Centella asiatica attenuates diabetes induced hippocampal changes in experimental diabetic rats.
The hippocampus is an area of the brain that is involved in short-  and long-term  memory. In rats, amnesia can be caused by hippocampal dysfunction , whereas, in higher animals including primates, memory loss could occur due to dysfunctions of both hippocampus and amygdala . The loss of neurons or axonal degeneration secondary to ischemia can result in deficits of the hippocampus-dependent spatial memory . Mild to moderate traumatic brain injury was capable of producing prolonged spatial memory deficit in rats without evidence of neuronal death . Diabetes has been linked to memory impairment in rats  and humans .On the other hand, hypoglycemia secondary to insulin overdose can also cause hippocampal injury which could result in anterograde amnesia .
Hyperglycemia could induce oxidative stress in the hippocampus  resulting in apoptosis of hippocampal synapses and neurons . Hippocampal oxidative stress is associated with increased level of lipid peroxidation products  and diminution of activity levels of endogenous antioxidant enzymes . Diabetes has been found to inhibit activity of hippocampal [Na.sup.+]-[K.sup.+]-ATPase or [Na.sup.+] pump . Diabetes has also been reported to suppress activity of [Mg.sup.2+]-ATPase  and [Ca.sup.2+]-ATPase in rat whole brain . The effect on [Mg.sup.2+]-ATPase and [Ca.sup.2+]-ATPase activity in the hippocampus of diabetic rats however remains unknown.
Centella asiatica, a herb from Mackinlayoideae family, is native to the wetlands in the tropical and subtropical regions of Asia. C. asiatica has been widely used in Ayurvedic, African, and Chinese traditional medicine . This herb was found to promote wound healing via stimulating cellular proliferation and collagen synthesis at the wound site , strengthening gastric mucosal barrier, and preventing ethanol-induced gastritis . C. asiatica has also been shown to modulate the immune system , prevent blood coagulation , act as antioxidant , prevent alleviation of oxidative stress , act as anti-inflammatory agent , and inhibit proliferation of cancer cells . Yet, the most widely reported health benefit of this herb is in improving the brain function, particularly related to memory and learning. In fact, C. asiatica has been reported to stimulate nerve regeneration in vitro  which could explain its brain protective effect. Administration of this herb to juvenile and young adult mice or rats was found to enhance their learning and memory performances [26, 27]. Meanwhile, in humans, C. asiatica has been reported to improve mental ability of the mentally retarded children  and could selectively decrease the amyloid-[beta] levels in the hippocampus .
We hypothesized that C. asiatica was effective in protecting the hippocampus against oxidative stress and inflammation caused by diabetes. This study therefore investigated the effect of C. asiatica leaves on hippocampal function as reflected by the levels of ATPases activity. Additionally, evidence of alleviation of hippocampal destruction as indicated by decreased levels of oxidative stress and inflammation and lesser signs of histopathological changes in diabetic rats was also sought.
2. Material and Methods
2.1. Chemicals. Streptozotocin (STZ) was purchased from Sigma-Aldrich Company (St. Louis, MO, USA). All other chemicals were of analytical grade.
2.2. Preparation of Leaf Aqueous Extract of C. asiatica. C. asiatica leaves were collected from Tirumala Hills, Andhra Pradesh, India. The taxonomic identification of the plant material was confirmed by the botanist at the Department of Botany, Sri Venkateswara University, Tirupati, Andhra Pradesh, India. The leaves were dried in the shade and crushed into fine powder. The aqueous extract was prepared by soaking 1kg of powder in 3L of distilled water for 48 hrs. The extracted material was filtered through Whatman number 1 (0.45 [micro]m Ref. HAWP04700, Bedford, MA, USA) filter paper. This process was repeated three or four times until the extract was rendered colorless. The extract was distilled and concentrated under reduced pressure in rotary evaporator (Rotavapor, R-210, Buchi Labortechnik, AG, Flawil, Switzerland) at 50 [+ or -] 5[degrees]C and lyophilized using freeze-dryer (Telstar, Barcelona, Spain), which yielded 7% (w/w) of freeze-dried material.
2.3. Phytochemical Screening. The freshly prepared aqueous leaf extract of C. asiatica was qualitatively tested for the presence of chemical constituents. Phytochemical screening of the extract was performed by using standard procedures  and phytochemical constituents were identified based on the characteristic color changes.
2.4. Experimental Animals. Adult male Wistar rats (12 weeks old, weighing 180 [+ or -] 10 g) were purchased from Animal House, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia. The animals were maintained under standard laboratory conditions (temperature 22 [+ or -] 1[degrees]C; 12 h light/dark cycle) and had free access to water and commercial pellet diet (Harlan diet, UK). Experimental procedures were in accordance with ARRIVE guidelines (Animals in Research: Reporting In Vivo Experiments) and European Community Guidelines/EEC Directive, 1986. This study was approved by the Animal Care and Use Committee, Faculty of Medicine, University of Malaya, with ethics number 2013-07-15/FIS/R/NS.
2.5. Acute Toxicity Studies. Acute toxicity studies were conducted according to the guidelines by the Organization for Economic Cooperation and Development (OECD, 2001). The extract was dissolved in distilled water with 1% sodium carboxymethyl cellulose (Na-CMC) at 2mL/kg and was administered to experimental animals by using oral gavage tube. Fifty male Wistar rats were divided into five groups with each group receiving a single dose of 100, 250, 500, 1000, and 2000 mg/kg b.w of C. asiatica leaf aqueous extract. Animals were continuously monitored for 4 hrs for behavioral (alertness, restlessness, irritability, vomiting, and fearfulness), neurological (spontaneous activity, convulsion, gait, bleeding orifices, and touch/pain response), and autonomic (defecation, micturition) changes. The number of demised rats in each group was recorded after 24-72 hrs. The extract was found to have no toxic effects when administered in doses up to 2000 mg/kg b.w. Hence, in this study, 100 and 200 mg/kg b.w of this extract were used in accordance with the previously reported doses which were safe .
2.6. Induction of Diabetes in Experimental Animals. Overnight-fasted adult male Wistar rats were rendered diabetic via a single intraperitoneal (i.p) injection of STZ (55 mg/kg) dissolved in 0.1 M cold citrate buffer (pH 4.5) . The rats were allowed to drink 5% glucose solution overnight to overcome drug-induced hypoglycemia. Rats in control group received citrate buffer (i.p). Fasting blood glucose (FBG) levels were measured 3 days after STZ injection and only animals with FBG levels between 300 and 400 mg/kg/day were selected for the experiment. Treatment with the extract was started on the third day following STZ injection which was considered day one. C. asiatica leaf aqueous extract was administered in a form of suspension orally by using gavage tube daily for 28 consecutive days.
2.7. Experimental Design. A total of 30 rats were used and were divided into five experimental groups of six rats per group.
Group I: normal nondiabetic rats receiving vehicle ([Na.sup.+] -CMC suspension) only.
Group II: nontreated diabetic rats receiving vehicle ([Na.sup.+] -CMC suspension) only.
Group III: diabetic rats treated with C. asiatica leaf aqueous extract at 100 mg/kg b.w.
Group IV: diabetic rats treated with C. asiatica leaf aqueous extract at 200 mg/kg b.w.
Group V: diabetic rats treated with standard antidiabetic agent (glibenclamide) at 600 [micro]g/kg b.w.
2.8. Collection of Blood and Hippocampus. 28 days after the starting of treatment, rats were weighed and overnight-fasted rats were sacrificed with i.p injection of pentobarbitone sodium (60 mg/kg b.w) anesthesia followed by cervical dislocation. Blood was collected from each rat via intracardiac puncture and allowed to clot for 30 min at room temperature. The serum was separated by centrifugation (Thermo Scientific, Model 75005286, USA) at 3000 rpm for 15 minutes. The right hippocampus was immediately harvested, washed with ice-cold saline, and weighed prior to preparation of tissue homogenate. The left hippocampus was used for histological study. The tissue somatic index was determined by the following formula:
weight of the tissue in grams/weight of body in grams x 100. (1)
2.9. Histopathological Study. The left hippocampus was fixed with 10% neutral paraformaldehyde, dehydrated through ascending concentrations of ethyl alcohol, cleared in xylene, embedded in paraffin, and then cut manually using a microtome (Histo-Line Laboratories, ARM-3600, Via Brembo, Milan, Italy) to obtain 5 [micro]m thick sections. The sections were deparaffinized and rehydrated through descending concentrations of ethyl alcohol and stained with hematoxylin and eosin (H&E). The stained tissues were dehydrated in 80% alcohol followed by 95% ethyl alcohol, placed in two changes of 100% ethyl alcohol, and cleansed with two changes of xylene. Histopathological examinations were carried out by using a phase contrast microscope with an attached camera (Nikon H600L, Tokyo, Japan).
2.10. Preparation of Tissue Homogenate. The excised right hippocampus was homogenized in ice-cold 50 mM sodium phosphate buffer (pH 7.4) containing 0.1 mM ethylenediaminetetraacetic acid (EDTA) by using a glass-teflon homogenizer (Heidolph Silent Crusher M, Germany). The supernatant was separated by means of centrifugation at 1000 xg for 20 min at 4[degrees]C and was then frozen at -80[degrees]C until use for biochemical analysis.
2.11. Determination of Lipid Peroxidation (LPO) and Antioxidant Enzyme Activities. The malondialdehyde (MDA) content, a measure of LPO, was assayed in the form of thiobarbituric acid-reactive substances (TBARS) according to the method of Esterbauer and Cheeseman . The rate of lipid peroxidation was expressed as [mu] moles of MDA formed/gram wet weight of tissue. SOD (EC 126.96.36.199) activity of the homogenates was assayed according to the method of Misra and Fridovich . The assay procedure involves inhibition of epinephrine autoxidation in alkaline medium (pH 10.2) to adrenochrome, in the presence of this enzyme. SOD activity level was expressed as the amount of enzyme that inhibits oxidation of epinephrine by 50%, which was equal to 1 U per milligram of protein. CAT (EC 188.8.131.52) activity was determined by decomposition of [H.sub.2][O.sub.2]] at 240 nm for 3 min monitored spectrophotometrically . The activity of this enzyme was expressed in [micro]mol of hydrogen peroxide ([H.sub.2][O.sub.2)]] metabolized/mg protein/min. GPx (EC 184.108.40.206) activity level was determined according to the method by Rotruck et al.  and was expressed as [micro]mol of GSH consumed/mg protein/min.
2.12. Determination of Inflammatory Markers in the Hippocampus. Tumor necrosis factor alpha (TNF-[alpha]) and interleukins (IL-1[beta], IL-6) were measured in the supernatant of homogenized hippocampal tissue by using ELISA kits (Biosource International Inc., Camarillo, CA). The procedures were carried out according to the manufacturer's guidelines. TNF-[alpha], IL-1[beta], and IL-6 were determined from a standard curve and their levels were expressed in pg/mL.
2.13. Determination of ATPase Activity Levels. [Na.sup.+]/[K.sup.+] ATPase (EC 220.127.116.11) activity was estimated in the supernatant of hippocampal tissue homogenates according to the method of Bonting . The activity of calcium-dependent ATPase ([Ca.sup.2+]-ATPase) was assayed according to the method of Hjerten and Pan . Meanwhile, the activity of magnesium-dependent ATPase ([Mg.sup.2+]-ATPase) was assayed according to the method of Ohnishi et al. . Enzymes activities were expressed in [micro]mol pi/min/mg protein. The protein concentration in hippocampal homogenate was determined according to the method of Lowry et al. .
2.14. Statistical Analyses. All data were expressed as mean [+ or -] S.D. of six determinants. Statistical significance was evaluated by one-way analysis of variance (ANOVA) using SPSS version 7.5 (SPSS, Cary, NC, USA) and individual comparisons were made by Duncan's multiple range test (DMRT).
3.1. Phytochemical Screening of Aqueous Leaf Extract of C. asiatica. Preliminary phytochemical screening revealed the presence of alkaloids, flavonoids, glycosides, saponins, terpenoids, steroids, linens, phenols, and tannins (data not shown).
3.2. Effect of Aqueous Leaf Extract of C. asiatica on FBG Levels and Tissue Somatic Index of the Hippocampus. The effects of aqueous extract of C. asiatica leaves on FBG levels at days 0 and 28 and tissue somatic index of the hippocampus in rats from the different treatment groups are shown in Table 1. In nontreated diabetic rats, the FBG levels were significantly (P < 0.001) higher than normal, nondiabetic rats. However, diabetic rats treated with 100 and 200 mg/kg of C. asiatica leaf aqueous extract showed significantly (P < 0.01) lower FBG levels on day 28 as compared to nontreated diabetic rats. In diabetic rats, hippocampal tissue somatic index was not statistically different from normal, nondiabetic rats (Table 1).
3.3. Effect of Aqueous Extract of C. asiatica Leaves on MDA and Antioxidant Enzymes Activity Levels in the Hippocampus. MDA levels were significantly (P < 0.01) higher in the hippocampal homogenates of nontreated diabetic rats as compared to normal, nondiabetic rats (Figure 1). 28-day treatment of diabetic rats with 100 and 200mg/kg b.w C. asiatica leaf aqueous extracts or glibenclamide resulted in a significantly (P < 0.01) lower MDA level in the hippocampal homogenates as compared to nontreated diabetic rats.
SOD activity was 60.93% lower in STZ-induced diabetic rats' hippocampus as compared to normal, nondiabetic rats. However, treatment of diabetic rats with 100 and 200 mg/kg b.w C. asiatica leaf aqueous extract or glibenclamide resulted in a significantly higher SOD activity in the hippocampal homogenate. CAT activity was significantly (P < 0.01) lower in nontreated diabetic rats as compared to normal, nondiabetic rats. Treatment of diabetic rats with C. asiatica leaf aqueous extract or glibenclamide resulted in a significantly higher CAT activity level as compared to nontreated diabetic rats (Figure 1). In nontreated diabetic rats, GPx activity in the hippocampus was significantly (P < 0.01) lower than that in normal, nondiabetic rats. Treatment of diabetic rats with 100 and 200 mg/kg b.w C. asiatica leaf aqueous extracts or glibenclamide resulted in a significantly higher GPx activity level in the hippocampus as compared to nontreated diabetic rats (Figure 1).
3.4. Effect of C. asiatica Leaf Extract on the Hippocampal Inflammatory Markers. The effect of C. asiatica leaf aqueous extract on inflammatory markers in the hippocampus of rats in different experimental groups is shown in Figure 2. In nontreated diabetic rats, the levels of TNF-[alpha] in the hippocampal homogenates were 252.38% higher than normal, nondiabetic rats. Diabetic rats treated with C. asiatica leaf aqueous extract at doses of 100 and 200 mg/kg b.w had a significantly lower TNF-[alpha] level in the hippocampal homogenates as compared to nontreated diabetic rats. A significantly higher IL-1[beta] (306.31%) was observed in the hippocampus of nontreated diabetic rats as compared to normal, nondiabetic rats. Treatment of diabetic rats with 100 and 200 mg/kg b.w C. asiatica leaf aqueous extract resulted in a significantly lower levels of IL-1[beta] in the hippocampus as compared to nontreated diabetic rats (P < 0.01). The hippocampal IL-6 levels were significantly higher in nontreated diabetic rats as compared to normal, nondiabetic rats (P < 0.01). Diabetic rats treated with 100 and 200 mg/kg b.w C. asiatica leaf aqueous extract had a significantly lower IL-6 level in the hippocampus as compared to nontreated diabetic rats (P < 0.01).
3.5. Effect of C. asiatica Leaf Extracts on the Hippocampal ATPase Activity Levels. Figure 3 shows the effect of C. asiatica leaf aqueous extract on ATPases activity of the hippocampus of rats in different experimental groups. The [Na.sup.+]/[K.sup.+] ATPase activity was 65.95% lower in the hippocampus of nontreated diabetic rats as compared to normal, nondiabetic rats. Treatment of diabetic rats with 100 and 200 mg/kg b.w C. asiatica leaf aqueous extract or glibenclamide resulted in a significantly higher hippocampal [Na.sup.+]/[K.sup.+]-ATPase activity as compared to nontreated diabetic rats (P < 0.01). [Mg.sup.2+]-ATPase activity was significantly lower (48.06%) in nontreated diabetic rats' hippocampus as compared to normal, nondiabetic rats. Diabetic rats treated with C. asiatica leaf aqueous extract at 100 and 200 mg/kg b.w or glibenclamide showed a significantly higher hippocampal [Mg.sup.2+]-ATPase activity as compared to nontreated diabetic rats (P < 0.01). Meanwhile, [Ca.sup.2+]-ATPase activity in the hippocampus of diabetic rats was significantly lower than normal, nondiabetic rats (P < 0.01). [Ca.sup.2+] -ATPase activity in the hippocampus of diabetic rats treated with C. asiatica leaf aqueous extract at 100 and 200 mg/kg b.w or glibenclamide was significantly higher than nontreated diabetic rats (P < 0.01).
3.6. Histopathological Changes of the Hippocampus following Treatment with C. asiatica Leaf Aqueous Extract. Figure 4 shows histological sections of the hippocampus from normal nondiabetic, nontreated diabetic, and diabetic rats treated with C. asiatica leaf extract or glibenclamide. Our findings showed that there were signs of necrosis in the subiculum, presubiculum, and cornu ammonis (CA) areas of the hippocampus of diabetic rats. Administration of C. asiatica prevented the development of necrotic changes in these areas. Higher magnification images revealed a significant decrease in the number of neurons and glial cells in the hippocampus of diabetic rats. Administration of 200 mg/kg/day b.w C. asiatica leaf extract resulted in higher hippocampal neurons and glial cells number as compared to nontreated diabetic rats.
Our findings have revealed the protective effect of C. asiatica, a herb widely consumed by Asians, against hippocampal destruction due to oxidative stress in diabetes. C. asiatica has been used in Ayurvedic medicine to improve the memory and learning abilities . Administration of this herb during postnatal period in mice has been shown to enhance learning and memory . Studies in humans have indicated that C. asiatica could improve memory in mentally retarded children . In addition, C. asiatica combined with other herbal extracts has been shown to improve memory in patients with Alzheimer's disease . These effects were attributed to the ability of this herb to preserve normal hippocampal function. We have provided evidence which showed that consumption of C. asiatica could help preserve memory function in diabetes, known to be associated with longand short-term memory impairment . Diabetes has been found to cause degenerative changes in the hippocampus  which contributed towards memory loss. Our histopathological findings including neuronal degeneration in diabetic rat hippocampus were consistent with the previous reports which indicate similar changes in the hippocampus under this condition [9, 44, 45].
Our findings showed that hippocampal ATPases activities were reduced in diabetes. Hippocampal [Na.sup.+]/[K.sup.+]-ATPase has been linked to memory function in rodents . Hippocampal neurons  and interneurons express [Na.sup.+]/[K.sup.+]-ATPase in their axonal and dendritic membranes . Insulin has been reported to stimulate activity of this pump in the rat hippocampus . In conditions associated with lack of insulin such as diabetes, hippocampal [Na.sup.+]/[K.sup.+]-ATPase activity was reduced, indicating that insulin is essential for maintaining the normal function of this pump . A marked decrease in [Na.sup.+]/[K.sup.+]-ATPase activity could adversely affect hippocampal function. Critical role of this pump in normal hippocampal function was evidence from impairment of hippocampal neuron activity in disease associated with mutation of this protein . Besides hyperglycemia, hippocampal [Na.sup.+]/[K.sup.+] ATPase activity was also inhibited by amino acids such as homocysteine  and drugs such as ouabain  and in ischaemia . In our study, the decrease in activity of this pump in diabetes could be prevented by the administration of C. asiatica leaves, suggesting ability of this herb to prevent hyperglycemia-induced inhibition on the [Na.sup.+]/[K.sup.+]-ATPase activity.
The expression of [Ca.sup.2+]-ATPase pump has been reported in rodent  and human  hippocampus. In this study, we have shown that hippocampal [Ca.sup.2+]-ATPase activity was markedly reduced in diabetes. Besides diabetes, activity of this pump was also found to be reduced in seizure . The expression of neuron-specific endoplasmic reticulum [Mg.sup.2+]-ATPase was reported in the hippocampal neurons . Our study has shown that activity of [Mg.sup.2+]-ATPase pump was reduced in diabetic condition. Treatment with C. asiatica leaf extract in diabetic rats could help preserve both [Ca.sup.2+]-and [Mg.sup.2+]-ATPases activities of the hippocampus, therefore restoring normal hippocampal function. In view that activity of all three major hippocampal ATPases was conserved, C. asiatica leaves might be useful in preserving and enhancing memory in diabetes.
We have shown that the levels of LPO product in the hippocampus of diabetic rats were increased indicating oxidative stress. Oxidative stress has been linked to neurodegeneration . Oxidative stress in the hippocampus could be increased by guanylic acid  and could be prevented by melatonin . Homocysteine was also reported to induce hippocampal oxidative stress . In diabetes, increased formation of reactive oxygen species (ROS) in the hippocampus could cause oxidative stress resulting in neuronal apoptosis . We have shown that activity of hippocampal antioxidant enzymes such as SOD, CAT, and GPx was decreased in diabetes which could contribute towards oxidative stress. A similar observation has been reported in homocystinuria where increased hippocampal oxidative stress was caused by decreased activity of endogenous antioxidant enzymes . Antioxidant enzymes help to scavenge free radicals such as nitric oxide, superoxide, and peroxides, levels of which were markedly elevated in diabetes 59]. In our study, ability of C. asiatica to reduce hippocampal oxidative stress may be attributed to the free radical scavenging effect and the ability of this herb to preserve near normal activity levels of endogenous antioxidant enzymes.
Our findings have indicated that there were signs of hippocampal inflammation in diabetic rats from the histopathological changes and elevation of inflammatory markers (IL1[beta], IL-6, and TNF-[alpha]) in hippocampal homogenates. IL-6 was reported to produce detrimental effect on the hippocampus . Higher levels of interleukins (ILs) could activate the central inflammatory mechanisms that result in hippocampal neurodegeneration leading to memory impairment. An inverse correlation between peripheral IL-6 levels and memory has been reported in human adults during the midlife period , suggesting that IL levels could affect memory. We have shown that administration of C. asiatica leaf extract resulted in the levels of hippocampal inflammatory markers in diabetic rats to be reduced to near normal, which indicates decreased hippocampal inflammation. Meanwhile, normalization of FBG levels following administration of C. asiatica leaf might also contribute to the reduction in hippocampal inflammation in diabetes.
Evidence of necrotic changes was observed in cornu ammonis (CA) and subiculum areas of the hippocampus in diabetic rats with severe loss of pyramidal neurons and glial cells (Figure 4). A previous study reported that in diabetes, neuronal degeneration was due to apoptosis . These changes were parallel with the reported decrease in hippocampal neurogenesis in mice with diabetes . Administration of C. asiatica leaf extract to diabetic rats prevented neuronal degeneration and therefore helps in maintaining normal hippocampal function in diabetes. In addition to C. asiatica, we have shown that antidiabetic drug glibenclamide could also prevent hippocampal neuronal degeneration in diabetes.
In conclusion, our study has provided mechanisms which could explain the protective role of C. asiatica leaf against hippocampal dysfunction which include preservation of near normal activity levels of the major hippocampal ATPases and the reduction in inflammatory changes and oxidative stress in the hippocampus in diabetes. Cumulatively, these effects justify the claims that C. asiatica contributes towards the preservation of memory function in diabetes.
Conflict of Interests
The authors declared that there was no conflict of interests with regard to the publication of this paper.
This study was funded by UMRG Research Grant (RG404/ 12HTM) and UMRG Internationalization Grant (RP01113HTM), University of Malaya, Kuala Lumpur, Malaysia.
 C. Piekema, R. P. C. Kessels, R. B. Mars, K. M. Petersson, and G. Fernandez, "The right hippocampus participates in shortterm memory maintenance of object-location associations," NeuroImage, vol. 33, no. 1, pp. 374-382, 2006.
 K. Henke, A. Buck, B. Weber, and H. G. Wieser, "Human hippocampus establishes associations in memory," Hippocampus, vol. 7, no. 3, pp. 249-256,1997
 B. G. Lyeth, L. W. Jenkins, R. J. Hamm et al., "Prolonged memory impairment in the absence of hippocampal cell death following traumatic brain injury in the rat," Brain Research, vol. 526, no. 2, pp. 249-258, 1990.
 M. Mishkin, "Memory in monkeys severely impaired by combined but not by separate removal of amygdala and hippocampus," Nature, vol. 273, no. 5660, pp. 297-298,1978.
 G. Biessels, A. Kamal, G. M. Ramakers et al., "Place learning and hippocampal synaptic plasticity in streptozotocin- induced diabetic rats," Diabetes, vol. 45, no. 9, pp. 1259-1266,1996.
 H. Sacai, S. Sasaki-Hamada, A. Sugiyama et al., "The impairment in spatial learning and hippocampal LTD induced through the PKA pathway in juvenile-onset diabetes rats are rescued by modulating NMDA receptor function," Neuroscience Research, vol. 81-82, pp. 55-63, 2014.
 J. R. Gravlee and J. J. Barrett, "Transient global amnesia in a collegiate baseball player with type I diabetes mellitus: a case report," Journal of Athletic Training, vol. 46, no. 3, pp. 319-321, 2011.
 A. J. Sommerfield, I. J. Deary, V McAulay, and B. M. Frier, "Short-term, delayed, and working memory are impaired during hypoglycemia in individuals with type 1 diabetes," Diabetes Care, vol. 26, no. 2, pp. 390-396, 2003.
 B. H. Lee, C. C. Lee, and S. C. Wu, "Ice plant (Mesembryanthemum crystallinum) improves hyperglycaemia and memory impairments in a Wistar rat model of streptozotocin-induced diabetes," Journal of the Science of Food and Agriculture, vol. 94, no. 11, pp. 2266-2273, 2014.
 X. Zhang, L. Xu, D. He, and S. Ling, "Endoplasmic reticulum stress-mediated hippocampal neuron apoptosis involved in diabetic cognitive impairment," BioMed Research International, vol. 2013, Article ID 924327, 9 pages, 2013.
 N. Mushtaq, R. Schmatz, L. B. Pereira et al., "Rosmarinic acid prevents lipid peroxidation and increase in acetylcholinesterase activity in brain of streptozotocin-induced diabetic rats," Cell Biochemistry and Function, vol. 32, no. 3, pp. 287-293, 2014.
 H. K. Moghaddam, T. Baluchnejadmojarad, M. Roghani et al., "Berberine ameliorate oxidative stress and astrogliosis in the hippocampus of STZ-induced diabetic rats," Molecular Neurobiology, vol. 49, no. 2, pp. 820-826, 2014.
 R. Franzon, F. Chiarani, R. H. Mendes, A. Bella-Klein, and A. T. S. Wyse, "Dietary soy prevents brain Na+, K+-ATPase reduction in streptozotocin diabetic rats," Diabetes Research and Clinical Practice, vol. 69, no. 2, pp. 107-112, 2005.
 A. Zarros, C. Liapi, P. Galanopoulou et al., "Effects of adult-onset streptozotocin-induced diabetes on the rat brain antioxidant status and the activities of acetylcholinesterase, ([Na.sup.+],[K.sup.+])and [Mg.sup.2+]-ATPase: Modulation by L-cysteine," Metabolic Brain Disease, vol. 24, no. 2, pp. 337-348, 2009.
 P Kumar, "Antidiabetic and neuroprotective effects of Trigonella foenum-graecum seed powder in diabetic rat brain," Prague Medical Report, vol. 113, no. 1, pp. 33-43, 2012.
 M.-J. R. Howes and P J. Houghton, "Plants used in Chinese and Indian traditional medicine for improvement of memory and cognitive function," Pharmacology Biochemistry and Behavior, vol. 75, no. 3, pp. 513-527, 2003.
 L. Suguna, P Sivakumar, and G. Chandrakasan, "Effects of Centella asiatica extract on dermal wound healing in rats," Indian Journal of Experimental Biology, vol. 34, no. 12, pp. 1208-1211, 1996.
 C. L. Cheng and M. W. L. Koo, "Effects of Centella asiatica on ethanol induced gastric mucosal lesions in rats," Life Sciences, vol. 67, no. 21, pp. 2647-2653, 2000.
 M. G. Jayathirtha and S. H. Mishra, "Preliminary immunomodulatory activities of methanol extracts of Eclipta alba and Centella asiatica," Phytomedicine, vol. 11, no. 4, pp. 361-365, 2004.
 T Satake, K. Kamiya, Y. An, T. Oishi, and J. Yamamoto, "The anti-thrombotic active constituents from Centella asiatica," Biological & Pharmaceutical Bulletin, vol. 30, no. 5, pp. 935-940, 2007
 M. K. Zainol, A. Abd-Hamid, S. Yusof, and R. Muse, "Antioxidative activity and total phenolic compounds of leaf, root and petiole of four accessions of Centella asiatica (L.) Urban," Food Chemistry, vol. 81, no. 4, pp. 575-581, 2003.
 M. Hussin, A. Abdul-Hamid, S. Mohamad, N. Saari, M. Ismail, andM. H. Bejo, "Protective effect of Centella asiatica extract and powder on oxidative stress in rats," Food Chemistry, vol. 100, no. 2, pp. 535-541, 2007
 M. N. Somchit, M. R. Sulaiman, A. Zuraini et al., "Antinociceptive and antiinflammatory effects of Centella asiatica," Indian Journal of Pharmacology, vol. 36, no. 6, pp. 377-380, 2004.
 T. D. Babu, G. Kuttan, and J. Padikkala, "Cytotoxic and antitumour properties of certain taxa of Umbelliferae with special reference to Centella asiatica (L.) Urban," Journal of Ethnopharmacology, vol. 48, no. 1, pp. 53-57,1995.
 A. Soumyanath, Y. Zhong, S. A. Gold et al., "Centella asiatica accelerates nerve regeneration upon oral administration and contains multiple active fractions increasing neurite elongation in-vitro," Journal of Pharmacy and Pharmacology, vol. 57, no. 9, pp. 1221-1229, 2005.
 S. B. Rao, M. Chetana, and P. Uma Devi, "Centella asiatica treatment during postnatal period enhances learning and memory in mice," Physiology and Behavior, vol. 86, no. 4, pp. 449-457, 2005.
 K. Nalini, A. R. Aroor, K. S. Karanth, and A. Rao, "Effect of Centella asiatica fresh leaf aqueous extract on learning and memory and biogenic amine turnover in albino rats," Fitoterapia, vol. 63, no. 3, pp. 231-238,1992.
 M. V. R. Appa Rao, K. Srinivasan, and T. Koteswara Rao, "The effect of Centella asiatica on the general mental ability of mentally retarded children," Indian Journal of Psychiatry, vol. 19, no. 4, pp. 54-59,1977.
 M. Dhanasekaran, L. A. Holcomb, A. R. Hitt et al., "Centella asiatica extract selectively decreases amyloid [beta] levels in hippocampus of Alzheimer's disease animal model," Phytotherapy Research, vol. 23, no. 1, pp. 14-19, 2009.
 J. B. Harborne, Phytochemical Methods, vol. 278, Springer, Berlin, Germany, 1984.
 R. Gupta and S. J. S. Flora, "Effect of Centella asiatica on arsenic induced oxidative stress and metal distribution in rats," Journal of Applied Toxicology, vol. 26, no. 3, pp. 213-222, 2006.
 G. B. Nelli, K. AS, and E. K. Kilari, "Antidiabetic effect of alpha-mangostin and its protective role in sexual dysfunction of streptozotocin induced diabetic male rats," Systems Biology in Reproductive Medicine, vol. 59, no. 6, pp. 319-328, 2013.
 H. Esterbauer and K. H. Cheeseman, "Determination of aldehydic lipid peroxidation products: malonaldehyde and 4hydroxynonenal," Methods in Enzymology, vol. 186, pp. 407-421, 1990.
 H. P. Misra and I. Fridovich, "The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase.," The Journal of Biological Chemistry, vol. 247, no. 10, pp. 3170-3175,1972.
 J. Bonaventura, W. A. Schroeder, and S. Fang, "Human erythrocyte catalase: an improved method of isolation and a reevaluation of reported properties," Archives of Biochemistry and Biophysics, vol. 150, no. 2, pp. 606-617,1972.
 J. T. Rotruck, A. L. Pope, H. E. Ganther, A. B. Swanson, D. G. Hafeman, and W. G. Hoekstra, "Selenium: biochemical role as a component of glatathione peroxidase," Science, vol. 179, no. 4073, pp. 588-590, 1973.
 S. L. Bonting, "Sodium-potassium activated adenosine triphosphatase and cation transport," Membranes and Ion Transport, vol. 1, pp. 257-363, 1970.
 S. Hjerten and H. Pan, "Purification and characterization of two forms of a low-affinity [Ca.sup.2+]-ATPase from erythrocyte membranes," Biochimica et Biophysica Acta--Biomembranes, vol. 728, no. 2, pp. 281-288, 1983.
 T Ohnishi, T Suzuki, Y. Suzuki, and K. Ozawa, "A comparative study of plasma membrane [Mg.sup.2+]-ATPase activities in normal, regenerating and malignant cells," Biochimica et Biophysica Acta, vol. 684, no. 1, pp. 67-74,1982.
 O. H. Lowry, N. J. Rosebrough, A. L. Farr, and R. J. Randall, "Protein measurement with the Folin phenol reagent," The Journal of Biological Chemistry, vol. 193, no. 1, pp. 265-275,1951.
 E. M. Williamson, Major Herbs of Ayurveda, Churchill Livingstone, Philadelphia, Pa, USA, 2002.
 M. Parle and M. Vasudevan, "Memory enhancing activity of Abana: an Indian ayurvedic poly-herbal formulation," Journal of Health Science, vol. 53, no. 1, pp. 43-52, 2007
 T. Iwai, M. Suzuki, K. Kobayashi, K. Mori, Y. Mogi, and J. Oka, "The influences of juvenile diabetes on memory and hippocampal plasticity in rats: improving effects of glucagonlike peptide-1," Neuroscience Research, vol. 64, no. 1, pp. 67-74, 2009.
 J. M. N. Duarte, R. A. Carvalho, R. A. Cunha, and R. Gruetter, "Caffeine consumption attenuates neurochemical modifications in the hippocampus of streptozotocin-induced diabetic rats," Journal of Neurochemistry, vol. 111, no. 2, pp. 368-379, 2009.
 F. E. Saravia, J. Beauquis, Y. Revsin, F. Homo-Delarche, E. R. de Kloet, and A. F. de Nicola, "Hippocampal neuropathology of diabetes mellitus is relieved by estrogen treatment," Cellular and Molecular Neurobiology, vol. 26, no. 4-6, pp. 943-957, 2006.
 S. Heo, E. Csaszar, G. Jung, T. Beuk, H. Hoger, and G. Lubec, "Hippocampal levels and activity of the sodium/potassium transporting ATPase subunit alpha-3 (AT1A3) are paralleling memory training in the multiple T-Maze in the C57BL/6J mouse," Neurochemistry International, vol. 61, no. 5, pp. 702-712, 2012.
 G. Pietrini, M. Matteoli, G. Banker, and M. J. Caplan, "Isoforms of the Na,K-ATPase are present in both axons and dendrites of hippocampal neurons in culture," Proceedings of the National Academy of Sciences of the United States of America, vol. 89, no. 18, pp. 8414-8418, 1992.
 K. S. Richards, K. Bommert, G. Szabo, and R. Miles, "Differential expression of [Na.sup.+]/[K.sup.+]-ATPase a-subunits in mouse hippocampal interneurones and pyramidal cells," The Journal of Physiology, vol. 585, part 2, pp. 491-505, 2007
 H. G. Bernstein, G. Poeggel, A. Dorn, H. Luppa, and M. Ziegler, "Insulin stimulates sodium-potassium activated ATPase from rat hippocampus," Experientia, vol. 37, no. 4, pp. 434-435,1981.
 S. F. Leong and T. K. C. Leung, "Diabetes induced by streptozotocin causes reduced Na-K ATPase in the brain," Neurochemical Research, vol. 16, no. 10, pp. 1161-1165,1991.
 S. J. Clapcote, S. Duffy, G. Xie et al., "Mutation I810N in the a3 isoform of [Na.sup.+], [K.sup.+]-ATPase causes impairments in the sodium pump and hyperexcitability in the CNS," Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 33, pp. 14085-14090, 2009.
 A. T. S. Wyse, A. I. Zugno, E. L. Streck et al., "Inhibition of [Na.sup.+],[K.sup.+]-ATpase activity in hippocampus of rats subjected to acute administration of homocysteine is prevented by vitamins E and C treatment," Neurochemical Research, vol. 27, no. 12, pp. 1685-1689, 2002.
 M. Balestrino, J. Young, and P. Aitken, "Block of ([Na.sup.+], [K.sup.+])ATPase with ouabain induces spreading depression-like depolarization in hippocampal slices," Brain Research, vol. 838, no. 1-2, pp. 37-44, 1999.
 A. T. de Souza Wyse, E. L. Streck, P. Worm, A. Wajner, F. Ritter, and C. A. Netto, "Preconditioning prevents the inhibition of [NA.sup.+],[K.sup.+]-ATPase activity after brain ischemia," Neurochemical Research, vol. 25, no. 7, pp. 971-975, 2000.
 T. J. Eakin, M. C. Antonelli, E. L. Malchiodi, D. G. Baskin, and W. L. Stahl, "Localization of the plasma membrane [Ca.sup.2+]ATPase isoform PMCA3 in rat cerebellum, choroid plexus and hippocampus," Molecular Brain Research, vol. 29, no. 1, pp. 71-80, 1995.
 D. A. Zacharias, S. J. DeMarco, and E. E. Strehler, "mRNA expression of the four isoforms of the human plasma membrane [Ca.sup.2+]-ATPase in the human hippocampus," Molecular Brain Research, vol. 45, no. 1, pp. 173-176,1997
 M. L. Garcia, K. D. Murray, V. B. Garcia, E. E. Strehler, and P. J. Isackson, "Seizure-induced alterations of plasma membrane calcium ATPase isoforms 1, 2 and 3 mRNA and protein in rat hippocampus," Molecular Brain Research, vol. 45, no. 2, pp. 230238,1997.
 J. T. Parsons, D. A. Sun, R. J. DeLorenzo, and S. B. Churn, "Neuronal-specific endoplasmic reticulum [Mg.sup.2+]/[Ca.sup.2+] ATPase [Ca.sup.2+] sequestration in mixed primary hippocampal culture homogenates," Analytical Biochemistry, vol. 330, no. 1, pp. 130-139, 2004.
 N. A. Simonian and J. T. Coyle, "Oxidative stress in neurodegenerative diseases," Annual Review of Pharmacology and Toxicology, vol. 36, no. 1, pp. 83-106,1996.
 W. M. H. Behan, M. McDonald, L. G. Darlington, and T. W. Stone, "Oxidative stress as a mechanism for quinolinic acid-induced hippocampal damage: protection by melatonin and deprenyl," British Journal of Pharmacology, vol. 128, no. 8, pp. 1754-1760, 1999.
 F. Lezoualc'h, T. Skutella, M. Widmann, and C. Behl, "Melatonin prevents oxidative stress-induced cell death in hippocampal cells," NeuroReport, vol. 7, no. 13, pp. 2071-2077,1996.
 E. L. Streck, P. S. Vieira, C. M. D. Wannmacher, C. S. DutraFilho, M. Wajner, and A. T. S. Wyse, "In vitro effect of homocysteine on some parameters of oxidative stress in rat hippocampus," Metabolic Brain Disease, vol. 18, no. 2, pp. 147-154, 2003.
 S. Pugazhenthi, A. Nesterova, P. Jambal et al., "Oxidative stress-mediated down-regulation of bcl-2 promoter in hippocampal neurons," Journal of Neurochemistry, vol. 84, no. 5, pp. 982-996, 2003.
 L. S. Rothenburg, N. Herrmann, W. Swardfager et al., "The relationship between inflammatory markers and post stroke cognitive impairment," Journal of Geriatric Psychiatry and Neurology, vol. 23, no. 3, pp. 199-205, 2010.
 A. L. Marsland, P. J. Gianaros, S. M. Abramowitch, S. B. Manuck, and A. R. Hariri, "Interleukin-6 covaries inversely with hippocampal grey matter volume in middle-aged adults," Biological Psychiatry, vol. 64, no. 6, pp. 484-490, 2008.
 Z. G. Li, W. Zhang, G. Grunberger, and A. A. F. Sima, "Hippocampal neuronal apoptosis in type 1 diabetes," Brain Research, vol. 946, no. 2, pp. 221-231, 2002.
 J. Beauquis, F. Saravia, J. Coulaud et al., "Prominently decreased hippocampal neurogenesis in a spontaneous model of type 1 diabetes, the nonobese diabetic mouse," Experimental Neurology, vol. 210, no. 2, pp. 359-367, 2008.
Nelli Giribabu, (1) Nelli Srinivasarao, (2) Somesula Swapna Rekha, (3) Sekaran Muniandy, (4) and Naguib Salleh (1)
(1) Department of Physiology, Faculty of Medicine, University of Malaya, 50603 Lembah Pantai, Kuala Lumpur, Malaysia
(2) Department of Materials Science and Engineering, National Chiao Tung University, University Road, Hsinchu 300, Taiwan
(3) Department of Zoology, Sri Venkateswara University, Tirupati, Andhra Pradesh 517502, India
(4) Department of Molecular Medicine, Faculty of Medicine, University of Malaya, 50603 Lembah Pantai, Kuala Lumpur, Malaysia
Correspondence should be addressed to Naguib Salleh; firstname.lastname@example.org
Received 9 May 2014; Accepted 1 July 2014; Published 5 August 2014
Academic Editor: Pasupuleti Visweswara Rao
TABLE 1: Effect of C. asiatica leaf aqueous extract on FBG levels and hippocampal tissue somatic index in experimental diabetic rats. Parameters Normal Diabetic 0th day blood 94.38 [+ or -] 727 438.27 * [+ or -] glucose levels 9.83 28th day blood 98.64 [+ or -] 8.67 432.16 * [+ or -] glucose levels 7.16 Hippocampal tissue 0.04 [+ or -] 0.01 [0.04.sup.ns] [+ or -] somatic index 0.01 Diabetic Parameters 100 mg/kg b.w 200 mg/kg b.w C. asiatica C. asiatica 0th day blood [436.81.sup.ns] [437.68.sup.ns] glucose levels [+ or -] [+ or -] 7.69 9.63 28th day blood 21737* [+ or -] 203.44* [+ or -] glucose levels 8.36 8.42 Hippocampal tissue [0.04.sup.ns] [0.04.sup.ns] somatic index [+ or -] [+ or -] 0.01 0.01 Parameters 600 [micro]g/kgb.w glibenclamide 0th day blood [436.65.sup.ns] glucose levels [+ or -] 9.76 28th day blood 182.16 * [+ or -] glucose levels 8.71 Hippocampal tissue [0.04.sup.ns] somatic index [+ or -] 0.01 Value represents means [+ or -] S.D. for 6 rats per group. *P < 0.01 as compared to normal, nondiabetic rats group; ([dagger]) P < 0.01 as compared to nontreated diabetic rats.
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|Title Annotation:||Research Article|
|Author:||Giribabu, Nelli; Srinivasarao, Nelli; Rekha, Somesula Swapna; Muniandy, Sekaran; Salleh, Naguib|
|Publication:||Evidence - Based Complementary and Alternative Medicine|
|Date:||Jan 1, 2014|
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