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Evidence-Based Complementary and Alternative Medicine
Volume 2014 (2014), Article ID 326107, 11 pages
Review Article

A Review of Botanical Characteristics, Traditional Usage, Chemical Components, Pharmacological Activities, and Safety of Pereskia bleo (Kunth) DC

1Department of Pharmacy, Faculty of Science, National University of Singapore, 18 Science Drive 4, Singapore 117543
2Department of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597

Received 19 February 2014; Accepted 2 May 2014; Published 3 June 2014

Academic Editor: Wei Jia

Copyright © 2014 Sogand Zareisedehizadeh et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Pereskia bleo, a leafy cactus, is a medicinal plant native to West and South America and distributed in tropical and subtropical areas. It is traditionally used as a dietary vegetable, barrier hedge, water purifier, and insect repellant and for maintaining health, detoxification, prevention of cancer, and/or treatment of cancer, hypertension, diabetes, stomach ache, muscle pain, and inflammatory diseases such as dermatitis and rheumatism. The aim of this paper was to provide an up-to-date and comprehensive review of the botanical characteristics, traditional usage, phytochemistry, pharmacological activities, and safety of P. bleo. A literature search using MEDLINE (via PubMed), Science direct, Scopus and Google scholar and China Academic Journals Full-Text Database (CNKI) and available eBooks and books in the National University of Singapore libraries in English and Chinese was conducted. The following keywords were used: Pereskia bleo, Pereskia panamensis, Pereskia corrugata, Rhodocacus corrugatus, Rhodocacus bleo, Cactus panamensis, Cactus bleo, Spinach cactus, wax rose, Perescia, and Chinese rose. This review revealed the association between the traditional usage of P. bleo and reported pharmacological properties in the literature. Further investigation on the pharmacological properties and phytoconstituents of P. bleo is warranted to further exploit its potentials as a source of novel therapeutic agents or lead compounds.

1. Introduction

Pereskia bleo is a medicinal plant of the family Cactaceae. Cacti are well-known desert plants and widely recognized by their specialized growth form of the stems and leaves. This family consists of 100 genera and about 2000 species [1, 2]. The genus Pereskia consists of 17 species with regular leaf development and function. They are generally representative of the “ancestral cactus.” This genus does not look much like other types of cacti because of having substantial leaves and thin stems [35]. The plants in the genus Pereskia originate from the region between Brazil and Mexico and South America and Central America [68] and are cultivated in many tropical and subtropical countries including India, Malaysia, Singapore, and Indonesia [1]. They also generally resemble other types of plants such as roses [3, 8]. Pereskia species are divided into Clades A and B [9] (Table 1). The two clades of Pereskia differ in their geographical distribution. Clade A is found around the Gulf of Mexico and the Caribbean Sea whereas Clade B is found in the south of the Amazon Basin. The stems of the species of Pereskia within Clade A begin to form bark early in the life of the plant like most non-cacti. In contrast, Pereskia species within Clade B typically delay forming bark, thus giving the stem the potential to become a major organ for photosynthesis [4].

Table 1: Clades of the genus Pereskia [9].

Among them, Pereskia aculeata Mill (P. aculeate), Pereskia grandifolia Haw (P. grandifolia), and Pereskia bleo (Kunth) DC. (P. bleo) are listed to be found in Singapore and Malaysia [7, 10, 11]. P. bleo and P. grandifolia are used for medicinal purposes in these areas [1, 11]. Hence, more information on these three species is presented below.

1.1. Pereskia aculeata Mill

Its common names are Barbados gooseberry or lemon vine [12, 13] and it is native to tropical America [14]. This plant is a scrambling vine growing to the height of 10 m to a tree. The stems reach 2-3 cm in diameter. Younger stems have hooked thorns and older stems have clusters of woody spines. The leaves are 4–11 cm long and 1.5–4 cm wide, simple, and deciduous in the dry season. The flowers are white, cream, or pinkish with 2.5–5 cm diameter and strongly scented. This plant has translucent rounded white to pink berries which turn to yellow or orange with the diameter of 2 cm upon ripening. The fruits are edible and containing numerous small seeds. They somewhat resemble the gooseberry in appearance and are of excellent flavor [15, 16]. The leaves are also edible and are a popular vegetable in parts of the Brazilian state of Minas Gerais under the name of ora-pro-nóbis [14].

1.2. Pereskia grandifolia Haw

It is also known as rose cactus or Rhodocactus grandifolia. This plant is native to the Northeastern Brazil restingas and is cultivated in tropical and subtropical areas [7]. It is a shrub or small tree, 2–5 m high, with a grayish-brown trunk up to 20 cm in diameter. The spines range from black to brown and their number at each areole gradually increases with age. The new twigs may be spineless while the trunk may have up to 90 spines in areoles, each 2–6.5 cm long. The leaves vary in size from 9 to 23 cm long and the shapes range from elliptic to ovate and obovate-lanceolate. Usually 10–15 flowers of dense inflorescence develop at the ends of stems, but sometimes there are 30 or more. The flowers are pink-purple and look like rose with 3–5 cm diameter [12]. The leaves of P. grandifolia are edible [11].

1.3. Pereskia bleo (Kunth) DC

P. bleo is also known as Cactus bleo and has been commonly used for a variety of medicinal and non-medicinal purposes in different countries [1, 2]. However, to the best of our knowledge, a comprehensive review of P. bleo is not available. The objective of this paper is to provide a comprehensive review of the botanical characteristics, traditional usage, phytoconstituents, pharmacological activities, and safety of P. bleo. Such information will serve as a useful resource for the proper usage of this plant and for future research.

2. Method

Internet sources including MEDLINE (via Pubmed), Science direct, Scopus and Google scholar, and China Journals Full-Text Database (via CNKI) were searched for publications on this plant. The following keywords were used: Pereskia bleo, Pereskia panamensis, Pereskia corrugata, Rhodocactus corrugatus, Rhodocactus bleo, Cactus panamensis, Cactus bleo, Spinach cactus, wax rose, Perescia, and Chinese rose. No restriction on the language and date of publication was implemented. In addition, available books and eBooks in the National University of Singapore (NUS) libraries were manually searched for the relevant information.

3. Results and Discussion

3.1. Botanical Characteristics

P. bleo belongs to the order of Caryophyllales Juss. ex Bercht. & J. Presl, superorder of Caryophyllanae Takht and subclass of Magnoliidae Novák ex Takht. It is in the Cactaceae family, Peresioideae subfamily, and Pereskia Mill genus [44, 45]. In the International Plant Nomenclature Index (IPNI) [46], its ID code is 273592-2 and its basionym is Cactus bleo (Kunth). Basionym name is defined as “previously published legitimate name-bringing or epithet-bringing synonym from which a new name is formed for a taxon of different rank or position taxon of different rank or position” [17]. The scientific and common names of P. bleo are listed in Table 2. This plant is also known as “Pokok Jarum Tujuh Bilah” in Malay and “Cak Sing Cam” or “Qi Xing Zhen ()” in Chinese [8, 40]. Its Chinese name literally means “seven stars needle” [7].

Table 2: Scientific and common names of P. bleo.

P. bleo originates from Mesoamerica (Panama), Western South America (Columbia) [1, 2, 6, 12] and is distributed in tropical and subtropical regions [1, 2]. It is a deciduous, shrubby, tree-like plant with a height of 0.6–8 m. The trunk reaches 10 cm in diameter and bears very large fascicle of spines when it is young. However, the trunk becomes naked when turning old. Young branches are red and leafy and often bear 5–7 black spines up to 1 cm in length. The spines reach 2 cm on the older stems. The leaves are thin, oblong to oblanceolate, glossy, and succulent, 6–21 cm long, and 2–7 cm wide [2]. The flowers are orange-red and grouped in 2–4 terminally and laterally. The fruits are yellow, thick walled, fleshy, and glossy and look like conical berries at maturity, up to 5 × 5 cm in size, turbinate, and containing 6–8 mm in diameter dark brown or black color seeds [1, 19, 31]. It can be propagated by stem cutting or seeds [12].

This species was collected by Bonpland during Humboldt’s trip through the new world and was described and published by Kunth in 1823 [2]. In some older books and herbaria, it was confused with Pereskia grandifolia (P. grandifolia) [20] because both plants are vegetatively similar [31]. In addition, P. bleo and P. grandifolia are the only exceptions of Pereskia which grow in areas receiving considerably high annual rainfall more than 187 mm per wet month. Other Pereskia species grow in dry areas [3]. The two species can be distinguished by the leaves, flowers, and spines. P. bleo has thinner, corrugated leaves and orange-red flowers, with shorter spines compared to P. grandifolia. In contrast, P. grandifolia has thicker, uncorrugated leaves, pink to purplish-pink flowers and longer but fewer spines on the stems [11]. Figure 1 shows the photographs of different parts of P. bleo and P. grandifolia. Although they are different species, anatomical similarities in these two species support the evolution theory for cactus family [18].

Figure 1: Photographs of different plant parts of P. bleo and P. grandifolia. (a) Flower of P. bleo, (b) lower of P. grandifolia [47], (c) stem and spines of P. bleo, (d) stem and spines of P. grandifolia [48], (e) ripe fruits and seeds of P. bleo, and (f) ripe fruits and seeds of P. grandifolia [49].
3.2. Traditional Usage

P. bleo has been used for various purposes. In some areas, it is used as a food spice [1, 7]. This plant has been eaten raw as vegetables by some people in Malaysia and China or taken as a concoction brewed from fresh leaves [19, 36]. In addition, it is taken for detoxification and revitalizing the body [27, 28, 40]. Its fruit is consumed by some ethnic groups in Panama as a wild fruit [26]. The leaves of P. bleo have been traditionally used to treat cancer, hemorrhoid, hypertension, diabetes [32, 40], infections, gastric pain, headache, ulcer, and inflammatory conditions like rheumatism and asthma [28, 31]. Indigenous Colombians have used P. bleo to neutralize the effects of snakebites [33], to relax spastic muscles, and to alleviate muscle aches [29]. Apart from dietary and medicinal uses, this plant is a suitable barrier hedge because of its sharp spines, strong stem, and insect repellant properties [21]. In Central America, Kuna Indians used the crushed leaves to clarify drinking water [12]. Different methods of preparation have been reported for the plant. It is usually taken raw or as a decoction of its fresh leaves. Table 3 shows the traditional usage and different preparation methods of P. bleo. To the best of our knowledge, information on the specific preparation methods for some of the indicated traditional usages is not available.

Table 3: Traditional usage and methods of preparation of P. bleo.
3.3. Phytochemistry

The leaves are the most commonly used part of P. bleo in traditional medicine. Hence, they have been more studied compared to the other plant parts. So far, 20 phytoconstituents have been reported in the leaves and two components from the fruit as shown in Table 4. These components include alkaloids, fatty acids, glycosides, lactones, phenolic, sterol, terpenoid, and carotenoid compounds. The major isolated component from P. bleo leaves is phytol [27]. In addition, Doetsch et al. [34] reported the isolation of three alkaloids, namely, 3,4-dimethoxy-β-phenethylamine (mescaline), 3-methoxytyramine, and tyramine, from the leaves of this plant. Vitamin E (α-tocopherol) [36, 37] which is well known for its antioxidant properties; 2,4-ditert-butylphenol and dihydroactinidiolide were isolated through bioassay-guided fractionation by Malek et al. [36]. Murillo et al. [26] analyzed the fruit of P. bleo for lutein and zeaxanthin contents. The total carotenoid content of the fruit was found to be 13.3 μg/g, making P. bleo fruit a high carotenoid food source among the wild fruits in Panama.

Table 4: Reported phytoconstituents in the leaves and fruits of P. bleo.

The mineral content of the leaves was also investigated by using energy-dispersive X-ray microanalysis. Table 5 shows the weight percentage of the minerals reported by Abbdewahab et al. [38]. As can be seen, P. bleo leaves are rich in potassium (10.16%). This is more than two times of the potassium content of tomato (4.5%), a vegetable known to be high in potassium [50]. It has been shown that a high potassium diet has an important role in lowering blood pressure [51]. Therefore, it might be one of the possible reasons for the traditional usage of P. bleo as a treatment for hypertension [31].

Table 5: Percentage (% w/w) of mineral contents in the leaves of P. bleo [38].
3.4. Pharmacological Properties

Pharmacological evaluation of plants is based on their traditional uses. Cancer is one of the main causes of mortality and morbidity. Since P. bleo is traditionally used to prevent and treat cancer [28, 30, 40], it has been most studied for its antiproliferative and cancer protective properties [8, 22, 28, 32, 36, 39, 40]. This is followed by investigations of its antimicrobial and antiparasitic effects in vitro [8, 38, 4143, 52]. The snake venom neutralizing properties [33], antinociceptive effects [35], and toxicity [22, 31] of this plant have been evaluated through in vivo studies.

3.4.1. Antiproliferative Properties

The effects of different P. bleo extracts have been reported on various cell lines in vitro. The crude methanol extract and its ethyl acetate fraction had significant cytotoxic effects against human nasopharyngeal epidermoid carcinoma cell line (KB) [36]. In addition, the ethyl acetate fraction was more active than the methanol extract against human colon carcinoma (HCT116) and hormone dependent breast carcinoma cell lines (MCF7) [36]. Table 6 shows the reported IC50 values (μg/mL) for the antiproliferative effects of P. bleo extracts and fractions.

Table 6: IC50 values (g/mL) of P. bleo leaf extracts and fractions on different cell lines.

Gupta et al. [22] reported high tumor inhibition activity in “potato disc inhibition assay” using crown gall tumors (LC50 77 ppm). Their result was accompanied by a significant DNA peak reduction in the DNA intercalation test for the methanol extract of the whole plant.

To date, no report is available on the in vivo antiproliferative activities of P. bleo.

(1) Cytotoxic Components. Some of the cytotoxic components in P. bleo have been reported. Table 7 shows the reported IC50 (μg/mL) values of these components in the different human cell lines. The effects of these compounds and the mixture of the isolated sterols were not as high as doxorubicin, that is, a chemotherapy drug [28]. In another study, phytol isolated from P. bleo leaves was found to have a significant antitumor activity against some mouse cancer cell lines [36].

Table 7: Reported IC50 values (g/mL) of selected P. bleo phytoconstituents on human cell lines [28].

(2) Proposed Antiproliferative Mechanism. The antiproliferative activity of the methanol extract of P. bleo against human breast carcinoma cell line (T-47D) was found to be apoptotic in nature through the activation of caspase-3 and c-myc pathways [40]. Caspase-3 and c-myc are frequently activated death proteases which catalyze the specific cleavage of many key cellular proteins. They are also essential for normal development of the tissues as well as apoptosis in the tissues and cell types [53]. Komiya et al. [54] reported the induction of apoptosis as a mechanism of action for cytotoxic activity of phytol. DNA intercalation is another proposed mechanism of antiproliferative activity for P. bleo [22]. However, in some studies, P. bleo did not show appreciable cytotoxic effect [32]. Differences in the sources of plants, extraction methods, assay methods, and cell lines can be the possible reasons for these discrepancies. On the other hand, P. bleo may contain some prodrugs which are metabolized to the active metabolites. Therefore, further studies are needed to better understand its antiproliferative activity.

Apart from the cytotoxic activities against cancer cell lines, crude methanol extract and its fractions (hexane, water, and ethyl acetate) did not show any cytotoxicity to the normal human fibroblast cell lines, MRC-5 [36].

3.4.2. Antioxidant Activity

The adverse effects of oxidative stress on human health have become a serious issue. Oxidative stress causes production of free radicals in the body that facilitate the development of degenerative diseases such as cardiovascular diseases, cancers, neurodegenerative disorders [55], Alzheimer’s, and inflammatory diseases [56]. One solution to this problem is to supplement the diet with antioxidant compounds found in natural plant sources [57]. Hence, in the literature, the antioxidant effects of P. bleo were evaluated using different assays as follows.

2,2-Diphenyl-1-picrylhydrazyl Hydrate (DPPH) Assay. The methanol, dichloromethane, ethyl acetate, and hexane extracts of P. bleo leaves were tested [8, 25]. The hexane extract exhibited the most effective radical scavenging activity (EC50 210 μg/mL) followed by the ethyl acetate extract (EC50 225 μg/mL). This spectrophotometric assay uses a stable radical 2,2′-diphenylpicrylhydrazyl (DPPH) as a reagent [8, 25].

Ferric Reducing Antioxidant Potential Assay (FRAP). The hexane, water, and methanol extracts of P. bleo leaves were found to reduce Fe3+/ferric cyanide complex to the ferrous form. Although the reduction was statistically significant, it was not more than ascorbic acid (vitamin C) and butylated hydroxyanisole (BHA) as positive controls [25]. Hassanbaglou et al. [37] compared the antioxidant activity of the ethyl acetate extract with that of hexane, ethanol, and methanol extracts. They showed that the ethyl acetate extract had significantly higher antioxidant properties compared to the rest of the tested extracts. FRAP measures the ability of test samples to reduce ferric ion to the ferrous form of TPTZ (2,4,6-tripyridyl-s-triazine).

β-Carotene-Linoleic Bleaching Assay. The ethyl acetate extract of P. bleo demonstrated the strongest antioxidant activity followed by the methanol extract reported by Sim et al. [25]. In this assay, the linoleate free radicals formed during the reaction are neutralized by antioxidants.

In general, although different studies used plant materials from different sources and nonsimilar extraction methods, ethyl acetate and hexane extracts appear to be the strongest antioxidant extracts from the P. bleo leaves [8, 25, 37]. Moreover, this antioxidant capacity is strongly associated with the total phenolic compounds and flavonoid content of the plant leaves [25, 37, 58]. The above studies suggest that P. bleo has antioxidant properties which can be one of the possible reasons for its traditional usage for detoxification and prevention of cancer.

3.4.3. Antimicrobial Properties

P. bleo has been shown to possess antibacterial, antiviral, and antifungal properties in vitro. Table 8 shows the effect of P. bleo extracts on selected bacteria and fungi. As can be seen, the methanol and hexane extracts demonstrated great antibacterial activities against Salmonella choleraesuis and Pseudomonas aeruginosa. In addition, its dichloromethane extract showed promising antibacterial effect against Methicillin resistant Staphylococcus aureus [8, 38]. All of the mentioned bacteria are among the main causes of nosocomial infections and they have been developing antibiotic resistance [5961]. Therefore, the potential antibacterial activity of P. bleo needs to be further investigated to identify the lead(s) antibacterial component(s).

Table 8: Reported effects of P. bleo extracts on the growth of selected bacteria and fungi.

The antifungal activity of the water and methanol extract of P. bleo leaves against Cladosporium cucumerinum, a plant pathogenic fungus, has been reported [43], but they were not active against Candida albicans, a common human pathogen [42, 43].

The antiviral properties of the water and methanol extracts of P. bleo leaves were evaluated against Herpes Simplex Virus-I (HSV-1) and Human Immunodeficiency Virus (HIV) by Matsuse et al. [62]. Both of the extracts demonstrated anti-HIV activity. However, the result of this study was not promising because of the low selectivity index of 0.94. Besides, in another study by Hattori et al. [63], the same extracts did not demonstrate any antiviral activity against HSV-1. In general, the available data on the antiviral activity of P. bleo is neither sufficient nor conclusive. Therefore, further research needs to be carried out.

3.4.4. Antiparasitic Properties

The only antiparasitic investigation on P. bleo was reported by Marston et al. [52]. In their study, the chloroform, methanol, and water extracts of this plant did not exert any antiparasitic activity against schistosomiasis.

3.4.5. Neutralizing Snake Venom

Otero et al. [33] evaluated the neutralizing effect of the ethanol extract of P. bleo on hemorrhagic activity of “Bothrops atrox venom” in mice. This extract did not show any neutralizing effect against the tested venom.

3.4.6. Antinociceptive Properties

Wahab et al. [35] evaluated the antinociceptive activity of the ethanol extract and its fractions using two in vivo analgesic models: peripheral formalin-induced licking and acetic acid-induced abdominal writhing. They showed that the ethanol extract, hexane fraction, dichloromethane fraction, and ethyl acetate fraction of P. bleo had moderate antinociceptive effects. However, no compound was identified in their study.

3.5. Toxicity Studies

Acute toxicity effect of the leave’s extracts of P. bleo was evaluated by in vitro and in vivo studies. Er et al. [32] showed that the water extract may form mutagenic compound(s) upon metabolization by the liver enzymes in vitro. In another study by Gupta et al. [22], the methanol extract of the whole plant had moderate toxicity in brine shrimp toxicity assay (LD50 77 ppm). In the only in vivo study by Sim et al. [31], the methanol extract did not have any toxicity effect on ICR mice (LD50 > 2500 mg/kg). Although animal models have around 70–80% predictability for human toxicities [64, 65], the long term toxicity and the mutagenicity of metabolites of P. bleo should be further investigated.

4. Conclusion

A comprehensive review on Pereskia bleo has been presented. It provides an overview of the botanical characteristics, traditional usage, phytoconstituents, pharmacological activities, and safety of P. bleo. The current review highlights the association between the traditional usage of the plant and the reported anticancer, antibacterial, and antinociceptive effects tested in different studies. Although P. bleo has been traditionally used for a variety of therapeutic and prophylactic purposes, only a few of them has been investigated. Hence, more research is warranted to further study its biological activities and chemical properties to understand its traditional usage and to develop novel therapeutics. Understanding the traditional uses, knowing the available scientific evidences, and identifying the gaps in research will allow the proper translation of promising research results into a safe and efficacious usage of herbal medicine and discovery of new therapeutics. It will also assist in setting appropriate policy and guidelines in the usage of herbal medicine.

Conflict of Interests

All authors declare that there is no conflict of interests regarding the publication of this paper.


Funding from the National University of Singapore (NUS) research Grant (R-148-000-137-112 to KHL) and Leeward Pacific Pte Ltd. (R-148-000-140-592 to KHL) and research scholarship from the Singapore International Graduate Award (SINGA, SZ) are acknowledged.


  1. C. Wiart, Medicinal Plants of Asia and the Pacific: Drugs of the Future, World Scientific, Singapore, 2006.
  2. N. L. Britton and J. N. Rose, The Cactaceae, Descriptions and Illustrations of Plants of the Cactus Family, Dover Publications, Washington, DC, USA, 2009.
  3. E. J. Edwards and M. J. Donoghue, “Pereskia and the origin of the cactus life-form,” American Naturalist, vol. 167, no. 6, pp. 777–793, 2006. View at Publisher · View at Google Scholar · View at Scopus
  4. E. J. Edwards, R. Nyffeler, and M. J. Donoghue, “Basal cactus phylogeny: implications of Pereskia (Cactaceae) paraphyly for the transition to the cactus life form,” American Journal of Botany, vol. 92, no. 7, pp. 1177–1188, 2005. View at Google Scholar · View at Scopus
  5. R. M. Ogburn and E. J. Edwards, “Anatomical variation in Cactaceae and relatives: trait lability and evolutionary innovation,” American Journal of Botany, vol. 96, no. 2, pp. 391–408, 2009. View at Publisher · View at Google Scholar · View at Scopus
  6. C. M. Boo, C. L. Ou-Yang, and K. Omar-Hor, 1001 Garden Plants in Singapore, National Parks Board, Singapore, 2nd edition, 2007.
  7. Singapore Npark Board, NParks Flora&Founa web, 2010, https://florafaunaweb.nparks.gov.sg/Special-Pages/plant-detail.aspx?id=2324#.
  8. S. I. A. Wahab, A. B. Abdul, S. M. Mohan, A. S. Al-Zubairi, M. M. Elhassan, and M. Y. Ibrahim, “Biological activities of Pereskia bleo extracts,” International Journal of Pharmacology, vol. 5, no. 1, pp. 71–75, 2009. View at Publisher · View at Google Scholar · View at Scopus
  9. R. T. Bárcenas, C. Yesson, and J. A. Hawkins, “Molecular systematics of the Cactaceae,” Cladistics, vol. 27, no. 5, pp. 470–489, 2011. View at Publisher · View at Google Scholar · View at Scopus
  10. K. Y. Chong, H. T. Tan, and R. T. Corlett, A Checklist of the Total Vascular Plant Flora of Singapore: Native, Naturalised and Cultivated Species, Raffles Museum of Biodiversity Research, National University of Singapore, Singapore, 2009, http://rmbr.nus.edu.sg/raffles_museum_pub/flora_of_singapore_tc.pdf.
  11. A. M. Sri Nurestri, K. S. Sim, and A. W. Norhanom, “Phytochemical and cytotoxic investigations of Pereskia grandifolia Haw. (Cactaceae) leaves,” Journal of Biological Sciences, vol. 9, no. 5, pp. 488–493, 2009. View at Publisher · View at Google Scholar · View at Scopus
  12. E. Anderson, The Cactus Family, pp. 566–568, Timber Press, Puritana, Ore, USA, 1st edition, 2001.
  13. R. P. Wunderlin and B. F. Hansen, “Atlas of Florida Vascular Plants,” 2008, http://www.plantatlas.usf.edu/.
  14. N. P. Taylor, D. Zappi, P. Braun, and M. Machado, “Pereskia aculeata. Iucn Red List of Threatened Species. Version 2013. 2,” 2013, http://www.iucnredlist.org.
  15. E. Pooley, A Field Guide to Wild Flowers KwaZulu Natal and the Eastern Region, Natal Flora Publications Trust, Durban, South Africa, 1999.
  16. A. G. I. Natural Heritage Trust, “Weed Management Guide, Leaf cactus, Pereskia aculeata,” 2003, http://www.environment.gov.au/biodiversity/invasive/weeds/publications/guidelines/alert/pubs/p-aculeata.pdf.
  17. Tropicos, “Missouri Botanical Garden (MBG),” 2012, http://www.tropicos.org/Name/5100482.
  18. B. E. Leuenberger, “Pereskia, Maihuenia, and Blossfeldia-taxonomic history, updates, and notes,” Haseltonia, no. 14, pp. 54–93, 2008. View at Google Scholar · View at Scopus
  19. J. Nugent, “Permaculture Plants, agaves and cacti,” 2007, http://books.google.com.sg/books?id=YVwMM2OdO34C&q=Pereskia+bleo#v=snippet&q=Pereskia%20bleo&f=false.
  20. B. E. Leuenberger, “Humboldt & Bonpland's Cactaceae in the herbaria at Paris and Berlin,” Willdenowia, vol. 32, pp. 137–153, 2002. View at Google Scholar
  21. K. A. Liamas, Tropical Flowering Plants: A Guide to Identification and Cultivation, Timber Press, Portland, Ore, USA, 2003.
  22. M. P. Gupta, A. Monge, G. A. Karikas et al., “Screening of Panamanian medicinal plants for brine shrimp toxicity, crown gall tumor inhibition, cytotoxicity and DNA intercalation,” Pharmaceutical Biology, vol. 34, no. 1, pp. 19–27, 1996. View at Google Scholar
  23. C. C. Kazama, D. T. Uchida, K. N. Canzi et al., “Involvement of arginine-vasopressin in the diuretic and hypotensive effects of Pereskia grandifolia Haw. (Cactaceae),” Journal of Ethnopharmacology, vol. 144, no. 1, pp. 86–93, 2012. View at Google Scholar
  24. USDA, “National Genetic Resources Program, Germplasm Resources Information Network—(GRIN),” [Online Database], 2012, http://www.ars-grin.gov/cgi-bin/npgs/html/tax_search.pl?Pereskia+bleo%.
  25. K. S. Sim, A. M. Sri Nurestri, and A. W. Norhanom, “Phenolic content and antioxidant activity of crude and fractionated extracts of Pereskia bleo (Kunth) DC. (Cactaceae),” African Journal of Pharmacy and Pharmacology, vol. 4, no. 5, pp. 193–201, 2010. View at Google Scholar · View at Scopus
  26. E. Murillo, A. J. Meléndez-Martínez, and F. Portugal, “Screening of vegetables and fruits from Panama for rich sources of lutein and zeaxanthin,” Food Chemistry, vol. 122, no. 1, pp. 167–172, 2010. View at Publisher · View at Google Scholar · View at Scopus
  27. K. Hostettmann, A. Marston, M. Maillard, and M. Hamburger, Phytochemistry of Plants Used in Traditional Medicine, pp. 373–376, Oxford University Press, Oxford, UK, 1995.
  28. S. N. A. Malek, S. K. Shin, N. A. Wahab, and H. Yaacob, “Cytotoxic components of Pereskia bleo (Kunth) DC. (Cactaceae) leaves,” Molecules, vol. 14, no. 5, pp. 1713–1724, 2009. View at Publisher · View at Google Scholar · View at Scopus
  29. M. P. Gupta, A. Correa, D. Mireya et al., “Medicinal plant inventory of Kuna Indians: part 1,” Journal of Ethnopharmacology, vol. 40, no. 2, pp. 77–109, 1993. View at Publisher · View at Google Scholar · View at Scopus
  30. A. Rahmat, F. P. Saib, and N. A. Buslima, “Comparing the effect of ficus benjamina extract and Pereskia saecnarosa extract on tthe level of micro and macro minerals in normal and induced liver cancer rats,” in Proceedings of the 4th International Conference on Biomedical Engineering in Vietnam, pp. 208–212, 1980.
  31. K. S. Sim, A. M. Sri Nurestri, S. K. Sinniah, K. H. Kim, and A. W. Norhanom, “Acute oral toxicity of Pereskia bleo and Pereskia grandifolia in mice,” Pharmacognosy Magazine, vol. 6, no. 21, pp. 67–70, 2010. View at Publisher · View at Google Scholar · View at Scopus
  32. H. M. Er, E. Cheng, and A. K. Radhakrishnan, “Anti-proliferative and mutagenic activities of aqueous and methanol extracts of leaves from Pereskia bleo (Kunth) DC (Cactaceae),” Journal of Ethnopharmacology, vol. 113, no. 3, pp. 448–456, 2007. View at Publisher · View at Google Scholar · View at Scopus
  33. R. Otero, V. Núñez, J. Barona et al., “Snakebites and ethnobotany in the northwest region of Colombia, part III: neutralization of the haemorrhagic effect of Bothrops atrox venom,” Journal of Ethnopharmacology, vol. 73, no. 1-2, pp. 233–241, 2000. View at Publisher · View at Google Scholar · View at Scopus
  34. P. W. Doetsch, J. M. Cassady, and J. L. McLaughlin, “Cactus alkaloids: XL. Identification of mescaline and other β-phenethylamines in Pereskia, Pereskiopsis and Islaya by use of fluorescamine conjugates,” Journal of Chromatography A, vol. 189, no. 1, pp. 79–85, 1980. View at Google Scholar · View at Scopus
  35. I. R. A. Wahab, C. C. Guilhon, P. D. Fernandes, and F. Boylan, “Anti-nociceptive activity of Pereskia bleo Kunth. (Cactaceae) leaves extracts,” Journal of Ethnopharmacology, vol. 144, no. 3, pp. 741–746, 2012. View at Google Scholar
  36. S. N. A. Malek, N. A. Wahab, H. Yaacob et al., “Cytotoxic activity of Pereskia bleo (Cactaceae) against selected human cell lines,” International Journal of Cancer Research, vol. 4, no. 1, pp. 20–27, 2008. View at Google Scholar · View at Scopus
  37. B. Hassanbaglou, A. A. Hamid, A. Roheeyati et al., “Antioxidant activity of different extracts from leaves of Pereskia bleo (Cactaceae),” Journal of Meidinal Plants Research, vol. 6, no. 15, pp. 2932–2937, 2012. View at Google Scholar
  38. S. I. Abbdewahab, N. M. Ain, A. B. Abdul, M. M. E. Taha, and T. A. T. Ibrahim, “Energy-dispersive X-ray microanalysis of elements' content and antimicrobial properties of Pereskia bleo and Goniothalamus umbrosus,” African Journal of Biotechnology, vol. 8, no. 10, pp. 2375–2378, 2009. View at Google Scholar · View at Scopus
  39. S. Y. Liew, E. J. Stanbridge, K. Yusoff, and N. Shafee, “Hypoxia affects cellular responses to plant extracts,” Journal of Ethnopharmacology, vol. 144, no. 2, pp. 453–456, 2012. View at Google Scholar
  40. M. L. Tan, S. F. Sulaiman, N. Najimuddin, M. R. Samian, and T. S. T. Muhammad, “Methanolic extract of Pereskia bleo (Kunth) DC. (Cactaceae) induces apoptosis in breast carcinoma, T47-D cell line,” Journal of Ethnopharmacology, vol. 96, no. 1-2, pp. 287–294, 2005. View at Publisher · View at Google Scholar · View at Scopus
  41. K. Philip, S. N. A. Malek, W. Sani et al., “Antimicrobial activity of some medicinal plants from Malaysia,” American Journal of Applied Sciences, vol. 6, no. 8, pp. 1613–1617, 2009. View at Publisher · View at Google Scholar · View at Scopus
  42. T. Rüegg, A. I. Calderón, E. F. Queiroz et al., “3-farnesyl-2-hydroxybenzoic acid is a new anti-Helicobacter pylori compound from Piper multiplinervium,” Journal of Ethnopharmacology, vol. 103, no. 3, pp. 461–467, 2006. View at Publisher · View at Google Scholar · View at Scopus
  43. L. Rahalison, M. Hamburger, K. Hostettmann et al., “Screening for antifungal activity of Panamanian plants,” International Journal of Pharmacognosy, vol. 31, no. 1, pp. 68–76, 1993. View at Google Scholar · View at Scopus
  44. A. P. D. Candolle, “Pereskia bleo (Kunth) DC,” 2011, http://www.tropicos.org/Name/5100482.
  45. USDA, “Taxon: Pereskia bleo,” 2013, http://www.ars-grin.gov/cgi-bin/npgs/html/tax_search.pl?Pereskia+bleo%.
  46. IPNI, “International Plant Names Index,” 2005, http://www.ipni.org/ipni/plantNameByVersion.do?id=273592-2&version=1.3.
  47. M. Gardener, “Tropical plants library online,” 2014, http://mgonline.com/articles/exotics.aspx.
  48. S. Kurt, “Stem of P. grandifolia,” 2014, http://www.biolib.de/.
  49. NRCS, “Natural Resources and Conservation Service of USDA, Plant profile of P. grandifolia Haw,” 2013, http://plants.usda.gov/core/profile?symbol=PEGR14#.
  50. D. C. Sanders, A. S. Grayson, and T. J. Monaco, “Mineral content of tomato (Lycopersicon esculentum) and four competing weed species,” Weed Science, vol. 29, no. 5, pp. 590–593, 1981. View at Google Scholar
  51. J. M. Geleijnse, J. C. Witteman, A. A. Bak, J. H. den Breeijen, and D. E. Grobbee, “Reduction in blood pressure with a low sodium, high potassium, high magnesium salt in older subjects with mild to moderate hypertension,” British Medical Journal, vol. 309, no. 6952, pp. 436–440, 1994. View at Google Scholar · View at Scopus
  52. A. Marston, G. Dudan, M. P. Gupta, P. N. Solis, M. D. Correa, and K. Hostettmann, “Screening of Panamanian plants for molluscicidal activity,” Pharmaceutical Biology, vol. 34, no. 1, pp. 15–18, 1996. View at Google Scholar
  53. A. G. Porter and R. U. Jänicke, “Emerging roles of caspase-3 in apoptosis,” Cell Death and Differentiation, vol. 6, no. 2, pp. 99–104, 1999. View at Google Scholar · View at Scopus
  54. T. Komiya, M. Kyohkon, S. Ohwaki et al., “Phytol induces programmed cell death in human lymphoid leukemia Molt 4B cells,” International Journal of Molecular Medicine, vol. 4, no. 4, pp. 377–380, 1999. View at Google Scholar · View at Scopus
  55. M. Gerber, M. C. Boutron-Ruault, S. Hercberg, E. Riboli, A. Scalbert, and M. H. Siess, “Food and cancer: state of the art about the protective effect of fruits and vegetables,” Bulletin du Cancer, vol. 89, no. 3, pp. 293–312, 2002. View at Google Scholar · View at Scopus
  56. V. di Matteo and E. Esposito, “Biochemical and therapeutic effects of antioxidants in the treatment of Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis,” Current Drug Targets-CNS & Neurological Disorders, vol. 2, no. 2, pp. 95–107, 2003. View at Google Scholar · View at Scopus
  57. P. Knekt, R. Jarvinen, A. Reunanen, and J. Maatela, “Flavonoid intake and coronary mortality in Finland: a cohort study,” British Medical Journal, vol. 312, no. 7029, pp. 478–481, 1996. View at Google Scholar
  58. R. A. Mustafa, A. Abdul Hamid, S. Mohamed, and F. A. Bakar, “Total phenolic compounds, flavonoids, and radical scavenging activity of 21 selected tropical plants,” Journal of Food Science, vol. 75, no. 1, pp. C28–C35, 2010. View at Publisher · View at Google Scholar · View at Scopus
  59. E. B. Breidenstein, C. de la Fuente-Núñez, and R. E. Hancock, “Pseudomonas aeruginosa: all roads lead to resistance,” Trends in Microbiology, vol. 19, no. 8, pp. 419–426, 2011. View at Publisher · View at Google Scholar · View at Scopus
  60. C. Chu, C.-H. Chiu, W.-Y. Wu, C.-H. Chu, T.-P. Liu, and J. T. Ou, “Large drug resistance virulence plasmids of clinical isolates of Salmonella enterica serovar Choleraesuis,” Antimicrobial Agents and Chemotherapy, vol. 45, no. 8, pp. 2299–2303, 2001. View at Publisher · View at Google Scholar · View at Scopus
  61. K. Hiramatsu, H. Hanaki, T. Ino, K. Yabuta, T. Oguri, and F. Tenover, “Methicillin-resistant Staphylococcus aureus clinical strain with reduced vancomycin susceptibility,” Journal of Antimicrobial Chemotherapy, vol. 40, no. 1, pp. 135–136, 1997. View at Google Scholar
  62. I. T. Matsuse, Y. A. Lim, M. Hattori, M. Correa, and M. P. Gupta, “A search for anti-viral properties in Panamanian medicinal plants: the effects on HIV and its essential enzymes,” Journal of Ethnopharmacology, vol. 64, no. 1, pp. 15–22, 1998. View at Publisher · View at Google Scholar · View at Scopus
  63. M. Hattori, T. Nakabayashi, Y. A. Lim et al., “Inhibitory effects of various Ayurvedic and Panamanian medicinal plants on the infection of herpes simplex virus-1 in vitro and in vivo,” Phytotherapy Research, vol. 9, no. 4, pp. 270–276, 1995. View at Publisher · View at Google Scholar · View at Scopus
  64. I. Kola and J. Landis, “Can the pharmaceutical industry reduce attrition rates?” Nature Reviews Drug Discovery, vol. 3, no. 8, pp. 711–716, 2004. View at Google Scholar · View at Scopus
  65. H. Olson, G. Betton, D. Robinson et al., “Concordance of the toxicity of pharmaceuticals in humans and in animals,” Regulatory Toxicology and Pharmacology, vol. 32, no. 1, pp. 56–67, 2000. View at Publisher · View at Google Scholar · View at Scopus