Journal List > J Korean Ophthalmol Soc > v.50(10) > 1008397

Kim and Oh: Effect of Glutathione With Sea Tangle Extract on Prevention of Selenite-Induced Cataract Formation in Rats

Abstract

Purpose

To evaluate antioxidative and preventive effects of sea tangle extract on selenite-induced cataract formation.

Methods

Eighty SD rat pups were randomized into 8 groups. Group 1 received no injection of reagent (normal); Group 2 to 8 received injection of selenite (15 μmol/Kg, s.c.) was injected. In group 2 (control) and group 3, normal saline (i.p.) and ascorbic acid (i.p.) was injected on days 3∼31. In groups 4∼8, sea tangle extract (i.p.) was injected at a concentration of 12.5, 25, 50, 100, 200 mg/kg, respectively. Development of cataract was assessed and photographed weekly under slit lamp. Rat lenses were analyzed for antioxidant enzymes, glutathione peroxidase (GPx), superoxide dismutase and malondialdehyde. Furthermore, an amino acid analysis of sea tangle extract was performed.

Results

Significant differences (p <0.05) were seen in cataract development in group 7. Dense nuclear cataracts developed in 8 of 10 of the control group (group 2); Group 4∼8 developed nuclear cataract with proportion of 6/10, 3/10, 2/10, 1/10, and 6/10 rats. In sea tangle injected group, levels of GPx were higher than in the ascorbic acid and control groups. In particular, group 7, injected with 100 mg/kg of sea tangle extract, showed significantly high level of enzyme. Results of the amino acid analysis showed sea tangle includes glutamate-glycine-cysteine, major constituents of glutathione (GSH).

Conclusions

The glutamate-glycine-cysteine in sea tangle is supposed to increase the level of lens GSH and this may contribute to lowering cataract development. This study strongly supports the activity of sea tangle as an endogenous antioxidant and anticataract agent.

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Figure 1.
Development selenite-induced cataract on the 4th day after sodium selenite injection. (A) External photograph of cataract development (B) Slit lamp photograph of cataract development. The central dense nuclerosclerosis cataract was found after sodium selenite injection.
jkos-50-1555f1.tif
Figure 2.
Slit lamp photograph of group 2 (control group) at the final follow-up (3 weeks after sodium selenite injection). Eight of 10 rats developed central nuclear cataract.
jkos-50-1555f2.tif
Figure 3.
Slit lamp photograph of group 7 (sea tangle extract 100 mg/kg injected) at the final follow-up (3 weeks after sodium selenite injection,). One of 10 rats developed central nuclear cataract as seen in the two top photographs and remaining 9 rats kept clear lenses as seen in the two bottom photographs.
jkos-50-1555f3.tif
Table 1.
The incidence of cataract development in each group. Group 7 (sea tangle extract 100 mg/kg) shows the lowest incidence of cataract. As the concentration of sea tangle extract is higher, the ratio of cataract development is getting lower. However, the incidence of cataract is getting high when the concentration is too low or too high (eg. Group 4 and 8)
Experimental groups No. of rats Number of rats in which lenticular opacification occurred Incidence (%)
Group 1 10 0 0
Group 2 10 8 80
Group 3 10 4 40
Group 4 10 6 60
Group 5 10 3 30
Group 6 10 2 20
Group 7* 10 1* 10*
Group 8 10 6 60

All values are expressed as mean± SD.

Group 1=normal rat pups, Group 2=Selenite+intraperitoneal (i.p) Saline injection, Control group, Group 3=Selenite+i.p Ascorbic acid 1,000 mg/kg injection, Group 4=Selenite+i.p Sea tangle extract 12.5 mg/kg injection, Group 5=Selenite+i.p Sea tangle extract 25 mg/kg injection, Group 6=Selenite+i.p Sea tangle extract 50 mg/kg injection, Group 7=Selenite+i.p Sea tangle extract 100 mg/kg injection, Group 8=Selenite+i.p Sea tangle extract 200 mg/kg injection.

* Statistically significant difference (p<0.05) when compared with group 2 (control group).

Table 2.
Quantitative analysis of antioxidant system enzymes and malondialdehyde in lenses of rats
Experimental groups Antioxidant enzymes
MDA (nmol/g)
GPx (nmol/min/ml) SOD (U/ml)
Group 1 293.41±12.3 62.20±7.3 60.5±3.7
Group 2 207.72±9.6 38.15±6.8 88.6±5.3
Group 3 210.55±11.2 44.75±8.3 76.2±6.2
Group 4 212.38±7.9 44.84±5.7 72.5±7.4
Group 5 209.91±8.5 46.71±11.6 74.1±6.8
Group 6 230.64±13.2* 50.10±9.3* 65.4±7.6*
Group 7 289.27±9.2* 52.95±8.9* 63.2±8.3*
Group 8 211.72±10.4 50.10±7.9* 69.7±4.8

All values are expressed as mean± SD.

GSH=glutathione peroxidase; SOD=superoxide dismutase; MDA=malondialdehyde.

* Statistically significant difference (p<0.05) when compared with group 2 (control group).

Table 3.
Amino acid analysis of sea tangle extract. Results of amino acid analysis show sea tangle includes glutamate, cysteine and glycine which are components of glutathione
Aminoacid Concentration (pMol, Sea tangle)
Glutamate 39309.89
Cysteine 235.16
Glycine 9862.75
Aspartic acid 12943.78
Serine 5864.74
Histidine 2170.83
Arginine 2818.02
Threonine 6370.93
Alanine 19275.18
Proline 7635.96
Tyrosine 1915.90
Valine 7717.76
Methionine 2788.05
Isoleucine 4998.95
Leucine 8667.01
Lysine 4834.98
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