Open Access

The effect of melanin-free extract from Sepia esculenta ink on lipid peroxidation, protein oxidation and water-holding capacity of tilapia fillet during cold storage

Chemistry Central Journal201812:30

Received: 12 December 2017

Accepted: 9 March 2018

Published: 14 March 2018



Preservative effect of melanin-free extract of Sepia esculenta ink (MFESI) on Sparus latus fillet has been verified in our previous work. This study aims to further approach the mechanism of MFESI for extending the shelf-life of fish fillet during cold storage. Tilapia fillets were treated with different dosage of MFESI (0, 15, 25 and 35 mg/ml) and packed with preservative film for succedent cold-storage at 4 °C for scheduled time. Contents of total volatile basic nitrogen and sulfydryl and carbanyl groups were measured for evaluating protein oxidation. Malondialdehyde contents were measured for estimating lipid peroxidation and loss of water was used to determine water-holding capacity of fillet.


The data indicated that MFESI not only possessed certain degree of antioxidant capacity in vitro, also lengthened shelf-life of tilapia fillet in cold-storage condition. Apart from 15 mg/ml, both 25 and 35 mg/ml of MFESI obviously prevented lipid and protein from oxidation and reduced loss of water from tilapia fillets, and the latter was more effective than the former.


MFESI can repress lipid peroxidation and protein oxidation and reduce water loss, maintain the tilapia fillets quality and, thus, it could be an effective and natural preservative for extending the shelf-life of tilapia fillets during cold storage.


AntioxidationCold storage Sepia esculenta inkTilapia fillets


As a delicious food and a good resource of proteins in human diet, fish plays an important role in the global food supply. However, fish is difficult to keep fresh and even highly perishable due to the actions of microorganisms and enzymes naturally present and rancidity of the lipids. In order to keep the quality of fish, a lot of techniques to reduce the deterioration have been developed. Although the chemical preservatives are efficient and cheap, their health hazards are the concerns of consumers and regulations and the addition of synthetic preservatives has been restricted. Nowadays, the applications of safe and natural-source preservatives in the fish processing are still limited. Therefore, it is an urgent task to develop efficient, safe and natural preservatives for fish processing industry.

Sepia ink is a marine material with multifunctional roles based on its bioactive components, including protein, melanin and glycosaminoglycan [1]. Regrettably sepia ink is generally discarded during the fish process. To fully utilize the by-product of squid processing, attempts have been made by researchers. The potential fresh-keeping effects of sepia ink were approached in shiokara and peeled shrimp in earlier studies [26]. Similarly, our previous work also revealed the fresh-keeping effects of sepia ink. A melanin-free extract from sepia ink (MFESI) had demonstrated a capacity for significant prolongation of shelf-life on Sparus latus fillet and its preservative effect was revealed to be correlated with the suppression of oxidation and the spoilage microorganisms [79].

Tilapia is an economic and globally important aquaculture food commodity [10]. In 2015, the world aquaculture production of tilapia amounted 5,670,981 t (FAO, 2017). For this reason, tilapia was selected as experimental material in this research for investigation of the preservative mechanisms of sepia ink extract and its fresh-keeping effects on freshwater fish during cold storage, through comprehensive evaluations on lipid peroxidation, protein oxidation and water holding capacity in tilapia fillets.


Preparation of melanin-free extract from sepia ink

The extracting procedure was modified slightly according to our reported methods [8] and described as follows. Fresh ink taken from cuttlefish sacs (Sepia esculenta) was stored at − 70 °C for subsequent use. Before extraction, the frozen ink was thawed at 4 °C followed by dilution with phosphate buffered solution (PBS, pH 7.2) and sonication. The mixture was stored at 4 °C for more than 8 h and then was subjected to be centrifuged at 4 °C, 8000 rpm for 50 min. Supernatant was centrifuged for three times and then was harvested to be heated in 50 °C water bath for 1 h. The melanin-free extract was dialyzed to remove chemicals and was concentrated in turn with rotary evaporator. The concentrated extract was determined to be 35 mg/ml (high concentration, H) using drying method, and was then diluted to the other different concentrations with distilled water, 25 mg/ml (middle concentration, M) and 15 mg/ml (low concentration, L).

Sampling and treatment

Fresh tilapias (purchased from local aquaculture market in Zhanjiang, China) were sacrificed and the ridge meat was used to prepare fillets (1 cm × 2 cm × 3 cm). Fillets were washed with ice-cold normal saline and were then immersed in different concentrations of MFESI for 5 min respectively (m/v, 1/3). Drained fillets were packed with preservative film and were stored at 4 °C for the following determination.

Antioxidant capacity assay

Scavenging activity of hydroxyl free or DPPH (1,1-diphenyl-2-picrylhydrazyl) radical was determined according to the previously described methods [11].

DPPH radical: 2 ml of DPPH solution (0.1 mmol/l) was mixed with 0.5 ml of MFESI (35 mg/ml) and 1.5 ml H2O, and was then kept for 30 min at ambient temperature. Optical density value was read at 517 nm.
$$Scavenging\;activity\;\; (\% ) = \frac{{1 - (OD_{2} - OD_{1} )}}{{OD_{0} }} \times 100\%$$

OD0: DPPH, ethanol; OD1: ethanol, MFESI and water; OD2: DPPH-ethanol, MFESI and water.

Hydroxyl free radical: 1 ml of sample solution (0.125–1 mg/ml) in PBS (0.02 mol/l, pH 7.4) was mixed with 1.5 ml of 1,10-phenanthroline (1 mmol/l), 1 ml of FeSO4 (1.5 mmol/l), 1 ml of H2O2 (1%) and 3.5 ml of ultra pure water. After incubation for 60 min at 37 °C, optical density was read at 536 nm. Scavenging rate (%) was calculated according to the formula.
$$Scavenging\;activity \;\;(\% ) = \frac{{OD_{2} - OD_{1} }}{{OD_{0} - OD_{1} }} \times 100\%$$

OD1: no sample; OD0: no sample and H2O2; OD2: sample.

Biochemical assay

Total volatile basic nitrogen (TVB-N) content was determined according to the previously described method [12]. Contents of sulfhydryl group, carbanyl group and malondialdehyde (MDA) were measured with detection kits developed by a bioengineering institute in China according to manufacturer’s protocol.

Water-holding capacity

Water-holding capacity (WHC) was determined with the method of Lakshmanan et al. [13] that was slightly modified and described briefly as follows. Two grams of fish mince was placed into Eppendorf tube that has been placed in two pieces of filter paper and been weighed. Tube was centrifuged at 10 °C, 3000 rpm for 10 min, and then filter paper was weighed again. WHC (%) of fish meat was expressed as: 1 – 100% × (m2 − m1)/m.

m2: quality of centrifuged filter paper; m1: quality of uncentrifuged filter paper; m: quality of uncentrifuged fish meat (2.00 ± 0.01).

Data analysis

Data were expressed as the mean ± standard deviation. Differences between groups were analyzed by one-way ANOVA using the JMP statistical software. p < 0.05 was considered to be significant level.


In vitro antioxidant capacity of MFESI

Antioxidant capacity of MFESI was determined in vitro, and the result showed that, when the dosage of MFESI was 35 mg/ml, the scavenging rate of hydroxyl free radical and DPPH radical were 25.77 and 32.64%, respectively (Table 1).
Table 1

In vitro antioxidant capacity of MFESI (35 mg/ml, n = 5)


Antioxidant capicity

Scavenging activity of hydroxyl free radical (%)

25.77 ± 1.30

Scavenging activity of DPPH radical (%)

32.64 ± 2.09

TVB-N in fillet was reduced by MFESI

Total volatile basic nitrogen (TVB-N) of tilapia fillets was observed under the treatments with MFESI in different dosages along the experimental proceeding time. The results showed that the TVB-N values increased with the prolongation of proceeding time and raising of dosage (Table 2). However, in all of the observed samples, no significant decrease of TVB-N value was found within 48 h, while there was an obvious reduction of TVB-N in high dosage after 48 h.
Table 2

Inhibition of TVBN production by MFESI in fillets


0 h

24 h

48 h

72 h

96 h

120 h

144 h


3.78 ± 0.67a

5.67 ± 0.32a

13.23 ± 0.84a*

16.80 ± 1.03a*

18.90 ± 0.99a*

23.80 ± 0.84a*

26.13 ± 1.12a*


3.36 ± 0.39a

5.67 ± 0.70a

11.97 ± 0.89ab*

16.33 ± 0.81a*

17.73 ± 1.71a*

24.27 ± 1.17a*

25.20 ± 0.56ab*


3.36 ± 0.42a

5.04 ± 0.36a

10.08 ± 0.71b*

15.40 ± 1.98a*

17.27 ± 1.82a*

20.07 ± 0.81b*

23.33 ± 1.17b*


3.78 ± 0.76a

4.41 ± 0.79a

7.14 ± 0.89c*

10.27 ± 1.62b*

9.80 ± 1.19b*

14.00 ± 0.79c*

17.27 ± 1.14c*

Data represent the mean ± SD, n = 10. Vehicle, L, M and H express that the fillets has been treated with 0, 15, 25 and 35 mg/ml of MFESI, respectively. Different letters indicate significant between-group differences, abc p < 0.05. Asterisk expresses significant intra-group differences compared to the treated sample with MFESI for 0 h, * p < 0.05

Lipid peroxidation in fillet was suppressed by MFESI

Data in Table 3 shows increased MDA contents in the fillets treated with MFESI. In all of treated fillets, MDA contents after 48 h of the treating time were higher than that within the first 2 days. From 96 h, significant differences were also observed between fillets treated with vehicle and MFESI, especially with the high dosage of MFESI, suggesting that the inhibition of lipid peroxidation by MFESI occurred in the fillets.
Table 3

Inhibition of MDA production by MFESI in fillets


0 h

24 h

48 h

72 h

96 h

120 h

144 h


0.10 ± 0.02a

0.15 ± 0.02a

0.39 ± 0.03a*

0.41 ± 0.03a*

0.75 ± 0.02a*

0.91 ± 0.05a*

0.94 ± 0.05a*


0.09 ± 0.04a

0.14 ± 0.03a

0.36 ± 0.04a*

0.41 ± 0.02a*

0.69 ± 0.06ab*

0.65 ± 0.05b*

0.67 ± 0.02b*


0.09 ± 0.05a

0.13 ± 0.02a

0.38 ± 0.03a*

0.38 ± 0.02a*

0.59 ± 0.07b*

0.57 ± 0.03b*

0.66 ± 0.04ab*


0.09 ± 0.03a

0.11 ± 0.04a

0.37 ± 0.03a*

0.39 ± 0.06a*

0.39 ± 0.03c*

0.41 ± 0.05c*

0.45 ± 0.05b*

Data represent the mean ± SD, n = 10. Vehicle, L, M and H express that the fillets has been treated with 0, 15, 25 and 35 mg/ml of MFESI, respectively. Different letters indicate significant between-group differences, abc p < 0.05. Asterisk expresses significant intra-group differences compared to the treated sample with MFESI for 0 h, * p < 0.05

Protein oxidation in fillet was inhibited by MFESI

Formation of carbonyl compounds was employed to estimate the protein oxidation of the fillets in the current study. As the results shown in Table 4, tilapia fillets treated with MFESI exhibited significantly lower carbonyl contents than those treated with only vehicle, and the reductions of the carbonyl contents were more obvious at the higher MFESI concentrations. The carbonyl contents in fillets of each group were observed increasing gradually with the time, whilst the incremental degrees were remarkably different between the groups of fillets. Carbonyl contents in fillets treated with vehicle and low dosage of MFESI pronouncedly increased from 24 h of treating time, whereas the increases of carbonyl content in middle and high dosage groups were only visible after 48 and 96 h, respectively.
Table 4

Inhibition of carbanyl group production by MFESI in fillets


0 h

24 h

48 h

72 h

96 h

120 h

144 h


0.38 ± 0.03a

0.71 ± 0.03a*

0.82 ± 0.06a*

1.01 ± 0.02a*

1.17 ± 0.06a*

1.61 ± 0.09a*

2.11 ± 0.09a*


0.35 ± 0.04a

0.75 ± 0.06a*

0.76 ± 0.03a*

1.03 ± 0.11a*

1.33 ± 0.07a*

1.49 ± 0.10ab*

1.85 ± 0.09b*


0.36 ± 0.05a

0.56 ± 0.09ab

0.75 ± 0.07a*

0.78 ± 0.07b*

0.80 ± 0.05b*

1.27 ± 0.06b*

1.36 ± 0.08c*


0.35 ± 0.06a

0.45 ± 0.07b

0.52 ± 0.04b

0.58 ± 0.06c

0.70 ± 0.05b*

0.73 ± 0.08c*

0.95 ± 0.05d*

Data represent the mean ± SD, n = 10. Vehicle, L, M and H express that the fillets has been treated with 0, 15, 25 and 35 mg/ml of MFESI, respectively. Different letters indicate significant between-group differences, abcd p < 0.05. Asterisk expresses significant intra-group differences compared to the treated sample with MFESI for 0 h, * p < 0.05

The changes of total and protein sulphydryl group contents were also observed (Tables 5 and 6). The results showed that the total and protein sulphydryl group contents were found decreased with treating time. The reductions, however, were effectively retarded by MFESI in a dose-dependent manner from 24 h (vehicle and low dosage), 48 h (middle dosage) and 96 h (high dosage), respectively.
Table 5

Inhibition of protein sulfhydryl group reduction by MFESI in fillets


0 h

24 h

48 h

72 h

96 h

120 h

144 h


16.52 ± 0.41a

14.43 ± 0.38a*

12.94 ± 0.17a*

12.05 ± 0.44a*

9.86 ± 0.55a*

8.43 ± 0.48a*

9.60 ± 0.48a*


16.76 ± 0.27a

14.86 ± 0.20a*

13.35 ± 0.78a*

13.01 ± 0.84a*

12.14 ± 0.41b*

10.60 ± 0.69b*

10.21 ± 0.23a*


16.59 ± 0.58a

15.88 ± 0.41ab

15.11 ± 0.68b*

14.05 ± 0.32ab*

12.99 ± 0.59b*

12.74 ± 0.59c*

12.37 ± 0.74b*


16.51 ± 0.37a

16.27 ± 0.52b

15.98 ± 0.84b

15.37 ± 0.56b

14.89 ± 0.20c*

14.41 ± 0.61d*

14.51 ± 0.66c*

Data represent the mean ± SD, n = 10. Vehicle, L, M and H express that the fillets has been treated with 0, 15, 25 and 35 mg/ml of MFESI, respectively. Different letters indicate significant between-group differences, abcd p < 0.05. Asterisk expresses significant intra-group differences compared to the treated sample with MFESI for 0 h, * p < 0.05

Table 6

Inhibition of total sulfhydryl group reduction by MFESI in fillets


0 h

24 h

48 h

72 h

96 h

120 h

144 h


18.03 ± 0.54a

15.39 ± 0.32a*

14.95 ± 0.78a*

14.44 ± 0.73a*

14.21 ± 0.60a*

11.36 ± 0.67a*

12.26 ± 0.54a*


18.33 ± 0.56a

15.88 ± 0.34ab*

15.10 ± 0.08ab*

14.92 ± 0.91a*

14.41 ± 0.76a*

13.57 ± 0.84b*

13.01 ± 0.77a*


18.53 ± 0.72a

17.37 ± 0.64bc

16.96 ± 0.50bc*

15.47 ± 0.29a*

14.58 ± 0.36a*

13.91 ± 0.29b*

13.08 ± 0.27a*


18.22 ± 0.42a

17.94 ± 0.25c

17.14 ± 0.84c

16.59 ± 0.37b

16.18 ± 0.40b*

15.65 ± 0.41c*

14.89 ± 0.29b*

Data represent the mean ± SD, n = 10. Vehicle, L, M and H express that the fillets has been treated with 0 mg/ml, 15 mg/ml, 25 mg/ml and 35 mg/ml of MFESI, respectively. Different letters indicate significant between-group differences, abc p < 0.05. Asterisk expresses significant intra-group differences compared to the treated sample with MFESI for 0 h, * p < 0.05

Loss of water-holding capacity was prevented in MFESI-treated fillet

WHCs of fillets treated with vehicle and different doses of MFESI (L, M and H) were determined, respectively, as shown in Fig. 1. The results exhibited an improvement of WHC along with the dosage increase of MFESI (p < 0.05). In comparison with vehicle, high dosage of MFESI harvested the most effective protection on WHC demonstrated by data at 48 h (p < 0.05) and the later treating time (p < 0.05). However, the visible difference was dedicated from 72 h (p < 0.05) in middle dosage of MFESI. Moreover, low dosage of MFESI failed to rescue the WHC decline. In addition, it can be found that there was more increase of WHC in the high dose treatment group than that in the middle dose group from 96 h.
Fig. 1

Loss of water-holding capacity of fillet was repressed by MFESI. Vehicle, L, M and H express that the fillets has been treated with 0, 15, 25 and 35 mg/ml of MFESI, respectively. *p < 0.05 expresses the difference compared to vehicle treated fillet; #p < 0.05, vs low dosage of MFESI (15 mg/ml) treated fillet

Correlation among the indicators

In order to reveal relationships among the detected variables in tilapia fillets treated with high dosage of MFESI, Pearson correlation coefficients were analyzed and showed in Table 7. The results indicated strong relationships (p < 0.01) among lipid peroxidation, protein oxidation and water-holding capacity in MFESI-treated tilapia fillet during cold storage.
Table 7

Pearson correlation coefficients between measured variables



Protein sulfhydryl

Carbanyl group




− 0.94**


− 0.97**



− 0.85**


− 0.89**

Protein sulfhydryl


− 0.93**


Carbanyl group


− 0.98**

Asterisk expresses significant difference between the two intersection indicators, **p < 0.01


Sepia ink has been proved to be a multifunctional marine material containing melanin, lipid, protein, polysaccharide and microelements [14]. The sepia ink polysaccharides (SIP) from Sepia esculenta ink is categorized as glycosaminoglycan mainly consisted of arabinose and aminogalactose [15]. MFESI and SIP have been proved to have antioxidant activity by our previous work based on in vivo and in vitro investigations, such as scavenging hydroxyl free radical and DPPH radical, preventing DNA from damage induced by H2O2 and ultraviolet radiation [1619]. DPPH is a synthetic, stable free-radical containing three benzene rings and a lone electron in a nitrogen atom [20]. Aubergine DPPH captures a hydrogen atom from antioxidant to form yellow unfree DPPH-H [21]. In MFESI solution, many constituents, including polysaccharide, protein, lipid and melanin, can provide hydrogen. Consequently, DPPH was deleted by MFESI. And, higher concentration of MFESI provided more hydrogen, so antioxidant capacity increased with rising concentration of MFESI.

Hydroxyl radical is the most active one of reactive oxide species and reacts with biological macromolecules, such as protein, lipid and DNA through hydrogen abstraction, addition and electron transfer mechanisms [22]. We previously found that DNA breakage induced by hydroxyl originated from H2O2 exposed to UV can be prevented by SIP via inhibiting the activation of H2O2 by UV [17]. In this study, with the addition of MFESI into the Fenton reaction system, the reduction of hydroxyl radical content might correlate with suppression of Fenton reaction. However the accurate mechanism should be explained in the following work.

It is well known that oxidants, such as radicals, can lead to destruction of protein and lipid, resulting in cytolysis, which is a critical cause for shortening shelf-life of preserved food, especially fishes with large amount of polyunsaturated fatty acids. Our report revealed fresh-keeping effect of MFESI on marine fish demonstrated by elongated shelf-life that resulted from inhibition of bacteria growth and protein degradation [8].

Total volatile basic nitrogen (TVBN) is a group of nitrogen-containing compounds, including NH3 and amines, originated from protein degradation by enzymes and bacteria [23]. This study showed significant reduction of TVBN by MFESI in tilapia fillet during cold storage, which could be explained by the following mechanisms. Firstly, inhibition of bacteria by MFESI blocked protein degradation [8]. Secondly, SIP activated Nrf2/ARE pathway, an important antioxidation-associated signaling pathway, to delete oxidants [24]. Thirdly, SIP can prevent effectively cells from oxidants induced autophagy, ameliorating formation of autophagosome [15, 25]. Therefore, in our current research, a possible mechanism was that the liberation of hydrolases from lysosomes was inhibited by SIP, so that the degradation of protein and the formation of TVBN were weakened.

Apart from TVBN, two indicators of protein disruption are loss of sulphydryl group and production of carbanyl group. Determination of carbonyl is considered as a routine procedure for evaluating protein oxidation, but it is not very accurate to estimate the status of protein oxidation due to the presence of various originated carbonyls, such as derivatization agent and lipid-derived carbonyls [26]. Reactive oxygen, such as hydroxyl radical, can break peptide bond to form carbonyl [27]. Hydroxyl radicals were scavenged by MFESI, resulting in inhibition of production of carbonyl from proteins. Another indicator as a complementary technique of protein oxidation is loss of sulphydryl group of protein due to formation of disulphide bond, which partly results from lipid oxidation. NO induces nitrosation of protein sulfydryl, reducing protein sulfydryl that can be also caused by other oxidants [28]. SIP can reduce NO via activating Nrf2/ARE signaling pathway [24, 29, 30]. Therefore, MFESI decreased NO and oxygen radical contents, protecting protein from oxidation and consequently repressing increase of carbonyl and decrease of sulfydryl.

Additionally, lipid peroxidation is both a promoter of protein oxidation and another important cause of reducing quality and shelf-life of meats. Sepia ink and SIP possess antioxidant activities [1619, 24, 31], which prevents lipid from oxidants mediated peroxidation [22]. As a secondary product and an indicator of lipid peroxidation, MDA content in fillet expresses degree of lipid oxidation. This study revealed that MFESI definitely inhibited lipid peroxidation in fillets, and the inhibition increased with the extract concentration.

Lipid oxidative products lead protein to oxidation degradation. Also, lipid oxidation and protein oxidation occur independently or parallel [32, 33]. Combining the data of lipid peroxidation and protein oxidation in tilapia fillets during cold storage, two important topics can be deduced reasonably. One is that MFESI definitely inhibited oxidation of lipid and protein. Another topic is that lipid peroxidation and protein oxidation occurred independently in the beginning stage (before 48 h). In the fillets treated with vehicle or low-dosage MFESI, protein oxidation was visible at 24 h whilst lipid peroxidation products were found at 48 h. Apparently, protein oxidation occurred before lipid peroxidation.

Aside from carbonyl formation and sulfhydryl reduction, protein oxidation brings about another outcome, alternation of water holding capacity (WHC). WHC expresses the capacity of muscle resisting water loss. There are two types of water forms, free and bound, accounting for 90 and 10%, respectively, in fish tissues. Free water can be influenced by various factors, such as protein structure and pH, and so on [13, 34]. Protein determines distribution of water in meat, affecting directly WHC of meat. Increase of WHC indicated that protein degradation was suppressed by MFESI during the cold-storage of fillet.

To further understand relationship among lipid peroxidation, protein oxidation and water-holding capacity, Pearson correlation was analyzed among all of the measured indicators in high dosage of MFESI treated fillets. The results indicated strong relationships among lipid peroxidation, protein oxidation and water-holding capacity in MFESI-administered tilapia fillet during cold storage.

Summarily, based on our previous findings about fresh-keeping effects of MFESI on marine fish, this study further investigated the involved mechanisms on freshwater fish through assessment of oxidation of lipid and protein, as well as WHC of fillets. Results revealed that MFESI prevented effectively fillets from protein oxidation and lipid peroxidation through eliminating radicals, WHC was maintained. Consequently, quality of fish meat was kept and shelf-time was extended undoubtedly. Sepia ink has a long history of being used in various ways in food and drugs [14], suggesting that it is edible safety. It is can be seen that MFESI is a potential natural preservative for fish and other foods.


Authors’ contributions

ZHD and HZL had full access to all of the data in the study and took responsibility for the integrity of the data and the accuracy of the data analysis. Study conception and design were provided by HZL and ZHD. Acquisition of data were completed ZHD, PL, YQL, YPG and HZL. Analysis and interpretation of data were conducted by ZHD, PL, YPG and YQL. All authors read and approved the final manuscript.


This work was jointly supported by the National Natural Science Foundation of China (Grant Nos. 31171667, 31360395), Guangxi talent highland of preservation and deep processing research in fruit and vegetables and Special Fund for Distinguished Experts in the Guangxi Zhuang Autonomous Region, China.

Competing interests

The authors declare that they have no competing interests.


All authors are involved in this research and drafting or revising the article and all authors approved the final version to be published.

Ethics approval and consent to participate

Not applicable.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

Institute of Food Science & Engineering Technology, Hezhou University, Hezhou, China
College of Chemistry & Environment, Guangdong Ocean University, Zhanjiang, China
College of Food Science & Technology, Guangdong Ocean University, Zhanjiang, China


  1. Zhong JP, Wang G, Shang JH, Pan JQ, Li K, Huang Y, Liu HZ (2009) Protective effects of squid ink extract towards hemopoietic injuries induced by cyclophosphamide. Mar Drugs 7:9–18View ArticleGoogle Scholar
  2. Takai M, Kawai Y, Inoeu N, Shinano H (1992) Comparative studies on microbiological and chemical characteristics of “ika-shiokara akazukuri” and “ika-shiokara kurozukuri”. Nippon Suisan Gakk 58:2373–2378View ArticleGoogle Scholar
  3. Takai M, Yamazaki K, Kawai Y, Inoeu N, Shinano H (1993) Effect of squid liver, skin, and ink on microbiological characteristics of “ika-shiokara” during ripening process. Nippon Suisan Gakk 59:1609–1615View ArticleGoogle Scholar
  4. Takai M, Yamazaki K, Kawai Y, Inoeu N, Shinano H (1993) Effect of squid liver, skin, and ink on microbiological characteristics of “ika-shiokara” during ripening process. Nippon Suisan Gakk 59:1917–1923Google Scholar
  5. Yasuhiro F, Katsuya F, Hidehiro K, Shugo W (2005) Improvement of “kurozukuri ika-shiokara” (fermented squid meat with ink) odor with Staphylococcus nepalensis isolated from the fish sauce mush of frigate mackerel Auxis rochei. Nippon Suisan Gakk 71:611–617View ArticleGoogle Scholar
  6. Sadok S, Abdelmoulah A, Abed AE (2004) Combined effect of sepia soaking and temperature on the shelf life of peeled shrimp Penaeus kerathurus. Food Chem 88:115–122View ArticleGoogle Scholar
  7. Wu JL, Luo JQ, Liu HZ, Wang G, Li WD, Xiao Y, Zhong JP, Pan JQ (2010) Fresh-keeping effects of cuttlefish ink polysaccharide on squid during cold storage. Food Sci 10:304–307Google Scholar
  8. Shi LS, Liu HZ, Zhong JP, Pan JQ (2015) Fresh-keeping effects of melanin-free extract from squid ink on Yellowfin Sea bream (Sparus latus) during cold storage. J Aquat Food Prod Technol 24:199–212View ArticleGoogle Scholar
  9. Shi LS, Liu HZ, Zhong JP, Xie ZL, Le XY, Huang ZC, Pan JQ (2012) Isolation of inhibitory compounds against marine fish derived putrefying bacteria from squid ink. Sci Technol Food Ind 11:120–123Google Scholar
  10. Carbonera F, Montanher PF, Figueiredo IL, Bonafé EG, Júnior OOS, Sargi SC, Gonçalves RM, Matsushita M, Visentainer JV (2016) Lipid composition and antioxidant capacity evaluation in tilapia fillets supplemented with a blend of oils and vitamin E. J Am Oil Chem Soc 93:1255–1264View ArticleGoogle Scholar
  11. Xie JH, Wang ZJ, Shen MY, Nie SP, Gong B, Li SH, Zhao Q, Li WJ, Xie MY (2016) Sulfated modification, characterization and antioxidant activities of polysaccharide from Cyclocarya paliurus. Food Hydrocolloid 53:7–15View ArticleGoogle Scholar
  12. Yusuf Ali M, Iqbal Sharif M, Adhikari RK, Faruque O (2010) Post mortem variation in total volatile base nitrogen and trimethylamine nitrogen between galda (Macrobrachium rosenbergii) and bagda (Penaeus monodon). Univ J Zool Rajshahi Univ 28:7–10Google Scholar
  13. Lakshmanan R, Parkinson JA, Piggott JR (2007) High-pressure processing and water-holding capacity of fresh and cold-smoked salmon (Salmo salar). LWT-Food Sci Technol 40:544–551View ArticleGoogle Scholar
  14. Derby CD (2014) Cephalopod ink: production, chemistry, functions and applications. Mar Drugs 12:2700–2730View ArticleGoogle Scholar
  15. Liu HZ, Tao YX, Luo P, Deng CM, Gu YP, Yang L, Zhong JP (2016) Preventive effects of a novel polysaccharide from Sepia esculenta ink on ovarian failure and its action mechanisms in cyclophosphamide-treated mice. J Agr Food Chem 64:5759–5766View ArticleGoogle Scholar
  16. Liu HZ, Luo P, Chen SH, Shang JH (2011) Effects of squid ink on growth performance, antioxidant functions and immunity in growing broiler chickens. Asian Austral J Anim Sci 24:1752–1756View ArticleGoogle Scholar
  17. Luo P, Liu HZ (2013) Antioxidant ability of squid ink polysaccharides as well as their protective effects on DNA damage in vitro. Afr J Pharm Pharmacol 7:1382–1388View ArticleGoogle Scholar
  18. Luo P, Shi LS, Liu HZ (2013) Antioxidant capacity of squid ink polysaccharide in vitro. Food Res Dev 34(8):1–4Google Scholar
  19. Vate NK, Benjakul S (2013) Antioxidative activity of melanin-free ink from splendid squid (Loligo formosana). Int Aquat Res 5:9View ArticleGoogle Scholar
  20. Eklund PC, Langgvik OK, Warna JP, Salmi TO, Willforc SM, Sjoholm RE (2005) Chemical studies on antioxidant mechanisms and free radical scavenging properties of lignans. Org Biomol Chem 3(18):3336–3347View ArticleGoogle Scholar
  21. Kumaran A, Joel karunakaran R (2006) Antioxidant and free radical scavenging activity of an aqueous extract of Coleus aromaticus. Food Chem 97(1):109–114View ArticleGoogle Scholar
  22. Fang YZ, Zheng RL (2002) Theory and application of free radical biology. Sci Press, BeijingGoogle Scholar
  23. Aksnes A, Brekken B (1988) Tissue degradation, amino acid liberation and bacterial decomposition of bulk stored capelin. J Sci Food Agr 45(1):53–60View ArticleGoogle Scholar
  24. Le XY, Luo P, Gu YP, Tao YX, Liu HZ (2015) Squid ink polysaccharide reduces cyclophosphamide-induced testicular damage via Nrf2/ARE activation pathway in mice. Iran J Basic Med Sci 18:827–831Google Scholar
  25. Gu YP, Yang XM, Luo P, Li YQ, Tao YX, Duan ZH, Xiao W, Zhang DY, Liu HZ (2017) Inhibition of acrolein-induced autophagy and apoptosis by a glycosaminoglycan from Sepia esculenta ink in mouse Leydig cells. Carbohyd Polym 163:270–279View ArticleGoogle Scholar
  26. Botsoglou E, Govaris A, Ambrosiadis I, Fletouris D, Botsoglou N (2014) Effect of olive leaf (Olea europea L.) extracts on protein and lipid oxidation of long-term frozen n-3 fatty acids-enriched pork patties. Meat Sci 98:150–157View ArticleGoogle Scholar
  27. Li PF, Fang YZ (1994) Effects of reactive oxygens on protein damage. Life Chem 14(6):1–3Google Scholar
  28. Huang B, Chen C (2012) Function and mechanism of nitric oxide (II): mechanism and protein s-nitrosation. Acta Biophysica Sinica 28(4):268–277View ArticleGoogle Scholar
  29. Turcanu V, Dhouib M, Poindron P (1998) Nitric oxide synthase inhibition by haem oxygenase decreases macrophage nitric-oxide-dependent cytotoxicity: a negative feedback mechanism for the regulation of nitric oxide production. Res Immunol 149:741–744View ArticleGoogle Scholar
  30. Siegel D, Ross D (2000) Immunodetection of NAD(P)H: quinine oxidoreductase 1 (NQO1) in human tissues. Free Rad Bio Med 29:246–253View ArticleGoogle Scholar
  31. Le XY, Luo P, Gu YP, Tao YX, Liu HZ (2015) Interventional effects of squid ink polysaccharide on cyclophosphamide-associated testicular damage in mice. Bratisl Med J 116:334–339View ArticleGoogle Scholar
  32. Grimsrud PA, Xie H, Griffin TJ, Bernlohr DA (2008) Oxidative stress and covalent modification of protein with bioactive aldehydes. J Biol Chem 283:21837–21841View ArticleGoogle Scholar
  33. Teets AS, Were LM (2008) Inhibition of lipid oxidation in refrigerated and frozen salted raw minced chicken breasts with electron beam irradiated almond skin powder. Meat Sci 80:1326–1332View ArticleGoogle Scholar
  34. Andersen CM, Rinnan A (2002) Distribution of water in fresh cod. LWT-Food Sci Technol 35:687–696View ArticleGoogle Scholar


© The Author(s) 2018