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International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32
29 | P a g e
STUDY OF PATHOLOGICAL, EFFECTS OF
CRUDE EXTRACT OF PORTULACA OLERACEA
L. IN THE ALBINO MICE ORGANS
Khalil H. Aljeboori*, Omar H. Khalaf AL-Rubai* and Nahi, Y. Yassen**
*Dept. of pathology, College of Veterinary medicine,
University of Baghdad
**Iraqi center for cancer & Medical Genetics Research,
University of AL–Mustanseraia.
Abstract— This study was designed to evaluate the effect of
70% ethanolic crude extract of Portulaca oleracea L on mice
orgons . (In vivo),In vivo, the acute toxicity of 70 % ethanolic
extract of the plant on normal mice was studied. No toxic effect
was noted on normal mice even at 9500 mg /kg B.W S/C
injection.Histopathological changes due to ethanolic extract of
the plant in healthy mice were summarized in hyperplasia of
white pulp with amyloid deposition, proliferation of
megakaryocytes and mononuclear cell infiltration in the liver and
kidney parenchyma. There were no significant lesions detected in
the brain, heart and ovary in all treated groups.
Key Words— Portulaca oleracea (purslane), effect in mice
orgins
I. INTRODUCTION
A. Chemical compounds of Portulaca oleracea
Purslane appears to be the only higher plant reported to
contain the beneficial omega-3 fatty acids (O3FAs) -
eicosapentaenoic acid (EPA) and docosahexaenoic acid
(DHA). Purslane also contains carbohydrates, lipids,
glycosides, alkaloids, sterols, triterpenes, and flavonoids (1).
Phenolic constituents of the plant include scopoletin,
bergapten, isopimpinellin, lonchocarpic acid, robustin,
genistein, and others (2). Purslane is a rich source of vitamins
A, B, C, and E (3). Purslane is high in carotenoid content,
including beta-carotene (4), (5).
Purslane contains large amount of norepinephrine
(noradrenalin), dopa, dopamine, citric acid,waxes, tannic acid,
alkaloid, flavinoid, coumarone, saponines, cardiac glycoside,
amino acid, anthraquin, oxilic acid (6, 7) determined levels of
endogenous antioxidants (alpha-tocopherol, ascorbic acid,
beta-carotene and glutathione) in plant leaves. In addition, it
was (8) showed that portulaca oleracea have antioxidant and
free radical scavenging activities.
Portulaca oleracea L. (PO) It is an edible plant and is
usually cut into small pieces and eaten with salt (9). In the
United Arab Emirates and Oman, a cultivated variety of PO is
used as a vegetable (10). Portulaca oleracea L, has many
folkloric uses, it is used in the Arabian Peninsula as antiseptic,
anti-scorbutic, antispasmodic (10). In China, it is used as an
anti-bacterial and anti-viral agent and for the treatment of viral
hepatitis and in diabetes management (11). Portulaca oleracea
L showed a tumoricidal activity against KATO III (human
gastric carcinoma cell (line) and COLO 320 HSR cells (human
colon adenoma cell line) in vivo and in vitro (12, 13) Purslane
acts as analgesic, antiarthritic, antiartheriosclerotic and
anticancer (breast, colon, forestomach, liver, skin) activities.
(14) Mentioned that Polysaccharide from Portulaca oleracea L.
has immune effects on mice with tumor S180.
This study was designed to asses the pathological effect of
portulaca oleracea crude extract in albino mice organs.
II. MATERIALS AND METHODS
A. Experimental animals for LD50
Nineteen adult Swiss albino balb/C mice (range of body
weight=25-30g) were used to determine the subcutaneous
median lethal dose (LD50) of ethanolic extract of Portulaca
oleracea .
B. Determination of LD50
Graduated doses of Portulaca oleracea ethanolic extract
were dissolved in 10 ml distill water and administered S/C as
0.1 ml for each 10 gm of animal body weight. The range was
of S/C single doses used in the determination of LD50 of
extract was (5000- 9500) mg /kg B.W. Mortality was recorded
after 24 hrs and LD50 was calculated according to up and
down method described by (15) by employing the following:
LD50 =X f +KD Where: Xf is the last dose administered. K is
the tabular value, and D is the interval between doses.
C. Animals treated with ethanolic extract of Portulaca
oleracea
By returning to results of LD50, and values reported in
some references (12), the doses were adjusted in this study
(200 mg/ kg B .W. after S/C injection daily for 30 days.
International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32
30 | P a g e
D. The effect of ethanolic extract on healthy mice
Ten healthy female adult mice were used at 8-10 wks of
age and 25-30 gm B.W. for examining hisopathological
changes after treatment with ethanolic extract of P.O. These
animals were divided into 2 groups, each group had 5 animals
and as follows:
1. Five adult female albino mice were injected S/C daily
with 200 mg/g B.W. of ethanolic extract of P.O for 30
days.
2. Five adult female albino mice were injected S/C daily
with D. Was control group for 30 days.
E. Histopathology study
At the end of the experiment, the animals were sacrificed
and postmortem was done for all animals. The macroscopic
appearances were recorded to detect any abnormal gross
changes in internal organs. Specimens were taken from all
internal organs; the tissues were kept in 10% formaldehyde
immediately after removal. After 48 hours of the fixation, the
processing was routinely done with a set of increasing alcohol
concentrations, tissue section were embedded in paraffin
blocks, and sectioned by microtome at 5µm for all tissues. All
tissues were stained with hematoxylin and eosin stain and the
histopathological changes were observed under light
microscope (16).
III. RESULTS AND DISCUSSION
A. Median lethal Dose (LD 50)
Acute toxicity test of portulaca oleracea extract showed no
toxic symptoms on the animals when extracted by 70 %
ethanolic solution .Different doses ranging from (5000 to
9500) mg/kg B.W injected subcutaneously caused no deaths in
experimental mice. Portulaca oleracea was considered safe
even at high dosage (17).
B. Spleen of healthy mice treated with P.O only
Organ of this group showed extensive hyperplasia of white
pulp in the periarterial sheath (T-cell region), extensive
hyperplasia of remainder region of white pulp (B-cell region)
and amyloid deposition surround the follicles and proliferation
of megakaryocytes (Figure: 1-2;)
Figure 1: Histological section in spleen of healthy female
mice received 200mg/kg B.W S/C of P.O only for 30 days,
showing extensive hyperplasia in white pulp in the
periarterial sheath region (T-cell region) and extensive
hyperplasia of remainder region of white pulp (B-cell
region)and proliferation of megakaryocytes (100XH&E).
Figure 2: Histological section in spleen of healthy female
mice received 200 mg/kg. B.W S/C of P.O only, showing
hyperplasia in white pulp and amyloid deposition inclosed
the white pulp (200XH&E).
C. Liver of normal mice received ethanolic extract of P.O only
Liver of this group showing aggregation of mononuclear
cells to forming early pericentilobular granuloma, also
hydropic degeneration seen in hepatocytes (Figure: 3-4).
Figure 3: Histological section in liver of healthy female
mice received 200mg/k. B.W S/C of P.O only for 30 days
showing mononuclear cell aggregation to forming early
granuloma (200XH&E).
International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32
31 | P a g e
Figure 4: Histological section in liver of healthy female
mice received 200mg/k. B.W S/C of P.O only, at high
magnification of Figure 3 of early granuloma (400XH&E)
D. Kidney of normal mice received ethanolic extract of P.O
only
Kidneys in this group showing sever perivascular
infiltration of mononuclear cells (lymphocyte and macrophage)
in kidney paranchamia also hydropic degeneration of renal
tubules (Fig. 5).
Figure (5): Histological section in kidney of healthy female
mice received 200 mg/kg. B.W S/C of P.O only for 30 days,
Showing sever perivascular infiltration of mononuclear
cells (lymphocyte and macrophage) in kidney
paranchyamia (200XH&E).
Healthy mice treated with P.O only, showed hyperplasia of
white pulp and aggregation of mononuclear cell in liver
parenchyma and hydropic degeneration of hepatocytes and
sever perivascular infiltration of mononuclear cells
(lymphocyte and macrophage) in kidney paranchamia and
hydropic degeneration of renal tubules.
The 2nd lymphoid organs comprise the spleen, lymph
nodes and (Vinuesa and Cook. 2007). Liver had been
considered the largest reservoirs of CD+ 4 memory T cells in
mice after the effectors phase of an immune reaction (18, 19).
Portulaca oleracea have active compound like antioxidant,
flavonoid, catechine and alkaloids which may act as immune
stimulant and increased splenocyte proliferation (20, 21)
showed that spleen follicular hyperplasia due to catechines of
Camellia sinensis plant extract.
There was deposition of amyloid in spleen in the health
mice treated with P.O only and. Deposition of amyloid fibril
protein (Amyloid light chain) type is a (22), a ssociated with
some form of monoclonal B-cell proliferation nd proliferation
of megakaryocytes in their spleen as a result of response to
multiple cytokines (23), which secreting immune mediators to
enhance immune response.
Healthy mice treated with P.O that received 200 mg/kg.
B.W S/C of P.O only for 30 days, showed high mononuclear
cell infiltration between renal tubule as a result of high immune
complex compared with healthy mice treated only with distill
water that have no significant lesion detected. Also the role of
purslane extract components give toxic effect on epithelia such
as hepatocytes, renal epith. And cause cloudy swelling and
hydropic degeneration in addition the role of pursline extract
components like antioxidant, flavonoid, catechine and alkaloids
have immunological effect on ymphoid tissue couse spleen
hyperplasia and infiltration of mononuclear cells
(Lymphocytes and macrophages) in the liver and kidney (22).
REFERENCES
[1] Sayed, H. et al (1985). Pharmacognostical study of Portulaca
oleracea L. growing in Egypt. Part Ι: Botanical study of the
stems, leaves, and investigation of the lipid content. Bull Pharm
Sci.; 8:41-60.
[2] Awad N (1994) .Lipid content and antimicrobial activity of
phenolic constituents of cultivated Portulaca oleracea L. Bull
Fac Pharm. (32):137-142.
[3] Chevallier, A. (1996).The Encyclopedia of Medicinal Plants.
New York, NY: DK Publishing, 253.
[4] Guil-Guerrero J, et al., (1999). Lipids classes, fatty acids, and
carotenes of the leaves of six edible wild plants. Z Lebensm
Unters Forsch A.; 209:313-316.
[5] Liu, L. et al (2000). Fatty acids and β-carotene in Australian
purslane (Portulaca oleracea) varieties. J Chromatogr. 893:207-
213.
[6] Wattenberg, L. W. (1993). Inhibition of carcinogenesis by non-
nutrient constituents of the diet. In: Food and cancer prevention-
-chemical and biological aspects, edited by Waldron, K. W.,
Johnson, I. T., and Fenwick, G. R., The Royal Society of
Chemistry, Cambridge, U. K., pp. 12-23.
[7] Simopoulos A.P et al., (1992). Common Purslane: A source of
omega-3 fatty acids and antioxidants. J. Am. Col. Nutr. 11:374-
382
[8] Hutadilok- Towatana,N.; Chaiyamutti, P.; Mahabusarakam, W
.and Rukachaisirikul, V.(2006). Antioxidative and Free Radical
Scavenging Activities of Some Plants Used in Thai Folk
Medicine ,international Jour of pharmacognacy ,vol 44,Numb 3,
pp221- 228 ( 8 ) .
[9] Ghazanfar, S.A. (1994). Handbook of Arabian Medicinal
Plants.CRC Press, Boca Raton, FL, .p.176.
[10] Chan, K.;Islam, M.W.; Kamil, M.;Radhakrishnan, R.; Zakaria,
M.N.; Habibullah, M.and Attas, A. (2000). The analgesic and
anti-inflammatory effects of Portulaca oleracea L. subsp. Sativa
(Haw.) Celak. J Ethnopharmacol; 73:445-451.
International Journal of Technical Research and Applications e-ISSN: 2320-8163,
www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32
32 | P a g e
[11] Hu, LF. Xu, XY.;Wang, BQ.(2003).Research and utilization
situation of Portulaca Oleracea L in China. Prac J MED
&Pharm; 20:315-316
[12] Yoon, J.; Ham, S. S. and Jun H, S, (1999). Portulaca oleracea
and tumor cell growth. U S patent, patent Number 5.869.060.
[13] Esiyok, D.; Ötles, S.and Akcicek E, (2004). Herbs as a Food
Source in Turkey. Asian Pacific J Cancer Prev, 5, 334-339.
[14] Xiao-bo, W.; Dian-wu, L.; Li-qin, W.; Ben-hua, W.; Xiao-ru, L.
and Li-qin, X. (2005). Immune Effects of Polysaccharide from
Portulaca oleracea on Mice with Tumor S180, www. Ilibe.com
[15] Dixon, W.J. (1980): Efficient analysis of experimental
observations. Ann. Res. Pharmacol. Toxicol. 20: 441-462.
[16] Luna, L.G. (1968). Manual of Histological Staining Methods of
the Armed Forces Institute of Pathology. (3rd ed.).McGraw –
Hill Book Company. New York.
[17] Reid, D (1986): Chinese Herbal Medicine. Boston, MA:
Shambhala Publications, Inc., 56.
[18] Hamann, D.; Baars, P.A.; Rep, M.H.; Hooibrink, B.; Kerkhof-
Garde, S.R.,and Klein, M.R. (1997). Phenotypic and functional
separation of memory and effector human CD8+ T cells. J Exp
Med 186, 1407–1418.
[19] Singh, N.; Singh, S.P. and Nath, R. (1986). Prevention of
Urethan induced lung adenomas by Withania sonmifera (L),
Dunal in albino mice. Ind. J. Crude drug Res., 24:90 – 100.
[20] Kamath, A.B.;Wang,L and Das,H.(2003). Antigens in tea –
beverage prime human V gamma 2delta zt cells in vitro and
invivo for memory and nonmemory antibacterial cytokine
responses. Proc. Natl. Acad. Sci. (USA), 100:6009 – 6014.
[21] Umran, M, A. (2008). Influence of Polyphenols Extracts of
Green Tea Camellia sinensis on The Normal and Cancer Cells
Lines in Vivo and In Vitro. College of Science, Baghdad
University. Iraq.
[22] Kumar, V.; Abbas, A.K.; Cotran, R.S.and Robbins, S.L. (2007).
Robbins Basic Pathology (8thed).Saunders, Pennsylvania,
U.S.A. Pp: 165-210.
[23] Metcalf, D.; Mifsud, S. and Di Rago, L. (2002). Stem cell factor
can stimulate theformation of eosinophils by two types of
murine eosinophil progenitor cells.Stem Cells 20, 460–469.

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STUDY OF PATHOLOGICAL, EFFECTS OF CRUDE EXTRACT OF PORTULACA OLERACEA L. IN THE ALBINO MICE ORGANS

  • 1. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32 29 | P a g e STUDY OF PATHOLOGICAL, EFFECTS OF CRUDE EXTRACT OF PORTULACA OLERACEA L. IN THE ALBINO MICE ORGANS Khalil H. Aljeboori*, Omar H. Khalaf AL-Rubai* and Nahi, Y. Yassen** *Dept. of pathology, College of Veterinary medicine, University of Baghdad **Iraqi center for cancer & Medical Genetics Research, University of AL–Mustanseraia. Abstract— This study was designed to evaluate the effect of 70% ethanolic crude extract of Portulaca oleracea L on mice orgons . (In vivo),In vivo, the acute toxicity of 70 % ethanolic extract of the plant on normal mice was studied. No toxic effect was noted on normal mice even at 9500 mg /kg B.W S/C injection.Histopathological changes due to ethanolic extract of the plant in healthy mice were summarized in hyperplasia of white pulp with amyloid deposition, proliferation of megakaryocytes and mononuclear cell infiltration in the liver and kidney parenchyma. There were no significant lesions detected in the brain, heart and ovary in all treated groups. Key Words— Portulaca oleracea (purslane), effect in mice orgins I. INTRODUCTION A. Chemical compounds of Portulaca oleracea Purslane appears to be the only higher plant reported to contain the beneficial omega-3 fatty acids (O3FAs) - eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). Purslane also contains carbohydrates, lipids, glycosides, alkaloids, sterols, triterpenes, and flavonoids (1). Phenolic constituents of the plant include scopoletin, bergapten, isopimpinellin, lonchocarpic acid, robustin, genistein, and others (2). Purslane is a rich source of vitamins A, B, C, and E (3). Purslane is high in carotenoid content, including beta-carotene (4), (5). Purslane contains large amount of norepinephrine (noradrenalin), dopa, dopamine, citric acid,waxes, tannic acid, alkaloid, flavinoid, coumarone, saponines, cardiac glycoside, amino acid, anthraquin, oxilic acid (6, 7) determined levels of endogenous antioxidants (alpha-tocopherol, ascorbic acid, beta-carotene and glutathione) in plant leaves. In addition, it was (8) showed that portulaca oleracea have antioxidant and free radical scavenging activities. Portulaca oleracea L. (PO) It is an edible plant and is usually cut into small pieces and eaten with salt (9). In the United Arab Emirates and Oman, a cultivated variety of PO is used as a vegetable (10). Portulaca oleracea L, has many folkloric uses, it is used in the Arabian Peninsula as antiseptic, anti-scorbutic, antispasmodic (10). In China, it is used as an anti-bacterial and anti-viral agent and for the treatment of viral hepatitis and in diabetes management (11). Portulaca oleracea L showed a tumoricidal activity against KATO III (human gastric carcinoma cell (line) and COLO 320 HSR cells (human colon adenoma cell line) in vivo and in vitro (12, 13) Purslane acts as analgesic, antiarthritic, antiartheriosclerotic and anticancer (breast, colon, forestomach, liver, skin) activities. (14) Mentioned that Polysaccharide from Portulaca oleracea L. has immune effects on mice with tumor S180. This study was designed to asses the pathological effect of portulaca oleracea crude extract in albino mice organs. II. MATERIALS AND METHODS A. Experimental animals for LD50 Nineteen adult Swiss albino balb/C mice (range of body weight=25-30g) were used to determine the subcutaneous median lethal dose (LD50) of ethanolic extract of Portulaca oleracea . B. Determination of LD50 Graduated doses of Portulaca oleracea ethanolic extract were dissolved in 10 ml distill water and administered S/C as 0.1 ml for each 10 gm of animal body weight. The range was of S/C single doses used in the determination of LD50 of extract was (5000- 9500) mg /kg B.W. Mortality was recorded after 24 hrs and LD50 was calculated according to up and down method described by (15) by employing the following: LD50 =X f +KD Where: Xf is the last dose administered. K is the tabular value, and D is the interval between doses. C. Animals treated with ethanolic extract of Portulaca oleracea By returning to results of LD50, and values reported in some references (12), the doses were adjusted in this study (200 mg/ kg B .W. after S/C injection daily for 30 days.
  • 2. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32 30 | P a g e D. The effect of ethanolic extract on healthy mice Ten healthy female adult mice were used at 8-10 wks of age and 25-30 gm B.W. for examining hisopathological changes after treatment with ethanolic extract of P.O. These animals were divided into 2 groups, each group had 5 animals and as follows: 1. Five adult female albino mice were injected S/C daily with 200 mg/g B.W. of ethanolic extract of P.O for 30 days. 2. Five adult female albino mice were injected S/C daily with D. Was control group for 30 days. E. Histopathology study At the end of the experiment, the animals were sacrificed and postmortem was done for all animals. The macroscopic appearances were recorded to detect any abnormal gross changes in internal organs. Specimens were taken from all internal organs; the tissues were kept in 10% formaldehyde immediately after removal. After 48 hours of the fixation, the processing was routinely done with a set of increasing alcohol concentrations, tissue section were embedded in paraffin blocks, and sectioned by microtome at 5µm for all tissues. All tissues were stained with hematoxylin and eosin stain and the histopathological changes were observed under light microscope (16). III. RESULTS AND DISCUSSION A. Median lethal Dose (LD 50) Acute toxicity test of portulaca oleracea extract showed no toxic symptoms on the animals when extracted by 70 % ethanolic solution .Different doses ranging from (5000 to 9500) mg/kg B.W injected subcutaneously caused no deaths in experimental mice. Portulaca oleracea was considered safe even at high dosage (17). B. Spleen of healthy mice treated with P.O only Organ of this group showed extensive hyperplasia of white pulp in the periarterial sheath (T-cell region), extensive hyperplasia of remainder region of white pulp (B-cell region) and amyloid deposition surround the follicles and proliferation of megakaryocytes (Figure: 1-2;) Figure 1: Histological section in spleen of healthy female mice received 200mg/kg B.W S/C of P.O only for 30 days, showing extensive hyperplasia in white pulp in the periarterial sheath region (T-cell region) and extensive hyperplasia of remainder region of white pulp (B-cell region)and proliferation of megakaryocytes (100XH&E). Figure 2: Histological section in spleen of healthy female mice received 200 mg/kg. B.W S/C of P.O only, showing hyperplasia in white pulp and amyloid deposition inclosed the white pulp (200XH&E). C. Liver of normal mice received ethanolic extract of P.O only Liver of this group showing aggregation of mononuclear cells to forming early pericentilobular granuloma, also hydropic degeneration seen in hepatocytes (Figure: 3-4). Figure 3: Histological section in liver of healthy female mice received 200mg/k. B.W S/C of P.O only for 30 days showing mononuclear cell aggregation to forming early granuloma (200XH&E).
  • 3. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32 31 | P a g e Figure 4: Histological section in liver of healthy female mice received 200mg/k. B.W S/C of P.O only, at high magnification of Figure 3 of early granuloma (400XH&E) D. Kidney of normal mice received ethanolic extract of P.O only Kidneys in this group showing sever perivascular infiltration of mononuclear cells (lymphocyte and macrophage) in kidney paranchamia also hydropic degeneration of renal tubules (Fig. 5). Figure (5): Histological section in kidney of healthy female mice received 200 mg/kg. B.W S/C of P.O only for 30 days, Showing sever perivascular infiltration of mononuclear cells (lymphocyte and macrophage) in kidney paranchyamia (200XH&E). Healthy mice treated with P.O only, showed hyperplasia of white pulp and aggregation of mononuclear cell in liver parenchyma and hydropic degeneration of hepatocytes and sever perivascular infiltration of mononuclear cells (lymphocyte and macrophage) in kidney paranchamia and hydropic degeneration of renal tubules. The 2nd lymphoid organs comprise the spleen, lymph nodes and (Vinuesa and Cook. 2007). Liver had been considered the largest reservoirs of CD+ 4 memory T cells in mice after the effectors phase of an immune reaction (18, 19). Portulaca oleracea have active compound like antioxidant, flavonoid, catechine and alkaloids which may act as immune stimulant and increased splenocyte proliferation (20, 21) showed that spleen follicular hyperplasia due to catechines of Camellia sinensis plant extract. There was deposition of amyloid in spleen in the health mice treated with P.O only and. Deposition of amyloid fibril protein (Amyloid light chain) type is a (22), a ssociated with some form of monoclonal B-cell proliferation nd proliferation of megakaryocytes in their spleen as a result of response to multiple cytokines (23), which secreting immune mediators to enhance immune response. Healthy mice treated with P.O that received 200 mg/kg. B.W S/C of P.O only for 30 days, showed high mononuclear cell infiltration between renal tubule as a result of high immune complex compared with healthy mice treated only with distill water that have no significant lesion detected. Also the role of purslane extract components give toxic effect on epithelia such as hepatocytes, renal epith. And cause cloudy swelling and hydropic degeneration in addition the role of pursline extract components like antioxidant, flavonoid, catechine and alkaloids have immunological effect on ymphoid tissue couse spleen hyperplasia and infiltration of mononuclear cells (Lymphocytes and macrophages) in the liver and kidney (22). REFERENCES [1] Sayed, H. et al (1985). Pharmacognostical study of Portulaca oleracea L. growing in Egypt. Part Ι: Botanical study of the stems, leaves, and investigation of the lipid content. Bull Pharm Sci.; 8:41-60. [2] Awad N (1994) .Lipid content and antimicrobial activity of phenolic constituents of cultivated Portulaca oleracea L. Bull Fac Pharm. (32):137-142. [3] Chevallier, A. (1996).The Encyclopedia of Medicinal Plants. New York, NY: DK Publishing, 253. [4] Guil-Guerrero J, et al., (1999). Lipids classes, fatty acids, and carotenes of the leaves of six edible wild plants. Z Lebensm Unters Forsch A.; 209:313-316. [5] Liu, L. et al (2000). Fatty acids and β-carotene in Australian purslane (Portulaca oleracea) varieties. J Chromatogr. 893:207- 213. [6] Wattenberg, L. W. (1993). Inhibition of carcinogenesis by non- nutrient constituents of the diet. In: Food and cancer prevention- -chemical and biological aspects, edited by Waldron, K. W., Johnson, I. T., and Fenwick, G. R., The Royal Society of Chemistry, Cambridge, U. K., pp. 12-23. [7] Simopoulos A.P et al., (1992). Common Purslane: A source of omega-3 fatty acids and antioxidants. J. Am. Col. Nutr. 11:374- 382 [8] Hutadilok- Towatana,N.; Chaiyamutti, P.; Mahabusarakam, W .and Rukachaisirikul, V.(2006). Antioxidative and Free Radical Scavenging Activities of Some Plants Used in Thai Folk Medicine ,international Jour of pharmacognacy ,vol 44,Numb 3, pp221- 228 ( 8 ) . [9] Ghazanfar, S.A. (1994). Handbook of Arabian Medicinal Plants.CRC Press, Boca Raton, FL, .p.176. [10] Chan, K.;Islam, M.W.; Kamil, M.;Radhakrishnan, R.; Zakaria, M.N.; Habibullah, M.and Attas, A. (2000). The analgesic and anti-inflammatory effects of Portulaca oleracea L. subsp. Sativa (Haw.) Celak. J Ethnopharmacol; 73:445-451.
  • 4. International Journal of Technical Research and Applications e-ISSN: 2320-8163, www.ijtra.com Volume 2, Issue 1 (jan-feb 2014), PP. 29-32 32 | P a g e [11] Hu, LF. Xu, XY.;Wang, BQ.(2003).Research and utilization situation of Portulaca Oleracea L in China. Prac J MED &Pharm; 20:315-316 [12] Yoon, J.; Ham, S. S. and Jun H, S, (1999). Portulaca oleracea and tumor cell growth. U S patent, patent Number 5.869.060. [13] Esiyok, D.; Ötles, S.and Akcicek E, (2004). Herbs as a Food Source in Turkey. Asian Pacific J Cancer Prev, 5, 334-339. [14] Xiao-bo, W.; Dian-wu, L.; Li-qin, W.; Ben-hua, W.; Xiao-ru, L. and Li-qin, X. (2005). Immune Effects of Polysaccharide from Portulaca oleracea on Mice with Tumor S180, www. Ilibe.com [15] Dixon, W.J. (1980): Efficient analysis of experimental observations. Ann. Res. Pharmacol. Toxicol. 20: 441-462. [16] Luna, L.G. (1968). Manual of Histological Staining Methods of the Armed Forces Institute of Pathology. (3rd ed.).McGraw – Hill Book Company. New York. [17] Reid, D (1986): Chinese Herbal Medicine. Boston, MA: Shambhala Publications, Inc., 56. [18] Hamann, D.; Baars, P.A.; Rep, M.H.; Hooibrink, B.; Kerkhof- Garde, S.R.,and Klein, M.R. (1997). Phenotypic and functional separation of memory and effector human CD8+ T cells. J Exp Med 186, 1407–1418. [19] Singh, N.; Singh, S.P. and Nath, R. (1986). Prevention of Urethan induced lung adenomas by Withania sonmifera (L), Dunal in albino mice. Ind. J. Crude drug Res., 24:90 – 100. [20] Kamath, A.B.;Wang,L and Das,H.(2003). Antigens in tea – beverage prime human V gamma 2delta zt cells in vitro and invivo for memory and nonmemory antibacterial cytokine responses. Proc. Natl. Acad. Sci. (USA), 100:6009 – 6014. [21] Umran, M, A. (2008). Influence of Polyphenols Extracts of Green Tea Camellia sinensis on The Normal and Cancer Cells Lines in Vivo and In Vitro. College of Science, Baghdad University. Iraq. [22] Kumar, V.; Abbas, A.K.; Cotran, R.S.and Robbins, S.L. (2007). Robbins Basic Pathology (8thed).Saunders, Pennsylvania, U.S.A. Pp: 165-210. [23] Metcalf, D.; Mifsud, S. and Di Rago, L. (2002). Stem cell factor can stimulate theformation of eosinophils by two types of murine eosinophil progenitor cells.Stem Cells 20, 460–469.