Skip to main content
Log in

Renal Protective Effects of Extracts from Guava Fruit (Psidium guajava L.) in Diabetic Mice

  • Original Paper
  • Published:
Plant Foods for Human Nutrition Aims and scope Submit manuscript

An Erratum to this article was published on 07 September 2012

Abstract

This study analyzed the content of phenolic acids and flavonoids in extracts of guava fruit (Psidium guajava L.), and examined the renal protective effects of guava aqueous extract (GAE) and ethanol extract (GEE) in diabetic mice. GAE had more caffeic acid, myricetin, and quercetin; and GEE had more cinnamic, coumaric and ferulic acids. GAE or GEE at 1 and 2 % was supplied in diet for 12 weeks. GAE or GEE intake at 2 % significantly reduced glucose and blood urea nitrogen levels, increased insulin level in plasma of diabetic mice (p < 0.05). GAE or GEE treatments dose-dependently reserved glutathione content, retained activity of catalase and glutathione peroxidase, and decreased reactive oxygen species, interleukin (IL)-6, tumor necrosis factor-α and IL-1β levels in kidney (p < 0.05). GAE and GEE treatments at 2 % significantly declined renal N ε-(carboxymethyl)lysine, pentosidine and fructose levels (p < 0.05), and suppressed renal activity of aldose reductase (p < 0.05). These findings support that guava fruit could protect kidney against diabetic progression via its anti-oxidative, anti-inflammatory and anti-glycative effects.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

AGE:

Advanced glycation endproduct

AR:

Aldose reductase

CML:

N ε-(carboxymethyl)lysine

Cr:

Creatinine

IL-6:

Interleukin-6

GPX:

Glutathione peroxidase

GSSG:

Oxidized glutathione

ROS:

Reactive oxygen species

SOD:

Superoxide dismutase

TNF-α:

Tumor necrosis factor-α

References

  1. Jawaheer B, Goburdhun D, Ruggoo A (2003) Effect of processing and storage of guava into jam and juice on the ascorbic acid content. Plant Foods Hum Nutr 58:1–12

    Article  Google Scholar 

  2. Mahattanatawee K, Manthey JA, Luzio G, Talcott ST, Goodner K, Baldwin EA (2006) Total antioxidant activity and fiber content of select Florida-grown tropical fruits. J Agric Food Chem 54:7355–7363

    Article  CAS  Google Scholar 

  3. Soman S, Rauf AA, Indira M, Rajamanickam C (2010) Antioxidant and antiglycative potential of ethyl acetate fraction of Psidium guajava leaf extract in streptozotocin-induced diabetic rats. Plant Foods Hum Nutr 65:386–391

    Article  CAS  Google Scholar 

  4. Shen SC, Cheng FC, Wu NJ (2008) Effect of guava (Psidium guajava Linn.) leaf soluble solids on glucose metabolism in type 2 diabetic rats. Phytother Res 22:1458–1464

    Article  Google Scholar 

  5. Huang CS, Yin MC, Chiu LC (2011) Antihyperglycemic and antioxidative potential of Psidium guajava fruit in streptozotocin-induced diabetic rats. Food Chem Toxicol 49:2189–2195

    Article  CAS  Google Scholar 

  6. Shah IM, Mackay SP, McKay GA (2009) Therapeutic strategies in the treatment of diabetic nephropathy - A translational medicine approach. Curr Med Chem 16:997–1016

    Article  CAS  Google Scholar 

  7. Graves DT, Kayal RA (2008) Diabetic complications and dysregulated innate immunity. Front Biosci 13:1227–1239

    Article  CAS  Google Scholar 

  8. Navarro-González JF, Mora-Fernández C (2008) The role of inflammatory cytokines in diabetic nephropathy. J Am Soc Nephrol 19:433–442

    Article  Google Scholar 

  9. Sato T, Iwaki M, Shimogaito N, Wu X, Yamagishi S, Takeuchi M (2006) TAGE (toxic AGEs) theory in diabetic complications. Curr Mol Med 6:351–358

    Article  CAS  Google Scholar 

  10. Lin CY, Tsai SJ, Huang CS, Yin MC (2011) Antiglycative effects of protocatechuic acid in the kidneys of diabetic mice. J Agric Food Chem 59:5117–5124

    Article  CAS  Google Scholar 

  11. Zapata S, Dufour JP (1992) Ascorbic, dehydroascorbic and isoascorbic acid simultaneous determinations by reverse phase ion interaction HPLC. J Food Sci 57:506–511

    Article  CAS  Google Scholar 

  12. Sreelatha S, Padma PR (2009) Antioxidant activity and total phenolic content of Moringa oleifera leaves in two stages of maturity. Plant Foods Hum Nutr 64:303–311

    Article  CAS  Google Scholar 

  13. Sellappan S, Akoh CC, Krewer G (2002) Phenolic compounds and antioxidant capacity of Georgia-grown blueberries and blackberries. J Agric Food Chem 50:2432–2438

    Article  CAS  Google Scholar 

  14. Schaffer AA, Aloni B, Fogelman E (1987) Sucrose metabolism and accumulation in developing fruit of Cucumis. Phytochemistry 26:1883–1887

    Article  CAS  Google Scholar 

  15. Lowry OH, Rosebrough NJ, Farr AL (1951) Protein determination with the Folin phenol reagent. J Biol Chem 193:265–275

    CAS  Google Scholar 

  16. Hsu CC, Lin CC, Liao TS, Yin MC (2006) Protective effect of s-allyl cysteine and spropyl cysteine on acetaminophen-induced hepatotoxicity in mice. Food Chem Toxicol 44:393–397

    Article  CAS  Google Scholar 

  17. Chao CY, Mong MC, Chan KC, Yin MC (2010) Anti-glycative and anti-inflammatory effects of caffeic acid and ellagic acid in kidney of diabetic mice. Mol Nutr Food Res 54:388–395

    Article  CAS  Google Scholar 

  18. Nishinaka T, Yabe-Nishimura C (2001) EGF receptor-ERK pathway is the major signaling pathway that mediates upregulation of aldose reductase expression under oxidative stress. Free Radic Biol Med 31:205–216

    Article  CAS  Google Scholar 

  19. Jain N, Dhawan K, Malhotra S, Singh R (2003) Biochemistry of fruit ripening of guava (Psidium guajava L.): Compositional and enzymatic changes. Plant Foods Hum Nutr 58:309–315

    Article  CAS  Google Scholar 

  20. Dixit Y, Kar A (2010) Protective role of three vegetable peels in alloxan induced diabetes mellitus in male mice. Plant Foods Hum Nutr 65:284–289

    Article  CAS  Google Scholar 

  21. Jung EH, Kim SR, Hwang IK, Ha TY (2007) Hypoglycemic effects of a phenolic acid fraction of rice bran and ferulic acid in C57BL/KsJ-db/db mice. J Agric Food Chem 55:9800–9804

    Article  CAS  Google Scholar 

  22. Busik JV, Mohr S, Grant MB (2008) Hyperglycemia-induced reactive oxygen species toxicity to endothelial cells is dependent on paracrine mediators. Diabetes 57:1952–1965

    Article  CAS  Google Scholar 

  23. Tsai SJ, Huang CS, Mong MC, Kam WY, Huang HY, Yin MC (2012) Anti-inflammatory and antifibrotic effects of naringenin in diabetic mice. J Agric Food Chem 60:514–521

    Article  CAS  Google Scholar 

  24. Koukoulitsa C, Zika C, Geromichalos GD, Demopoulos VJ, Skaltsa H (2006) Evaluation of aldose reductase inhibition and docking studies of some secondary metabolites, isolated from Origanum vulgare L. ssp. hirtum. Bioorg Med Chem 14:1653–1659

    Article  CAS  Google Scholar 

  25. Urios P, Grigorova-Borsos AM, Sternberg M (2007) Flavonoids inhibit the formation of the cross-linking AGE pentosidine in collagen incubated with glucose, according to their structure. Eur J Nutr 46:139–146

    Article  CAS  Google Scholar 

Download references

Acknowledgments

This study was supported by a grant from China Medical University, Taichung City, Taiwan (CMU100-ASIA-01).

Conflict of interest

The authors declare that they have no conflict of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Mei-Chin Yin.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lin, CY., Yin, MC. Renal Protective Effects of Extracts from Guava Fruit (Psidium guajava L.) in Diabetic Mice. Plant Foods Hum Nutr 67, 303–308 (2012). https://doi.org/10.1007/s11130-012-0294-0

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11130-012-0294-0

Keywords

Navigation