THE EFFECTS OF EARTHWORMS’ (PHERETIMA ASPERGILLUM) ETHANOL EXTRACT TOWARD THE IMPROVEMENT OF NERVE FIBERS DENSITY IN DIABETIC ULCERS CARE DEGREE II OF RATS WISTAR

Authors

  • Heri Kristianto Brawijaya University
  • Ni Putu Jeny Mardiati Brawijaya University

Keywords:

Diabetic ulcer, earthworm (Pheretima aspergillum), nervous fibers density

Abstract

Background. Diabetic ulcer is a chronic complication of diabetes mellitus which lead to infection and lower extremity amputation. Earthworm (Pheretima aspergillum) has bioactive substance of IGF-1 (insulin like growth factor 1) to promote Schwann cell proliferation, survival, and migration into the distal end in the injured nerve area to support axonal re-growth.
Objective. To investigate the effect of earthworm extract (Pheretima aspergillum) on the enhancement of nervous fibers density in rats induced diabetic ulcer stage II.
Methods. This study applied a true-experimental posttest only controlled group design. Samples were divided into five groups: Normal Saline as a negative control group, Hydrogel as a positive control group, and the three treatment groups received earthworm extract via topical, oral, and topical-oral. The patterns of nervous fibers connecting to hair follicles were identified using silver impregnation stain.
Results. The result shows the groups receiving earthworm extract have significantly higher nervous fibers density compared to the control groups (p=0.000). The administered of earthworm extract via topical has an optimal effect on improving nervous fibers density.
Conclusion. Earthworm extract promote regeneration of peripheral nerve in rats model of diabetic.

References

ADA (American Diabetes Association). Diagnosis and Classification of Diabetes Mellitus. Diabetes Care, 2004; 27: 5-10.

Wild S, Roglic G, Green A, Sicree R, King H. Global Prevalence of Diabetes: Estimates for the Year 2000 and Projections for 2030. Diabetes Care, 2004; 27: 1047-1053.

Bos M, and Agyemang C. Prevalence and Complications of Diabetes Mellitus in Northern Africa, A Systematic Review. BMC Public Health, 2013; 1471-2458/13/387.

Clayton W, and Elasy TA. A Review of the Pathophysiology, Classification, and Treatment of Foot Ulcers in Diabetic Patients. Clinical Diabetes, 2009; 27 (2): 52-58.

Tesfaye S, and Gill G. Chronic Diabetic Complications in Africa. African Journal of Diabetes Medicine, 2011; 19: 4-8.

NLLIC (National Limb Loss Information Center). 2008. Diabetes and Lower Extremity Amputations. Amputee Coalition of America.

Bradbury S, and Price P. The Impact of Diabetic Foot Ulcer Pain on Patient Quality of Life. Wounds UK, 2011; 7: 32-49.

Chang, Yu Ming et al. Schwann Cell Migration Induced by Earthworm Extract via Activation of PAs and MMP2/9 Mediated through ERK1/2 and p38. Evidence-Based Complementary and Alternative Medicine, 2011; article ID 395458.

Chang, Yu Ming et al. RSC96 Schwann Cell Proliferation and Survival Induced by Dilong through PI3K/Akt Signaling Mediated by IGF-I. Evidence-Based Complementary and Alternative Medicine, 2011; articleID 216148.

Vincent AM, Russel JW, Low P, Feldman EL. Oxidative Stress in the Pathogenesis of Diabetic Neuropathy. Endocrine Reviews, 2004; 25 (4): 612-628.

Teppala S, and Shankar A. Association Between Serum IGF-1 and Diabetes Among U.S. Adults. Diabetes Care, 2010; 33 (10): 2257-2259.

Simpson, Hellen L et al. Insulin-Like Growth Factor I Has a Direct Effect on Glucose and Protein Metabolism, But No Effect on Lipid Metabolism in Type 1 Diabetes. The Journal of Clinical Endocrinology & Metabolism, 2004; 89(1): 425-432.

Saskatchewan Ministry of Health. Clinical Practice Guidelines for the Prevention and Management of Diabetes Foot Complications. Saskatchewan Health Quality Council; 2008.

Oyibo SO, Jude EB, Tarawneh I, Nguyen HC, Harkless LB, Boulton AJM. A Comparison of Two Diabetic Foot Ulcer Classification Systems. Diabetes Care, 2001; 24: 84–88.

Dealey, Carol. The Care of Wounds: A Guide for Nurses, 3rd Ed., Blackwell Publishing, Oxford, UK; 2005. p. 56-168.

Chen, Chao Tsung et al. Earthworm Extracts Facilitate PC12 Cell Differentiation and Promote Axonal Sprouting in Peripheral Nerve Injury. The American Journal of Chinese Medicine, 2010; 38 (3): 547-560

Mendes JJ, Leandro CI, Bonaparte DP, Pinto AL. A Rat Model of Diabetic Wound Infection for the Evaluation of Topical Antimicrobial Therapies. Comparative Medicine, 2012; 62(1): 37-48.

Zangiabadi, Nasser. Effects of Melatonin in Prevention of Neuropathy in STZ-Induced Diabetic Rats. American Journal of Pharmacology and Toxicology, 2011; 6(2):59-67.

Wu KK, and Huan Y. Streptozotocin-Induced Diabetic Models in Mice and Rats. Current Protocols in Pharmacology, 2008; 5.47.15.47.14.

Ukong S, Ampawong S, Kengkoom K. Collagen Measurement and Staining Pattern of Wound Healing Comparison with Fixations and Stains. Journal of Microscopy Society of Thailand, 2008; 22: 37-41.

Rizzo, DC. Delmar's Fundamentals of Anatomy & Physiology, Thomson Learning, New York; 2001. p. 120-121.

National Academy of Science. Guide for the Care and Use of Laboratory Animals, 8th Ed., Natinal Research Council, Washing-ton DC; 2010. p. 68-80.

Dahlan, MS. Statistik untuk Kedokteran dan Kesehatan Deskriptif, Bivariat dan Multivariat Dilengkapi dengan Menggunakan SPSS, Ed. 4, Salemba Medika, Jakarta. Indonesia; 2009, hal. 106-111.

Mucimapura S, Wattanathom J, Thongrong S, Chaisiwamongkol K, Sripanidkulchai B. Morusalba Enhanced Functional Recovery After Sciatic Nerve Crush Injury. American Journal of Agricultural and Biological Sciences, 2010; 5(3): 294-300.

Junqueira LC, and Carneiro J. Histologi Dasar: Teks & Atlas, Ed.10, Jan Tambayong (penterjemah), EGC, Jakarta, Indonesia; 2007. hal. 153-368.

Grisolia DF et al. Ultrastructure of the Myelinated and Unmyelinated Nerve Fibers of the Tongue Mucosa of Albinus Rat (Wistar) with Aging. Int. J. Morphol, 2006; 24 (3): 407412.

Diapath. Special Stains Handbook, Savoldini, Martinengo, Italy; 2013. p. 96-97.

Gagnon V, Larouche D, Bareil RP, Gingras M, Germain L, Berthod F. Hair Follicles Guide Nerve Migration In Vitro and In Vivo in Tissue-Engineered

Skin. Journal of Investigative Dermatology, 2011; 131: 1375-1378.

Negi G, Kumar A, Joshi RP, Ruby PK, Sharma SS. Oxidative Stress and Diabetic Neuropathy: Current Status of Antioxidants. The IIOAB Journal, 2011; 2 (6): 71-78.

Fernandez R, Griffiths R, Ussia C. Water for Wound Cleansing (Review), Cochrane Database of Systematic Reviews, 2010; Issue 2.

NANDA (North American Nursing Diagnosis Association) International. Diagnosis Keperawatan: Definisi dan Klasifikasi 20122014, Made Sumarwati dan Nike Budhi Subekti (penterjemah), EGC, Jakarta, Indonesia. 2012.

Kesavan R, Babu M, Viswanathan V. Clinical Efficacy and Cost Effectiveness of Cerdak Dressing Over Saline Gauze Dressing Among Diabetic Foot Ulcers, West Mada Church Street, Royapuram, Chennai; 2008. p. 1-22.

Jones V, Grey JE, Harding KG. Wound Dressing. BMJ, 2006; 332: 777-780.

Rainey, Joy. Wound Care: A Handbook for Community Nurses, Whurr Publishers, Philadelphia, USA; 2002. p.1-10.

Dumville JC, O’Meara S, Deshpande S, Speak K. Hydrogel Dressings for Healing Diabetic Foot Ulcers (Review), Cochrane Database of Systematic Reviews, 2013; Issue 7.

Boateng JS, Matthews KH, Stevens HNE, Eccleston GM. Wound Healing Dressings and Drug Delivery Systems: A Review. Journal of Pharmaceutical Sciences, 2008; 97 (8): 28922923.

Penn JW, Grobbelaar AO, Rolfe KJ. The Role of the TGF-β Family in Wound Healing, Burns and Scarring: a Review. Int J Burn Trauma, 2012; 2(1):18-28.

Parkinson, David B et al. Transforming Growth Factor β (TGFβ) Mediates Schwann Cell Death In Vitro and In Vivo: Examination of c-Jun Activation, Interactions with Survival Signals, and the Relationship of TGFβ-Mediated Death to Schwann Cell Differentiation. The Journal of Neuroscience, 2001; 21 (21): 8572-8585.

Antonio, Maurizio D et al. TGFβ Type II Receptor Signaling Controls Schwann Cell Death and Proliferation in Developing Nerves.

The Journal of Neuroscience, 2006; 26 (33):8417-8427.

Svennigsen AF, and Dahlin LB. Repair of the Peripheral Nerve—Remyelination that Works. Brain Sciences, 2013; 3: 1182-1197.

Gallagher EJ, Fierz Y, Ferguson RD, Leroith D, Pract E. The Pathway from Diabetes and Obesity to Cancer, on the Route to Targeted Therapy. Endocr Pract, 2010;16 (5): 864-873.

Omar HM, Ibraheim ZZ, El-Shimy NA, Ali RS. Anti-inflammatory, Antipyretic and Antioxidant Activities of the Earthworms Extract. Journal of Biology and Earth Sciences, 2012; 2 (1): 10-17.

Balamurugan M, Parthasarathi K, Cooper EL, Ranganathan LS. Earthworm Paste (Lampito mauritii, Kinberg) Alters Inflammatory, Oxidative, Haematological and Serum Biochemical Indices of Inflamed Rat. European Review for Medical and Pharmacological Sciences, 2007; 11: 77-90.

Anitha J, and Jayraaj IA. Nutritional and Antioxidant Evaluation of Earthworm Powder (Eudrillus euginae). International Research Journal of Pharmacy, 2012; 3 (2): 177-180.

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Published

2017-07-01

How to Cite

Kristianto, H., & Mardiati, N. P. J. (2017). THE EFFECTS OF EARTHWORMS’ (PHERETIMA ASPERGILLUM) ETHANOL EXTRACT TOWARD THE IMPROVEMENT OF NERVE FIBERS DENSITY IN DIABETIC ULCERS CARE DEGREE II OF RATS WISTAR. MNJ (Malang Neurology Journal), 3(2), 61–72. Retrieved from https://mnj.ub.ac.id/index.php/mnj/article/view/264

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Research Article