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Abstract and References |
Transactions on Science and Technology Vol. 4, No. 3-3, 372 - 383, 2017 |
An Evaluation of Antioxidant and Antidiabetic Potential of Cynometra cauliflora (Nam-nam, Fabaceae) |
Azalina Farina Abd Aziz, Md. Safiul Alam Bhuiyan, Mohammad Iqbal |
ABSTRACT Oxidative damage of biomolecules is implicated in the pathogenesis of various chronic diseases including diabetes. This has led to intensive investigation aimed at reducing the extent of such oxidative injury. Cynometra cauliflora or normally known as “Nam-nam” is a native of Malaysia, grown mainly in northern peninsular Malaysia and possesses many medicinal values in treating several diseases and for health care maintenance. However, antidiabetic and antioxidative potential of C. cauliflora have not been fully investigated. Therefore, the present study was aimed to evaluate the antioxidative, hypolipidemic and hypoglycemic potentials of C. Cauliflora extract against alloxan induced diabetes rats. Treatment of rats with alloxan resulted in a significant increase (P<0.05) level of blood glucose, total cholesterol and low density lipoprotein. On the other hand, oxidative stress was noticed in pancreatic tissue as evidenced by a significant decrease in glutathione level, catalase activity, and also significant increase in malondialdehyde when compared to normal saline control group. Pancreases were examined by hematoxylin and eosin staining. Additionally, serum biochemistry and oxidative stress markers were consistent with the pancreatic histopathological studies. Treatment of diabetic rats with C. Cauliflora extract significantly prevented these alterations and attenuated alloxan-induced oxidative stress. The results of the present study indicated that the hypolipidemic and hypoglycemic potentials of C. Cauliflora might be ascribable to its antioxidant and free radical scavenging properties. Thus, it concluded that C. Cauliflora may be helpful in the prevention of diabetic complications associated with oxidative stress. KEYWORDS: Cynometra cauliflora; Nam-nam; Antidiabetic; Antioxidant activity; Oxidative stress Download Full Text PDF |
REFERENCES
Alkhamees, O. A. (2013). Morin a flavonoid
exerts antioxidant potential in
streptozotocin-induced hepatotoxicity.
British
Journal of Pharmacology and Toxicology, 4(1),
10-17.
Ayala, A., Muñoz, M. F. & Argüelles, S. (2014).
Lipid peroxidation: production, metabolism, and
signaling mechanisms of malondialdehyde and
4-hydroxy-2-nonenal.
Oxidative
Medicine And Cellular Longevity, 2014,
1-31
Buege, J. A. & Aust, S. D. (1978). Microsomal
lipid peroxidation.In Fleischer, S. and Packer,
L. (eds.).
Methods in Enzymology, 52, 302-310.
Claiborne, A. L. (1985). Catalase activity. CRC
handbook of methods for oxygen radical research,
1: 283-284.
Das, P. C., Mostofa, M., Sarkar, A. K., & Ali,
M. (2008). Comparative efficacy of two medicinal
plants and Amaryl® tablet (Glimepiride) in
induced diabetes mellitus in rat.
Journal of
the Bangladesh Agricultural University, 6(2),
297-300.
El-Demerdash, F. M., Yousef, M. I., & El-Naga,
N. A. (2005). Biochemical study on the
hypoglycemic effects of onion and garlic in
alloxan-induced diabetic rats.
Food and
Chemical Toxicology, 43(1), 57-63.
Hsueh, C. J., Wang, J. H., Dai, L., & Liu, C. C.
(2011). Determination of alanine
aminotransferase with an electrochemical nano
Ir-C biosensor for the screening of liver
diseases.
Biosensors, 1(3), 107-117.
Huang, H. C., Lien, H. M., Ke, H. J., Chang, L.
L., Chen, C. C., & Chang, T. M. (2012).
Antioxidative characteristics of anisomeles
indica extract and inhibitory effect of
ovatodiolide on melanogenesis.
International journal of molecular sciences,
13(5), 6220-6235.
Ikram, E. H. K., Eng, K. H., Jalil, A. M. M.,
Ismail, A., Idris, S., Azlan, A., & Mokhtar, R.
A.M. (2009). Antioxidant capacity and total
phenolic content of Malaysian underutilized
fruits.
Journal of Food Composition and Analysis,
22(5), 388-393.
Indradevi, S., Ilavenil, S., Kaleeswaran, B.,
Srigopalram, S., & Ravikumar, S. (2012).
Ethanolic extract of Crinum asiaticum attenuates
hyperglycemia-mediated oxidative stress and
protects hepatocytes in alloxan induced
experimental diabetic rats.
Journal of
King Saud University-Science, 24(2),
171-177.
Jollow, D. J., Thorgeirsson, S. S., Potter, W.
Z., Hashimoto, M., & Mitchell, J. R. (1974).
Acetaminophen-induced hepatic necrosis.II. Role
of covalent binding in vivo.
Journal of
Pharmacology and Experimental Therapeutics,
187, 195-202.
Koh, P. H. (2011).
Chemopreventive effects of selected herbal
plants against carbon tetrachloride-mediated
oxidative tissue damage in rats (Doctoral
dissertation, Universiti Malaysia Sabah).
Makinwa, T. T., Adiele, H., Oyebiyi, O. O.,
Alabi, T. D., & Sodeinde, K. O. (2013), Effects
of NaCl and Lime water on the Hypoglycemic and
Antioxidant activities of Ocimum gratissimum in
Alloxan-induced Diabetic rats.
IOSR Journal of Pharmacy and biological Sciences, 8(3), 1-5
Marnett, L. J. (1999). Lipid peroxidation—DNA
damage by malondialdehyde.
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis,
424(1), 83-95.
Mudiana, D. & Darmayanti, A. S. (2010)
Perkecambahan Cynometra cauliflora Linn.
Navarro, M. C., MONTIALLA, M., Martín, A.,
Jiménez, J., & Utrilla, M. P. (1993). Free
radical scavenger and antihepatotoxic activity
of Rosmarinus tomentosus.
Plant
medical, 59(4), 312-314.
Ndiaye, M., Diatta, W., Sy, A. N., Dièye, A. M.,
Faye, B., & Bassène, E. (2008). Antidiabetic
properties of aqueous barks extract of Parinari
excelsa in alloxan-induced diabetic rats.
Fitoterapia, 79(4), 267-270.
Pushparaj, P. N. (2004).
Evaluation
of the anti-diabetic properties of Averrhoa
bilimbi in animals with experimental diabetes
mellitus (Doctoral dissertation), National
University of Singapore.
Rajasekaran, S., Sivagnanam, K., & Subramanian,
S. (2005). Antioxidant effect of Aloe vera gel
extract in streptozotocin-induced diabetes in
rats. Pharmacology Reports, 57(1), 90-6.
Ramesh, B., & Saralakumari, D. (2012).
Antihyperglycemic, hypolipidemic and antioxidant
activities of ethanolic extract of Commiphora
mukul gum resin in fructose-fed male Wistar
rats.
Journal of Physiology and Biochemistry,
68(4), 573-582.
Rehab Ahmed, R. (2012). Effect of quercetin on
the endocrine pancreas of the experimentally
induced diabetes in male albino rats: a
histological and immunohistochemical study.
Journal of
Diabetes & Metabolism,
3(3),
1000182
Sözmen, E. Y., Sözmen, B., Girgin, F. K., Delen,
Y., Azarsiz, E., Erdener, D., & Ersöz, B.
(2001). Antioxidant enzymes and paraoxonase show
a co-activity in preserving low-density
lipoprotein from oxidation.
Clinical
and Experimental Medicine, 1(4),
195-199.
Swathi, P., Kumar, K. E., & Kumar, T. J. (2014)
Effect of methonolic fruit pericarp extract of
garciniaindicaonhypercholestremic of diabetic
rats induced with alloxane.
International Journal Pharmaceutical, Chemistry
and Biology Science, 4(4), 994-1001
Varvařovská, J., Racek, J., Štětina, R., Sýkora,
J., Pomahačová, R., Rušavý, Z.,& Stožický, F.
(2004). Aspects of oxidative stress in children
with type 1 diabetes mellitus.
Biomedicine and Pharmacotherapy, 58(10),
539-545.
Zanariah, H., Chandran, L. R., Mohamad, W. B.,
Wan Nazaimoon, W. M., Letchuman, G. R.,
Jamaiyah, H., Fatanah, I., Nurain, M. N., Helen
Tee, G. H. & Rodi, I. M. (2008). DWP1-3
Prevalence of diabetes mellitus in Malaysia in
2006—Results of the 3rd National Health and
Morbidity Survey (NHMS III).
Diabetes Research and Clinical Practice,
79(1), S21.
Zhang, H., & Brunk, U. (1995). Insulinoma cells
in culture show pronounced sensitivity to
alloxan-induced oxidative stress.
Diabetologia, 38(6), 635-641. |