Study Design and Period
An experimental study was conducted at animal laboratory of Biochemistry Department, College of Health Sciences, Addis Ababa University, Etiopia from December 2018 to May 2019 to investigate the antidiabetic effect of Persea americana fruit pulp juice in male albino Wistar rats.
Ethical Consideration
The study was conducted after the proposal was evaluated and approved by Department of Biochemistry Research and Ethical Review Committee (DRERC) by protocol no. M.Sc.13/17. All experimental activities conducted in the laboratory was in accordance to ethical declaration of national and international standards for experimental animals, which protect the right of experimental animal and minimize suffer, hunger, pain, thirst, injury, discomfort and fear to the best minimal level.
Sample Size Determination
An appropriate sample size determination is important since too small size misses the real effect in an experiment while a sample size larger than necessary will lead to wasting resources and ethical issues on sacrificed animals (24). Number of animals was calculated according to Federer rule :(k-1) (n-1) ≥15 where k, is the number of groups and n, number of subjects per group; and drop-out size (do) was estimated 10%, the minimal size of sample was determined as: ndo= 5/(1-do)2 = 5/(1-0.1)2 = 5/0.81 = 6.2≈6 where ndo is minimal sample size (25). The size of sample in each group was at 6 rats. The study was conducted on six groups, so the total sample size was 6 groups × 6 rats = 36 rats.
Experimental Animals and Study Protocol
Male albino Wistar rats (4-5 weeks) weighing 150-200 g were obtained from Department of Pharmacology, College of Health Sciences, Addis Ababa University. The animals were housed in polypropylene plastic cages and maintained under standard laboratory conditions of room/optimum temperature and 12 hour light/dark cycle at Biochemistry animal laboratory and fed on a standard commercial rat pellet and water ad libitum. At 9 - 10 weeks of age, the rats were randomly assigned into six groups. Throughout the experiment, each rat in the assigned group was identified by giving a specific number on its tail by permanent marker. The allocation and treatment of the rats were as follows:
Group I: Normal control rats injected citrate buffer and administered 3.5 ml/Kg of distilled water orally
Group II: HFD and STZ induced diabetic rats that served as diabetic control and were given distilled water daily.
Group III: HFD and STZ induced diabetic rats treated with 7 mg/Kg of metformin orally
Group IV: HFD and STZ induced diabetic rats treated with 632 mg/Kg of Persea americana fruit juice.
Group V: HFD and STZ induced diabetic rats treated with 1264 mg/Kg of
Persea Americana fruit juice.
Group VI: HFD and STZ induced diabetic rats treated with 1896 mg/Kg-BW/day of Persea Americana fruit juice.
High Fat Diet (HFD) Preparation
Many experiments have used rats fed with commercial lard (animal fat) as an obesity model (26). However, since commercial lard is not available in Ethiopia, the HFD used in this experiment was prepared from locally available bovine fat. To prepare the HFD, 40% purified fat was mixed with 60% of pellet (40%/60% w/w). Since the standard pellet powder consists of 20% fat, 60% carbohydrate and 20% protein (27), the final percentage of fat is 52% (i.e., 52%/100% W/W). Hence, the term, ‘high fat diet’ used in this study refers to a diet containing 52% fat, 36% carbohydrate and 12% of protein.
Induction of Type 2 Diabetes Mellitus
There are different methods to induce diabetes mellitus in animal model (28). In our study, high fat diet (HFD) and low dose streptozotocin (STZ) induced diabetic rat model was used. This model involves a combination of a high fat diet to bring about hyperinsulinemia, insulin resistance and glucose intolerance followed by treatment with the β cell toxin STZ, which results in a severe reduction in functional β cell mass. These two stressors were designed to induce the features of human T2DM pathology to the rats within a shorter period of time scale.
Streptozotocin Injection
After 4 weeks of dietary manipulation, the rats were fasted overnight and injected intraperitoneally with freshly prepared STZ at a concentration of 35 mg/Kg body weight in 0.1M citrate buffer (pH = 4.5). The rats were given 5% glucose solution from 4 to 8 hours to reduce STZ induced hypoglycemia (29), and fasting blood glucose was determined after 72hrs by glucometer. The rats with blood glucose level above 200 mg/dL were considered as diabetic and those with normal blood glucose level were re-injected STZ to induce T2DM.
Preparation of Persea americana Fruit Juice and Dosage Calculation
Persea americana mill fruit was purchased from Jimma town, 350 Km South West of Addis Ababa, Ethiopia and identified by taxonomists in national herbarium, Addis Ababa University. The ripen fruit was washed carefully with distilled water and cut off by spoon, peeled off and the seed removed. Then the edible part of fruit was mixed by blender to prepare a juice as consumed by humans. In our study, Persea americana juice was used to treat diabetic induced male albino Wistar rats. The juice was prepared by adding water to 80gm of wet fruit pulp up to 200ml mark. Then the juice was dried to know the weight of the fruit powder that is found in juice. The dry mass of the fruit in 200ml juice was found to be 44.5gm. The volume of juice given to rats was also extrapolated from volume of human daily consumption, which is (200ml of juice /day in 70Kg). In this study the average body weight (BW) of rats were 250gm. Therefore, the volume of juice given to rats was 0.71ml. The approximate amount of Persea americana fruit pulp powder in 0.71ml of juice is approximately158mg. Accordingly, 158mg, 316mg and 474mg /250gm BW/day was considered as a low, moderate and high dose of Persea americana fruit pulp juice, respectively. Similarly, 0.7, 1.4 and 2.1ml/250gm BW/day were considered as low, moderate and higher volume that is given to rats daily. The doses (158mg, 316mg and 474mg /250gm BW/day) were converted to standard unit (mg/Kg) as 632, 1264, and 1896mg/Kg/day, respectively and used in this thesis document. The Persea Americana fruit juice was administered for six weeks orally from 9:30-10:30 AM.
Extrapolation of Metformin Dose
Safe and effective drug dosing is necessary regardless of its purpose of administration. There are several instances where in the initial dose of a particular drug is unavailable in a specific species. Therefore, choosing starting dose of such drugs for research, experiments, or clinical trials in animals and humans is a concern. The human dose of metformin drug was extrapolated to animal dose as follows (30).
Blood Sample Collection, Serum Preparation and Storage
At the end of the experiment, the rats were fasted overnight and euthanized by anesthetizing with diethyl ether and then blood was collected by direct cardiac puncture to serum separator tube. Then, the blood was left at room temperature for 30 minutes to coagulate and centrifuged at 3000 rpm for 10 minutes. The serum sample was transferred to necked tube and stored in deep freezer at -80 °C until the biochemical analyses were done.
Biochemical Tests
Total cholesterol (TC), triglyceride (TG), high density lipoprotein cholesterol (HDL-C), total protein (TP) and creatinine were determined with chemistry analyzer. Low density lipoprotein cholesterol (LDL-C) level was calculated using Frieldwald’s formulae (31). Overnight fasting blood glucose was collected from the tail of the rats, and measured with One Touch GlucoSure on 0, 14th, 28th and 42th days of the experiment.
Statistical Data Analysis
The statistical data were analyzed using SPSS version 22. 00. The results of food consumption, body weight and biochemical parameters were expressed as mean ± SEM. The statistical differences between the means were examined using analysis of variance (ANOVA) followed by Post Hoc Tukey’s multiple comparisons. The p-values < 0.05 were declared as statistically significant.