Chronic garlic administration protects rat heart against oxidative stress induced by ischemic reperfusion injury
© Banerjee et al; licensee BioMed Central Ltd. 2002
Received: 25 May 2002
Accepted: 16 August 2002
Published: 16 August 2002
Oxidative stress plays a major role in the biochemical and pathological changes associated with myocardial ischemic-reperfusion injury (IRI). The need to identify agents with a potential for preventing such damage has assumed great importance. Chronic oral administration of raw garlic has been previously reported to augment myocardial endogenous antioxidants. In the present study, the effect of chronic oral administration of raw garlic homogenate on oxidative stress induced by ischemic-reperfusion injury in isolated rat heart was investigated.
Raw garlic homogenate (125, 250 and 500 mg/kg once daily for 30 days) was administered orally in Wistar albino rats. Thereafter, hearts were isolated and subjected to IRI (9 min. of global ischemia, followed by 12 min of reperfusion; perfusion with K-H buffer solution; 37°C, 60 mm Hg.). Significant myocyte injury and rise in myocardial TBARS along with reduction in myocardial SOD, catalase, GSH and GPx were observed following IRI. Depletion of myocardial endogenous antioxidants and rise in TBARS were significantly less in the garlic-treated rat hearts. Oxidative stress induced cellular damage as indicated by ultrastructural changes, like disruption of myofilament, Z-band architecture along with mitochondrial changes were significantly less.
The study strongly suggests that chronic garlic administration prevents oxidative stress and associated ultrastructural changes, induced by myocardial ischemic-reperfusion injury.
Oxidative stress is a well established etiopathogenic factor of ischemic heart disease (IHD) and its consequences. Reperfusion of the ischemic myocardium is the only logical approach for the successful management of patients with acute obstruction of coronary arteries. Morphologic observations of the ischemic myocardial tissue undergoing reperfusion suggest that reperfusion injury is a true pathologic phenomenon and a distinct entity from the preceding ischemic injury. Generation of reactive oxygen species immediately upon reperfusion has been documented in experimental conditions, as well as in patients with acute myocardial infarction undergoing thrombolysis, coronary angioplasty or open heart surgery . Upon reperfusion, molecular oxygen undergoes sequential reduction to form reactive oxygen species, including superoxide anion and hydroxyl radical, in addition to hydrogen peroxide. The interaction of oxygen-derived free radicals with cell membrane lipids and essential proteins contribute to myocardial cell damage, leading to depressed cardiac function and irreversible tissue injury with concomitant depletion of certain key endogenous antioxidant compounds, e.g., superoxide dismutase (SOD), catalase, reduced glutathione (GSH) and glutathione peroxidase (GPx) .
Although antioxidant administration during reperfusion injury has been shown to reduce the severity of the ischemic reperfusion injury, yet some properties of antioxidants such as cytotoxicity , pro-oxidant activity  or high molecular weight in case of SOD, limited their therapeutic application. Use of plant extracts , food supplement  and even drugs  which augment major cellular endogenous antioxidants following chronic administration have been identified as a promising therapeutic approach to combat oxidative stress associated with ischemic heart disease. The property of augmenting cellular endogenous antioxidants has been defined as a major constituent of myocardial adaptation against oxidative stress .
Both epidemiological and experimental studies have claimed that garlic (Allium sativum) has significant beneficial effects in ischemic heart disease (IHD) [9, 10]. Garlic reduces a multitude of risk factors which play a decisive role in the genesis and progression of IHD, e.g., hypolipidemic effect, lowering of arterial blood pressure and inhibition of platelet aggregation . Recently, it has been shown that chronic administration of garlic augmented SOD and catalase in rat heart . In view of this observation, the present study was designed to investigate whether this property of garlic could offer protection against oxidative stress arising out of ischemic-reperfusion injury in isolated rat heart.
Effect of chronic administration of raw garlic homogenate on body weight gain in one month
gm/ 100 gm rat
14.44 ± 1.89
Garlic 125 mg/kg (G-125)
13.75 ± 1.37
Garlic 250 mg/kg (G-250)
16.94 ± 1.48
Garlic 500 mg/kg (G-500)
13.97 ± 1.25
Effect of chronic administration of raw garlic homogenate on TBA-RS, GSH, catalase, SOD and GPx in rat heart after ischemic-reperfusion injury
TBA-RS (n mole/gm wet wt.)
GSH (μg/gm wet wt.)
CATALASE (U/mg protein)
SOD (U/mg protein)
GPx (mU/mg protein)
203.03 ± 11.52
479.17 ± 40.76
49.49 ± 2.91
6.88 ± 0.79
357.41 ± 38.41
259.96 ± 22.48ac
284.57 ± 24.33cc
14.41 ± 1.94cc
4.61 ± 0.65ac
272.30 ± 24.02ac
161.43 ± 26.05b
366.93 ± 18.44b
21.01 ± 5.56
16.29 ± 3.16c
287.83 ± 37.29
130.78 ± 11.36c
398.19 ± 13.90b
45.35 ± 5.69c
17.99 ± 2.93c
316.20 ± 51.26
197.77 ± 25.79a
371.18 ± 16.53b
12.35 ± 1.70
4.23 ± 0.59
288.31 ± 28.92
There was significant (p < 0.05) increase in myocardial TBARS in the group C-IR when compared to the control (C). Significant decrease in the level of myocardial TBARS was observed in groups 1, G-125 (p < 0.02), G-250 (p < 0.001) and G-500 in comparison to the C-IR group.
In C-IR group, there was a significant (p < 0.05) reduction in myocardial SOD activity when compared to control (C) group. Significant (p < 0.001) increase in myocardial SOD activities was observed in groups G-125 and G-250 but not in group G-500 when compared to C-IR.
In the C-IR group there was a significant (p < 0.001) decrease in myocardial catalase activity compared to control (C). In the groups G-125 and G-500, there was no significant increase in the level of myocardial catalase activities compared to C-IR. However, significant (p < 0.001) increase in myocardial catalase activity was seen only in group G-250.
Significant (p < 0.001) decrease in myocardial GSH level was observed in the group C-IR in comparison to the control (C). In the groups G-125, G-250 and G-500, there was an significant (p < 0.02) increase of myocardial GSH levels when compared to C-IR.
Significant (p < 0.05) reduction in GPx activity was observed in C-IR group. No change of GPx activity was observed in any of the garlic fed groups when compared to C-IR group.
Light microscopic changes
Ultrastructural changes (transmission electron microscopy)
In the present study, ischemic reperfusion injury (IRI) was associated with increased oxidative stress, as evidenced by increase in myocardial TBARS and depletion of myocardial endogenous antioxidants such as SOD, catalase, GSH and GPx. Similar observations were made earlier by different other studies, using similar models [13, 19–21]. Ultrastructural changes, like disruption of myofilaments and Z-band architecture along with mitochondrial swelling also occurred in the myocytes following ischemia reperfusion. Increased oxidative stress might be responsible for such myocyte injuries. Chronic garlic administration prevented the oxidative stress and the ultrastructural changes associated with IRI. The mechanism of such protection of chronic garlic administration may be postulated in the light of the phenomenon of myocardial adaptation.
Myocardial adaptation against oxidative stress is mediated through augmentation of a number of cellular antioxidants, such as SOD, catalase, glutathione peroxidase, glutathione [8, 22–24]. As IRI is a common sequel of ischemic heart disease (IHD) and oxidative stress plays a central role in its etiopathogenesis, protection against oxidative stress through a novel mechanism like myocardial adaptation holds promise as an effective therapeutic approach. Myocardial adaptation occurs in response to various kinds of obnoxious stimuli, like ischemia , certain endotoxins , reactive oxygen species , etc. and protects heart from subsequent exposure to injuries of similar or more severe nature [28, 29]. Although protective in nature, the basic mechanisms of such induction of adaptation are harmful in themselves and, therefore, cannot be relied upon as acceptable therapeutic methods. Therefore, pharmacological [30, 31], as well as transgenic approaches [32, 33] of myocardial adaptation has recently become the focus of recent scientific interest.
It is interesting to note that different plants and plant extracts can also stimulate the synthesis of cellular antioxidants [5, 34–36]. It was reported earlier that aged garlic extract increases the level of SOD, GSH and GPx in vascular endothelial cell [37, 38] and inhibits oxidative-stress mediated ischemic-reperfusion damage in rat brain . We have also reported that chronic oral administration of raw garlic homogenate caused a significant increase in basal SOD and catalase activities of rat heart, which was associated with a concomitant decrease in basal lipid peroxidation . Simultaneous increase in SOD and catalase activities, as observed with chronic administration of garlic homogenate has special importance of being more beneficial than increase in SOD activity alone, because without a concomitant increase in catalase activity, increased SOD activity may lead to intracellular accumulation of H2O2 with detrimental effects.
Protection against ischemia reperfusion induced oxidative stress in garlic treated rat hearts was evidenced by preservation of endogenous antioxidants and prevention in rise of TBARS. Among the three garlic treated groups, only 250 mg/kg group showed the best protection in terms of biochemical and histopathological evidences. Garlic in 125 mg/kg group did not show better histopathological improvement compared to garlic 500 mg/kg group. This can be explained by our previous study  where only 250 and 500 mg/kg doses of chronic garlic administration augmented both SOD and catalase activities, while 125 mg/kg garlic administration augment only SOD activity.
The observations made in the present study showed for the first time that chronic garlic administration prevents oxidative stress and associated ultrastructural changes induced by myocardial ischemic reperfusion injury.
Garlic (Allium sativum) bulbs were purchased from a local market. The cloves were peeled, sliced, ground into a paste and a homogenate was made in distilled water. Three different concentrations of the extract were prepared, 0.05, 0.1 and 0.2 gm/ml, corresponding to 125 mg, 250 mg and 500 mg/kg body weight of animal. Oral feeding was done within 30 minutes of the preparation of homogenate.
The study was approved by the Institute Animal Care Ethics Committee. Laboratory bred Wistar albino rats of both sexes weighing between 150 and 200 gm, maintained under standard laboratory conditions at 25 ± 2°C, relative humidity 50 ± 15% and normal photo period (12 hr dark/12 hr light) were used for the experiment. Commercial pellet diet and water were provided ad libitum. Commercial pellet diet (Ashirwad, India) contains protein: 24%, fat: 5%, fiber: 4%, carbohydrate: 55%, calcium: 0.6%, phosphorous: 0.3%, moisture: 10% and ash: 9% w/w.
All chemicals were of analytical grade and chemicals required for sensitive biochemical assays were obtained from Sigma Chemicals, St Louis, USA. Double distilled water was used in all biochemical assays.
Rats were randomly divided into four groups, each group having 6 rats. Aqueous homogenate of garlic bulb was fed by oral gavage everyday at a fixed time (10.00 a.m) for 30 days in three different doses. Control rats were fed normal saline daily for 30 days. Changes in body weight, food and water intake patterns of rats in all groups were noted throughout the experimental period. After 48 hours of the last dose, rats were heparinised [375 units/200 gms i.p], anaesthetized after 30 min. with sodium pentobarbitone (60 mg/kg i.p) and subjected to the following protocol.
Production of ischemic-reperfusion injury in isolated rat heart
Hearts were rapidly excised and washed in ice-cold saline, and then perfused with the non-recirculating Langendorff's technique (Hufesco, Hungary), in constant pressure mode with modified Kreb's Henseleits buffer  containing [in mM]: glucose 11.1; NaCl 118.5; NaHCO3 25; KCl 2.8; KH2PO4 1.2; CaCl2 1.2; MgSO4 0.6, with a pH of 7.4. The buffer solution equilibrated with 95% O2 + 5% CO2 was delivered to the aortic cannula at 37°C under 60 mm Hg pressure. Following 5 min-equilibration period, hearts were subjected to 9 min. of zero-flow [ischemia] and 12 min of re-flow [reperfusion] (IR injury).
Group C: Normal saline-fed rat hearts subjected to 26-min. perfusion.
Group C-IR: Normal saline-fed rat hearts subjected to IR injury.
Group G-125: 125 mg/kg/day for 30 days of garlic homogenate fed rat hearts subjected to IR injury.
Group G-250: 250 mg/kg/day for 30 days of garlic homogenate fed rat hearts subjected to IR injury.
Group G-500: 500 mg/kg/day for 30 days of garlic homogenate fed rat hearts subjected to IR injury.
At the end of each experiment, myocardial tissue was stored in liquid nitrogen for biochemical estimations, 10% buffered formalin for light microscopic studies and Karnovsky fixative for electron microscopic studies.
Thiobarbituric acid reactive substances (TBARS)  was measured as a marker of lipid peroxidation and endogenous antioxidants, e.g., superoxide dismutase (SOD) , catalase , reduced glutathione (GSH)  & glutathione peroxidase (GPx)  were estimated.
a) Light microscopic study
Myocardial tissue was fixed in 10% formalin, routinely processed and embedded in paraffin. Paraffin sections (3 μm) were cut on glass slides and stained with hematoxylin and eosin (H&E), periodic acid Schiff (PAS) reagent and examined under a light microscope.
b) Ultrastructural study (transmission electron microscopy)
Small pieces of myocardial tissue were washed in cold 0.1 M phosphate buffer after fixation (Karnovsky fixative) and post-fixed for two hours in 1% osmium tetraoxide in the same buffer at 4°C. After several washes in 0.1 M phosphate buffer, the specimens were dehydrated using graded acetone solutions and embedded in CY 212 araldite. Ultrathin sectioning (80–100 nm) of the tissue blocks was carried out using an ultracut E (Reichert, Austria) microtome. The sections were stained in alcohol uranyl acetate and lead citrate and viewed under a transmission electron microscope (Philips CM 10) operated at 60 KV.
All values are expressed as mean ± SE. One way ANOVA was applied to test for significance of biochemical data of the different groups. Significance is set at p < 0.05.
The authors acknowledge the financial support from Council of Scientific and Industrial Research (CSIR), Government of India, New Delhi, India, (9/6 177/99-EMR-I) for this work.
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