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International Journal of Herbs, Spices and Medicinal Plants IJHSMP

Vol. 3(1), pp. 025-030, May, 2018. © www.premierpublishers.org, ISSN: 2123-7362

Research Article

Pharmacodynamics Study on the Effect of Jerusalem


artichoke Compound Granule Particles on type II diabetic
mice
Meiyu Cui1, Miaomiao Lin2, Danna Lu3, Sitan Chen4, Mingqi Niu5, Bo Zhao6, Zejia Zhang7,
Guowei Zhang8*
1,2,3,4,5,6,7,8
College of Chinese Medicine, Hebei University, Baoding, 071000, Hebei province, China.

The experiment was performed to study the therapeutic effect of Jerusalem artichoke compound
granule particles on streptozotocin-induced type II diabetic model mice. Specific Pathogen Free
(SPF) male mice with Streptozotocin (STZ) 120 mg. Kg -1 were given intraperitoneal injection
disposably to establish type II diabetic mice model; Experimental animals were divided into 5
groups. Among them, the blank group and the model control group were both given distilled water,
the positive dose group was given glyburide, the high-dose group, the middle-dose group and the
low-dose group were respectively given Jerusalem artichoke compound particles 3000, 1500 and
750 mg/kg-1. Each mouse was given 2mL/100g corresponding drugs. After 4 weeks, fasting blood
glucose (FBG) was measured with glucose meter, total superoxide disambiguation (SOD) and
malonic acid (MDA) content in serum were also measured with kits. Following 3000, 1500 and 750
mg/kg-1 Jerusalem artichoke particles treatment for 4 weeks, blood glucose concentrations were
decreased by 16.82%, 36.89% and 23.90% in type II diabetic mice respectively. Compared with the
model control group, SOD concentrations were increased by 10.01%, 33.28%, 19.51%, and MDA
concentrations were decreased by 58.29%, 64.45%, 59.94%. Jerusalem artichoke compound
granule particles have a hypoglycemic effect on type II diabetic rats.

Keywords: Jerusalem artichoke compound granule particles; Type II diabetes mellitus; Blood glucose; Total superoxide
disambiguation in serum; Total malonic acid in serum

INTRODUCTION
Type 2 diabetes mellitus, also known as non-insulin view of the compound to further explore the curative effect
dependent diabetes mellitus (NIDDM), is a kind of of Jerusalem artichoke compound in lowering blood sugar
heterogeneity disease, which is mainly manifested sulin and mechanism of action, and to optimize the preparation
resistance with relatively insufficient sulin and insulin process.
deficiency with insulin resistance. It is also the most
common type of diabetes, for which insulin injection has no
effect and it can only be controlled by proper diet treatment
(Vandam RB et al., 2002). At the same time, some new
resource food and healthy food supplements are used to
help alleviate the symptoms and discomforts caused by
*Corresponding author: Guowei Zhang, Department of Chinese
diabetes (Hong Yin et al., 2008). The study has shown that Medicine, Hebei University, China No.342 Yuhua Road, Baoding, China.
the Jerusalem artichoke particles have a significant effect Tel.: +86 13663125198. E-mail: xxzgw@163.com Co-Author Email:
on the treatment of type I and type II diabetic rats (Bo Zhao 1
1378716379@qq.cm, Tel.: +8618831293920; 2840368667@qq.cm; Tel.:
et al., 2017). In clinical application, Jerusalem artichoke +8613933223924; 32867352796@qq.cm, Tel.: +8618831206858;
4
1789231720@qq.cm, Tel.: +8618730293191; 52625900191@qq.cm,
compound are more significant for the curative effect of Tel.: +8615930754411; 6532045956@qq.cm, Tel.: +8613315276505;
diabetes. Therefore, the experiment was conducted in 7
996989071@qq.cm, Tel.: +8613315276505

Pharmacodynamics Study on the Effect of Jerusalem artichoke Compound Granule Particles on type II diabetic mice
Zhang et al. 026

This experiment selected sealwort, Jerusalem artichoke, Determination of polysaccharides in Jerusalem


white mulberry root-bark, fenugreek, purslane, cinnamon artichokes
the six homology of medicine and food. They were used to
compose compound Chinese medicine, by drying, reflux By orthogonal results (Table 2), the influence degree of
extraction, enrichment of refined, spray drying, preparation each factor on the experiment is A>C>B. For A factor, K2 >
of particles. And the mouse model of type II diabetes was
established by intraperitoneal injection of streptozotocin K1 > K 3 , A2 is the optimal level. In the same respect, B1
after high-fat and high-sugar diets were administered to and C2 were the best. Therefore, the optimal protocol for
mice. (Lei Yang et al., 2014), to study the effect of Chinese the extraction of the Jerusalem artichoke composite
herbal medicines on reducing blood on type 2 diabetes (1000g) was A2B1C2. The best preparation process was
systematically. extracted twice, with each extraction time 90min, and the
water volume 10 times. The content of polysaccharide
MATERIALS AND METHODS could be obtained by using anthrone sulfuric acid method
(Xu BB et al., 2015). The polysaccharide content in the
Medicinal plant final preparation was 268.4mg•g-1.

The plants of sealwort, Jerusalem artichoke, white The preparation of the composite particles
mulberry root-bark, fenugreek, purslane, cinnamon was
derived from Guowei Zhang (Department of Chinese The purchased medicinal materials were cut and
Medicine of HeBei University). pulverized by pulverizer, according to the best scheme
mentioned above, the solution was concentrated into the
The optimization process of Jerusalem artichoke extract. 10g extract was used for the determination of
composite particles polysaccharide content, and the rest of the extract was
sprayed with SY-6000 small spray dryer to make the
On the basis of single factor experiment, we selected composition of traditional Chinese medicine (Pingping Wu
distilled water volume fraction, extraction time and et al., 2014).
extraction times to be the examined factors, with each
factor in three levels. According to the orthogonal Table of Experimental Animals
L9 (34), the polysaccharide yield of the composite particles
was determined, the factor level (Table 1), test arrangement Male SPF mice were purchased from the experimental
and result (Table 2). animal center of Hebei Medical University (Beijing, China).
Table 1: Factors and levels of L9 (34) orthogonal design All animals were maintained under standard environment
Level Factor conditions (23 ± 2°C, 55 ± 5% humidity and 12-h/12-h
Distillation Distillation Water light/dark cycle) (Leiria LO et al., 2011).
time/min time/times quantities/time
The establishment of animal models
(A) (B) (C)
1 60 1 10 The mice were fed adaptively for 3 days and then randomly
2 90 2 15 grouped by weight, and 9 of them were treated as a blank
3 120 3 20 control group for standard diet, while the remaining mice
fed high-fat diet. After 3 weeks, fasted but free access to
Table 2: Results of inulin content determination (mg/g) water for 12 hours, they were given intraperitoneal
Test Factor Inulin injection of 125 mg·kg-1 dose STZ (STZ soluble in 0. 1
Number A B C D Content mol · L-1 pH 4.2 citric acid/sodium citrate buffer, is active,
mg/g
ice bath), fed high-fat diet for 4 weeks, and then fasted but
1 1 1 1 1 240.2500
could drink water for 12 hours. A glucometer was used to
2 1 2 2 2 248.0950
3 1 3 3 3 255.8500
measure blood sugar, and mice with FBG reaching
4 2 1 2 3 268.4000 11.1mmol/L were regarded as successful models (Li JL et
5 2 2 3 1 252.6530 al., 2014, Leiria LO et al., 2011). 45 successful modeling
6 2 3 1 2 247.9320 mice were divided into five groups by average weight
7 3 1 3 2 235.0023 randomly: the model group, the positive control group, the
8 3 2 1 3 230.2780 low-dose group, the medium dose group and the high-
9 3 3 2 1 227.7803 dose group, with each group consisting of 9. The following
248.0650 247.8841 239.4867 day, the mice were given corresponding dose drugs, with
K1 each mouse given 2mL/100g corresponding drugs. The
256.3283 243.6753 248.0918 blank control group and the model group were given
K2
231.0202 243.6753 247.8351 distilled water, the positive control group for glyburide, and
K3 the drug concentrations in the high, middle and low dose
Rj 25.3081 4.2088 8.6051 groups were respectively 3000 mg/kg, 1500 mg/kg and

Pharmacodynamics Study on the Effect of Jerusalem artichoke Compound Granule Particles on type II diabetic mice
Int. J. Herbs, Spices Med. Plants 027

750 mg/kg. They were gavaged once a day for four weeks The situation of Ⅱ diabetes mice
excluding the mice died in the experiment (Lei Yang et al.,
2014). A total of 45 mice were successfully modeled. The weight
of the mice with the successful modeling were less than
Specimen collection those in the blank control group (Figure 1), and the food
intake was larger than that of the blank control group
After the last lavage administration, each group of mice (Figure 2). And after the treatment, the weight of the high
were fasted but could drink water for 12 hours. Blood was dose group, the medium dose group, the low dose group
extracted from the eyeball, and heparin was added and the positive group compared with before has
respectively. The centrifuge was 3000r·min-1 for 10 increased, its change was statistically significant (P < 0.05),
minutes (Holvoet, P et al., 1998, He HJ et al., 2012), and The food intake compared with their previous weight has
then plasma was extracted to determine absorbance at decreased, and its change was statistically significant (P <
620 nm and calculate SOD and MDA content. 0.05). The weight and food intake of the model group didn’t
change clearly (P > 0.05).
The blood glucose in mice
Effects of Jerusalem artichoke compound particles on
During the experiment, the fasting blood glucose was the fasting glucose (FBG) in diabetic mice
measured by a roche glucometer on the 1st, 10th, 20th,
and 30th days of fasting. Compared with the blank control group, the blood glucose
level of mice after successfully modeling was significantly
Statistical Analysis higher (P<0.05). Within 4 weeks after administration,
compared with the model group, the high, medium and low
The results of the experiment were expressed by x±s, and dose groups which were given the Jerusalem artichoke
a single factor variance analysis was performed by compound particles and the positive group which was
SPSS13.0 statistical software. A value of p<0.05 was given glyburide, of which blood sugar levels after 10, 20,
considered statistically significant. 30 days reduced gradually, has significant difference at 30
days (Table 3 and Figure 3).

RESULTS Effects of compound composition of Jerusalem


artisan compound on SOD and MDA in serum
Optimal process of Jerusalem artichoke compound
particles After administration, compared with the model group, the
levels of MDA in the positive group, the middle-dose group
The optimal experimental scheme was obtained from the and the low-dose group significantly decreased (P<0.05),
orthogonal experiment, which was extracted twice, 90 and the SOD level increased significantly (P<0.05). There
minutes each time, and the water amount was 10 times. was no significant difference in the high-dose group
The polysaccharide content in the final preparation was (P>0.05) (Figure 4 and 5).
268.4mg·g-1.

Figure 1: Effects on the weight(g) of mice after administration

Pharmacodynamics Study on the Effect of Jerusalem artichoke Compound Granule Particles on type II diabetic mice
Zhang et al. 028

Figure 2: Effect on food intake(g) of mice after administration

Figure 3: Effect on blood glucose(mmol/L) of mice after administration

Table 3: Effect on blood glucose(mmol/L) of mice after administration (x + s)

Pharmacodynamics Study on the Effect of Jerusalem artichoke Compound Granule Particles on type II diabetic mice
Int. J. Herbs, Spices Med. Plants 029

Figure 4: Effect on MDA content (nmol/ml) of mice after administration

Figure 5: Effect on SOD content (U/ml) after administration

DISCUSSION activity, increase the level of free radicals, and further


aggravate the patient’s sugar and lipid metabolism (Liu YL
In the experiment, streptozotocin is a free radical activator, et al., 2016). Under normal circumstances, the body's
which can selectively destroy islet cells and cause glucose production and elimination can maintain dynamic balance
metabolism disorder, so it can cause hyperglycemia and without causing damage to the body. In diabetes, the
diabetic symptom (KIHO T et al., 2002). In this experiment, oxidative stress induced by hyperglycemia increases, and
the mice models of type II diabetes were successfully the scavenging ability of the body decreases, resulting in
established by intraperitoneal injection of STZ in mice fed damage to the tissue cells. It has been reported that the
with high-fat and high-sugar diets.
MDA content of type Ⅱ diabetes population on the
Studies have shown that oxidative stress is closely related average is higher than that of the general population (Yin
to the course of diabetes (Young-Min Lee et al., 2009). SL et al., 2010. Du XX et al., 2013), SOD activity was
SOD and MDA are markers of oxidative stress (Fujita H et significantly lower than that in healthy people, so the
al., 2012.). On the one hand, diabetic hyperglycemia had peroxide stress significantly higher than that in healthy
antioxidants proteins in defense enzyme for scavenging of people. Oxidative stress can affect the body's antioxidant
bodily free radicals inactivated, reduced activity, and enzyme activity, and increase the level of free radicals,
eventually destroyed, the normal oxidation-oxidation further aggravating patient sugar and lipid metabolism
system balance, so the body enhanced oxidative stress (Shen BQ et al., 2014).
level, inhibiting energy metabolism and reducing
membrane island element synthesis and secretion. On the In this experiment, it was found that by lavage Jerusalem
other hand, oxidative stress signaling pathways activated artichoke compound combination, the SOD level in the
could decrease the peripheral tissue sensitivity to rancid high-dose, middle-dose and low-dose groups significantly
inolin and the membrane island effect to further strengthen increased, and the MDA level decreased significantly.
the resistance of membrane island element. Therefore, Especially the middle dose group is the most obvious, and
oxidative stress can affect the body's antioxidant enzyme it was similar to the positive group.

Pharmacodynamics Study on the Effect of Jerusalem artichoke Compound Granule Particles on type II diabetic mice
Zhang et al. 030

CONCLUSIONS metabolism in normal mouse liver. Planta Med. 112(6):


393-400.
The Jerusalem artichoke compound granule particles has Lei Yang, Yi Shu. (2014). The hypoglycemic effect of
retained the full and powerful hypoglycemic effect, which puerarin on diabetic mice induced by streptozotocin.
is strongly supported using in folk medicine and promoting Journal of Chinese hospital pharmacy. 16:1339.
the development of new therapeutics based on natural Leiria LO, Mónica FZ, Carvalho FD et al (2011). Functional,
products. morphological and molecular characterization of
bladder dysfunction in streptozotocin-induced diabetic
mice: evidence of a role for L-type voltage-operated
ACKNOWLEDGEMENTS Ca2+ channels. British journal of pharmacology.
163(6):1276-88.
This study was supported by the innovation and Li JL. (2014). Study on glucolipid metabolism and its
entrepreneurship project of Hebei University (grant mechanism in mice with insulin resistance model of
numbers: 2017156). The authors wish to thank Guowei type Ⅱ diabetes mellitus. Guangzhou university of
Zhang (M.D. and Ph.D., China) for his invaluable traditional Chinese medicine.
assistance. We gratefully acknowledge Xianmao Liang Liu LY. (2016). Effects of dioscorea dioscorea on serum
(senior experimental, Chinese medicine identification SOD and MDA in patients with type Ⅱ diabetes. Fujian
teaching and research section of Hebei University) for university of traditional Chinese medicine.
identifying sealwort, Jerusalem artichoke, white mulberry Pingping Wu, Qian Deng, Guangzhi Ma, et al. (2014).
root-bark, fenugreek, purslane, cinnamon as authentic Spray Drying of Rhodomyrtus tomentosa (Ait.) Hassk.
plants. And we also acknowledge the Pharmacodynamic Flavonoids Extract: Optimization and Physicochemical,
study of Jerusalem artichoke particles in type I and II Morphological, and Antioxidant Properties. Int J Food
diabetic rat models of Bo Zhao,which provided Research Sci.
experience to us. Shen BQ, Shen QS, Zhang QZ, et al. (2014). The
We had full access to all of the data in the study and takes relationship between oxidative stress and diabetic
responsibility for the integrity of the data and the accuracy vascular complications. Chinese diabetes magazine.
of the data analysis. 22(9):856-858.
Vandam RB, Willett WC, Rimm EB. (2002). Dietary fat and
meat intake inrelation to risk of typeⅡdiabetes in men
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Pharmacodynamics Study on the Effect of Jerusalem artichoke Compound Granule Particles on type II diabetic mice

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