	23.93b	26.48a	25.73a	0.39	<0.01
PUFA:SFA ratio	0.61b	0.70a	0.67a	0.07	<0.01

FFA = free fatty acid; IMF = intramuscular fat; SFA = saturated fatty acid; MUFA = monounsaturated fatty acid; PUFA = polyunsaturated fatty acid.

^a,b Within a row, values with different superscripts differ significantly at P < 0.05 and a trend toward significance at P < 0.10. Data are expressed as means ± SEM, n = 8.

¹SFA = C14:0 + C15:0 + C16:0 + C17:0 + C18:0 + C20:0.

²MUFA = C14:1 + C16:1 + C18:1n9t + C18:1n9c + C20:1.

³PUFA = C18:2n6c + C18:3n6 + C18:3n3 + C20:2 + C20:3n6 + C20:4n6 + C20:5n3 + C22:6n3.

3.6. The relative mRNA expression levels of myosin heavy chain (MyHC) and the genes related to lipid metabolism

The gene expression level of MyHC I was markedly up-regulated in LD muscle in the betaine group (P < 0.05, Fig. 1A). However, there was no pronounced difference in the mRNA expression levels of MyHC IIa, MyHC IIb, and MyHC IIx among the 3 dietary groups (P > 0.05).

Fig. 1.

Betaine promoted the synthesis of type I muscle fibers in longissimus dorsi muscle; betaine (Bet) and glycine (Gly) inhibited fat synthesis and promoted fat catabolism in longissimus dorsi muscle. (A) The relative mRNA expression levels of the key genes related to skeletal muscle fiber type including myosin heavy chain (MyHC) I, MyHC IIa, MyHC IIb, and MyHC IIx (n = 8). (B) The relative mRNA expression levels of the key genes related to lipid metabolism including fatty acid transport protein 1 (FATP1), fatty acid translocase (FAT/CD36), acetyl-CoA carboxylase α (ACC), fatty acid synthase (FAS), hormone-sensitive lipase (HSL), carnitine palmitoyl transferase 1B (CPT1B), sterol regulatory element binding protein-1c (SREBP1c), and peroxisome proliferator-activated receptor γ (PPARγ) (n = 8). ^{a, b} Bars with different letters differ significantly at P < 0.05 and a trend toward significance at P < 0.10. Data are expressed as means ± SEM.

The mRNA expression levels of the genes involved in muscle lipid metabolism: Lipid intake includes fatty acid translocase (FAT/CD36) and fatty acid transport protein 1 (FATP1), lipogenesis includes acetyl-CoA carboxylase α (ACC) and fatty acid synthase (FAS), lipolysis includes hormone-sensitive lipase (HSL) and fatty acid oxidation includes carnitine palmitoyl transferase 1B (CPT1B), and transcription factors includes sterol regulatory element binding protein-1c (SREBP1c) and peroxisome proliferator-activated receptor γ (PPARγ). As shown in Fig. 1B, in comparison with the control group, betaine lowered the relative mRNA expression levels of FATP1 and SREBP1c, whereas no significant differences were observed in the value of FAT/CD36 in the present study (P > 0.05). Additionally, betaine and glycine both down-regulated the mRNA expression levels of ACC, FAS, and PPARγ (P < 0.05), and the value of HSL and CPT1B were up-regulated (P < 0.05).

4. Discussion

The present study was designed to investigate and compare the effects of betaine or glycine on carcass trait, meat quality and lipid metabolism in finishing Huang Jiang mini-pigs. Our results indicated that betaine increased final weight and ADG, but had no impact on ADFI and Feed:Gain ratio. The addition of glycine did not improve the growth performance parameters of the pigs. Additionally, betaine or glycine both decreased average backfat thickness and betaine also increased lean percentage. It was consistent with previous studies (Matthews et al., 2001; Huang et al., 2007). The reason might be that betaine increased the synthesis of proteins and the rate of cell proliferation by regulating the response of various cells to hypertonicity (Petronini et al., 1992), or increased sarcoplasmic osmolality to increase muscle mass (Courtenay et al., 2000). Glycine also increased lean percentage, probably because it enhanced the amino acid metabolism cycle, which promoted protein synthesis of skeletal muscle (Wang et al., 2014; Liu et al., 2016b; Sun et al., 2016).

As mentioned earlier, people are keen on high-quality meat, especially excellent tenderness and juiciness (Mehta et al., 2013). Some experiments were conducted to evaluate effect of betaine on pork quality (Overland et al., 1999; Matthews et al., 2001; Martins et al., 2012), whereas the results were not consistent. It is reported that betaine does not influence L∗, a∗ and b∗ values of pork (Martins et al., 2012; Matthews et al., 2001). In our study, a∗ value of the betaine group was markedly increased in LD muscle. The reason for the discrepancy might be that the amount of dietary betaine addition was different. Furthermore, glycine also increased a∗ value of the LD muscle in the present experiment. Another finding of our study was that the dietary betaine supplementation decreased shear force, and thus improved pork tenderness. The reduction in shear force value might be related to the increase in protein content (Hwang et al., 2010). However, no changes were observed in serum metabolites of the pigs fed with betaine or glycine. The latest study indicates that specific amino acids could enhance protein synthesis and promote skeletal muscle growth through activating the key signaling pathway (Cholewa et al., 2014; Hu et al., 2019). In the present experiment, betaine or glycine partly changed the free amino acid profiles in serum and LD muscle. The content of free cysteine in serum and LD muscle was observed a reduction in the betaine and glycine groups, and free methionine in LD muscle was increased in the betaine group compared to the control group. Homocysteine is an intermediate in the synthesis of methionine and cysteine (Ganguly and Alam, 2015). Betaine participates in the methionine-homocysteine cycle, and as a methyl donor to promote homocysteine re-methylation to methionine (Schwab et al., 2006; Cholewa et al., 2014). This explained the increase of free methionine and the decrease of free cysteine. Additionally, betaine and glycine both boosted the concentration of threonine in LD muscle. A previous study indicates that threonine is converted to glycine by threonine aldolase (Joshi et al., 2010). When there is enough glycine in the body, threonine aldolase activity is inhibited, and the threonine concentration is increased. Interestingly, dietary glycine supplementation increased the content of serum glycine, but betaine had no effect. It is suggested that their physiological functions are different. Betaine is mainly involved in methyl metabolism, and glycine is primarily participated in protein synthesis in the body (Martins et al., 2012; Wang et al., 2014; Liu et al., 2016b; Sun et al., 2016).

Meat quality, especially tenderness, is extremely associated with muscle fiber type composition (Ryu and Kim, 2005; Maltin et al., 2007). According to the major subtype of MyHC in adult mammalian skeletal muscles, muscle fibers are divided into 4 types, namely type I, type IIa, type IIx, and type IIb, which influence many aspects of meat quality (Ali et al., 2008; Choi and Kim, 2009; Joo et al., 2013). In the present study, the relative mRNA expression level of MyHC I in LD muscle was higher in the betaine group than the other 2 groups. The results suggested that betaine could induce the conversion of type II fibers into type I fibers, thus improve muscle type composition. It has been pointed out that type I fiber is related to meat tenderness (Maltin et al., 2010; Lee et al., 2010), and this could explain that betaine reduced shear forces of the finishing mini-pigs in our study. Additionally, MyHC I fiber contains more myoglobin and thus improves meat color (Joo et al., 2013), which also could explain the increase in a∗ value of the pork in the present experiment.

It is indicated that IMF content is directly correlative with meat quality, particularly juiciness and flavor (Jeremiah et al., 2003; Wood et al., 2008; Hocquette et al., 2009; Li et al., 2017b). Previous studies reported that betaine could increase IMF content (Martins et al., 2012; Madeira et al., 2016; Albuquerque et al., 2017), but others pointed out no effect was obtained (Rojas-Cano et al., 2011). In the current trial, IMF content of the betaine and the glycine groups was reduced but remained at a fairly high level (Wood et al., 2008). This result might be associated with fatty acid metabolism in skeletal muscle. The available evidence indicates that FFA composition plays a quite momentous role in flavor generation and nutritional value (Wood et al., 2003). Fatty acid saturation could affect fat hardness, which in turn affects meat quality (Perry et al., 1998). An earlier research reported that the intake of a lower level of SFA with an increased ratio of PUFA to SFA could reduce the risk of coronary heart disease (Hu et al., 1999). It can be seen from the current study that betaine and glycine decreased the percentage of SFA, and at the same time increased the content of PUFA and the ratio of PUFA to SFA.

As mentioned above, the IMF content was decreased in the betaine and glycine groups. Whether the decrease related to the expression levels of the genes involved in lipid metabolism remains to be learned. Lipid uptake is mainly regulated by fatty acid transporters, such as FAT/CD36 and FATP1 (Koonen et al., 2005; Nickerson et al., 2009), and overexpression of which could promote intracellular fatty acid uptake (Ibrahimi et al., 1999; Sebastián et al., 2009). In the present study, betaine significantly down-regulated the mRNA expression level of FATP1, indicating that betaine might reduce the uptake of fatty acid. It is well known that ACC and FAS are the rate-limiting enzymes for fatty acid de novo synthesis (Liu et al., 1994; Smith et al., 2003). The nuclear transcription factors including SREBP1c and PPARγ are extremely associated with lipogenic genes (Farmer, 2005; Li et al., 2017b). SREBP1c can up-regulate the expression level of ACC (Stoeckman and Towle, 2002), whereas PPARγ suppresses HSL gene expression level (Grindflek et al., 2000). In the present study, the mRNA expression levels of ACC, FAS, SREBP1c, and PPARγ were all decreased significantly in the finishing mini-pigs fed betaine or glycine (Du et al., 2018). However, these results were inconsistent with previous research which dietary supplementation with betaine increased the mRNA levels of ACC and PPARγ in LD muscle (Li et al., 2017a). The conflict can be explained due to different breed, gender, feeding cycles and experiment stages, etc. Meanwhile, HSL and CPT1B were the rate-limiting enzymes of lipid catabolism (Mersmann, 1998; Peffer et al., 2005). Between them, the role of HSL is to hydrolyze triglycerides, and CPT1B is responsible for transporting fatty acids into mitochondria for oxidation. Previous experiments showed that betaine could enhance the mRNA expression levels of HSL and CPT1B (Li et al., 2017a; Albuquerque et al., 2017), which were also observed in our study. The results indicated that betaine heightened the catabolism of fatty acids in skeletal muscle tissue. In view of the foregoing, the reduction of IMF content and FFA in finishing pigs fed with betaine and glycine might be that dietary betaine and glycine both inhibited the uptake and synthesis of fatty acids and enhanced the catabolism of fatty acids in LD muscle tissue.

5. Conclusion

In summary, diets supplemented with 0.25% betaine could improve growth performance, carcass trait, pork quality and lipid metabolism of Huan Jiang finishing mini-pigs, and equimolar amounts of glycine could also improve meat quality and lipid metabolism of the finishing pigs to some extent, but was inferior to betaine. Therefore, we consider that betaine could partially replace glycine in finishing pig feeding. Besides, this study will also provide reference value for the further application of betaine in animal husbandry and human nutrition.

Author contributions

Yinzhao Zhong and Zhaoming Yan performed the sample measurements. Yinzhao Zhong, Bo Song and Changbing Zhen conducted the animal feeding and sampling. Yehui Duan, Jinping Deng and Xiangfeng Kong analyzed data and revised the manuscript. Fengna Li designed the trial and provided financial support. All authors have read and agreed the final manuscript.

Conflict of interest

We declare that we have no financial and personal relationships with other people or organizations that might inappropriately influence our work, and there is no professional or other personal interest of any nature or kind in any product, service and/or company that could be construed as influencing the content of this paper.