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Review Article

A Review About Barleria Prionitis; A Rare Known Shrub with Potential Medicinal Properties

Sameena Farrukh*

Corresponding Author: Sameena Farrukh Department of Education and Research, NITTTR, Bhopal, India.

Received: March 19, 2022 ;    Revised: April 6, 2022 ;    Accepted: April 9, 2022 ;   Available Online: May 1, 2022

Citation: Farrukh S. (2022) A Review About Barleria Prionitis; A Rare Known Shrub with Potential Medicinal Properties. J Pharm Sci Drug Discov, 1(1): 1-7.

Copyrights: ©2022 Farrukh S. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

There are thousands of species which are known for their potential medicinal properties while many of them are still need to be discovered as a potential drug targets and their active drug molecules. B. prionitis is one of the rarely known shrubs which has wonderful medicinal properties whether its leaves, flowers, stem and whole plant. It is native to tropical East Africa and tropical and temperate Asia. The whole plant leaves, and roots are used for a variety of purposes in traditional Indian medicine. For example, the leaves are used to promote healing of wounds and to relieve joint pains and toothache. Because of its antiseptic properties, extracts of the plant are incorporated into herbal cosmetics and hair products to promote skin and scalp health. Preliminary phytochemical analysis of hydro-methanol of B. prionitis whole plant indicated the presence of glycosides, saponins, flavonoids, steroids and tannins. The antidiabetic activity of alcoholic extract of leaf and root of B. prionitis was evaluated by using alloxan monohydrate. B. prionitis leaves showed significant decrease in blood glucose level, glycosylated hemoglobulin and significant increase in serum insulin and liver glycogen level. B. prionitis root showed moderate but non-significant anti-diabetic activity in experimental animals.

Keywords: Barleria Prionitis. Drug, Phytochemistry, Traditional medicine

INTRODUCTION

From the time immortal plants always has been used as food and medicines. There are thousands of species which are known for their potential medicinal properties while many of them are still need to be discovered as a potential drug targets and their active drug molecules. India is not only known for its broad diverse culture and tradition but also known for its broad diversity of plant species because of diversified landscaping and varied climates.  During the last decade, use of traditional medicine has expanded globally and gained popularity. Because of awareness of deleterious effects of modern synthetic drugs, the plant-based drugs are getting much attention for use in herbal medicines, antioxidants and cosmetics. Natural products have a significant role in pharmaceutical industry as potential drug sources and bio active compounds [1].

In English it is commonly known as: Barleria, porcupine-flower, Common yellow nail dye, Thorn nails dye, Yellow Hedge Barleria (Barleria acanthoides is known as Vajradanti, Spiny White barleria; Barleria cristata L. is known as Jhinti, Kurabaka, Sahachara, Sahacharah, Crested purple nail dye, Philippine violet), German: Stachelschweinblume; Unani: Katsaraiya, Piyabaasa; Urdu: Pila Bansa, Piya Bansa; Hindi: झिण्टी jhinti, परुष parush, पीला पियाबांसा pila piyabansa, पीली कटसरैया pili katsaraiya, वज्रदंती vajradanti; Bengali: kantajhinti; Kannada: haladi gorate, kurantaka, madarangi gida, mullugoranta; Konkani: कोरांटी koranti; Malayalam: chemmulli, Manjakanakambaram, mannakkanakambaram; Sanskrit: आर्तगलः artagalah, बाण bana, dasi kurantakah, झिण्टी jhinti, ककुभ kakubha, किङ्किरातः kinkiratah, कुरण्टकः kurantakah, कुरवकः kuravakah, महासह mahasaha, पीतसैरीयकः pitasairiyakah, सहचरः sahacharah, उद्यानपाकी udyanapaki, वज्रदन्ती vajradanti.

SCIENTIFIC CLASSIFICATION 

Kingdom:              Plantae

Subkingdom:         Tracheobionta

Division:                Magnoliophyta

Class:                    Magnoliopsida

Subclass:               Asteridae

Order:                   Scrophulariale

Genus:                   Barleria

Species:                 Prionitis

Botanical name:      Barleria prionitis

Family:                   Acanthaceae (Acanthus family)

Synonyms:             Barleria appressa, Barleria coriacea, Barleria spicata

Barleria Prionitis is an erect, prickly shrub, usually single-stemmed, growing to about 1.5 m tall. Spines are about 1.2 cm long. Leaves are up to 5-9 x 2.5-4 cm, elliptic, pointed, with a fine point, base wedge-shaped, sparsely puberulus, fringed with hairs on the margins, gland dotted beneath, leaf-stalk up to 2 cm. Orange-yellow flowers are borne in cymes in leaf-axils; bracts 2, 1.5 cm, oblong with a fine point at the tip. Outer sepals are 1.3 x 0.4 cm, inner 1.1 x 0.2 cm, fine-tipped, hairy. Flower tube is 2.5 cm, petals 2 cm obovate, filaments 1.3 cm, staminodes 2, remaining at the base of the flower tube. Ovary is 2.5 mm, style 2.5 cm [4].

In South Africa, B. prionitis is pollinated by insects and attracts various species of butterflies [4]. In Puerto Rico it flowers from September to December and fruits are produced from January to April [5]. In China, it has been recorded flowering from October to December and fruiting from December to February.

B. prionitis grows in a wide variety of soils, but it grows best in well-drained sandy soils. Within its naturalized range, for example in Puerto Rico, it grows in areas receiving from about 750-900 mm of mean annual precipitation [3]. B. prionitis is moderately intolerant of shade, growing in both full sunlight and under light forest canopies [6].

MEDICINAL USES

Porcupine Flower has numerous medicinal properties including treating fever, respiratory diseases, toothache, joint pains and a variety of other ailments; and it has several cosmetic uses. A mouthwash made from root tissue is used to relieve toothache and treat bleeding gums. The whole plant leaves, and roots are used for a variety of purposes in traditional Indian medicine. For example, the leaves are used to promote healing of wounds and to relieve joint pains and toothache. Because of its antiseptic properties, extracts of the plant are incorporated into herbal cosmetics and hair products to promote skin and scalp health. It used in Indonesia as a component in traditional medicines [7], parts of the plant are bitter, astringent in taste, and are regarded in Myanmar as highly beneficial for skin, blood and other diseases [8]. Often combined with sesame oil and fermented-rice washing-water, the whole plant, leaves (sometimes burnt to ash or crushed for juice), stems, branches, and roots are used together or separately. In Pakistan shrubs are grown as a hedge while its bitter quinine-like extract is used in traditional medicine to treat whooping cough and tuberculosis [9].

Author itself has undergone to Case studies at father’s own homeopathic clinic (Homeopathic practitioner), for treating Renal stones with the leaves of ‘B. Prionitis’ as ‘traditional medicine’ considering its amazing diuretic properties, more than 30 cases of patients undertaken for studies suffering from renal stones who were treated at different intervals. As the size of stone varied from patient to patient ranging from 10mm to 30mm. The patients were advised to take paste of three leaves orally, following with a glass of butter milk before going to bed for 3 days.

Observations were as follows:

  • 70% percent of patients got relief within three days.
  • 30% were asked to repeat the medication with interval of 15 days and they got relief.

(A detailed statistical report is in process and will be presented in next research article)

Traditional Uses (Table 1)

CHEMICAL CONSTITUENTS

The Barleria prionitis leaves and flowering tops are reported to rich in potassium salt [21]. Preliminary phytochemical analysis of hydromethanolic extract of B. prionitis whole plant indicated presence of flavonoid, glycoside, saponin, tannins and steroid [22]. Phytochemicals isolated from B. prionitis such as balarenone, pipataline, lupeol, prioniside A and Prioniside B [23]. Glycoside are isolated from the areal plant are barlerinoside, verbascoside, shanzhiside methyl ester, 6-0-trans-p-coumaroyl-8-o-acetylshanzhiside methyl ester, barlerin, acetylbarlerin and 7- methoxy diderroside. Chromatographic examination of the alcoholic extract of the leaves and stems of Barleria prionitis Linn, revealed the presence of iridinoid glycosides such as acetyl barlerin and barlerin [9,21,15]. The leaves were reported to contain scutellarein, melilotic acid, synergic acid and 6-hydroxyflavones [24]. β-sitosterol, scutellarein 7- neohesperidoside and apigenine 7-O-glucoside are present in B. Prionitis. Two new anthraquinones compound isolated from Barleria prionitis and characterized as 1,8, dihydroxy-2,7-dimethyl 3,6-dimethoxy anthraquinone,1,3,6,8-tetra methoxy-2,7-dimethyl anthraquinone.

PHYTOCHEMISTRY

Preliminary phytochemical analysis of hydro-methanolic extract of B. prionitis whole plant indicated the presence of glycosides, saponins, flavonoids, steroids and tannins [25]. The leaves and flowering tops were reported to rich in potassium salts [5]. Several phytochemicals viz., balarenone (1), pipataline (2), lupeol (3), prioniside A (4), prioniside B (5) and prioniside C (6) has been isolated from the ethanolic extract of B. prionitis [10]. Numbers of glycosides include barlerinoside (7), verbascoside (8), shanzhiside methyl ester (9), 6-O-trans-p-coumaroyl-8-O-acetylshanzhiside methyl ester (10), barlerin (11), acetylbarlerin (12), 7-methoxydiderroside (13), lupulinoside (14) has been also isolated from the aerial parts [10]. Two anthraquinones derivatives has been also identified in this plant and their structures were characterized as 1,8, dihydroxy-2,7-dimethyl 3, 6-dimethoxy anthraquinone and 1,3,6,8-tetra methoxy-2,7-dimethyl anthraquinone [26]. The leaves were reported to contain scutellarein (15), melilotic acid (16), syringic acid (17), vanillic acid (18), p-hydroxybenzoic acid (19), 6-hydroxyflavones (20) [5]. Beside these phytochemicals, luteolin-7-O-β-D-glucoside (21), β-sitosterol (22), scutellarein 7-neohesperidoside (23), apigenin 7-O-glucoside (24), 13, 14-seco-stigmasta-5, 14-diene-3-a-ol (25) were also reported to present in B. prionitis [27] (Figure 2).

Anti-Diabetic Activity

The antidiabetic activity of alcoholic extract of leaf and root of B. prionitis was evaluated by using alloxan monohydrate. B. prionitis leaves showed significant decrease in blood glucose level, glycosylated hemoglobulin and significant increase in serum insulin and liver glycogen level. B. prionitis root showed moderate but non-significant anti-diabetic activity in experimental animals [24].

Antidiarrheal Activity

Butanol fraction of B. prionitis leaves showed significant anti-diarrheal activity. In vivo study showed that the butanol fraction dose dependently inhibited the castor oil induced diarrhea and PGE2 induced enter pooling in sprague-dawley rats. The butanol fraction also reduced the gastrointestinal motility in response to charcoal-induced gut transit changes [21].

Diuretic Activity

Diuretic activity of B. prionitis flower extract was investigated using by administration of normal saline solution. Administration of aqueous flower extract was significantly increased the urination and sodium elimination but not potassium in rats. The diuretic effect of flower extract was comparable and significant with the reference drug furosemide [15].

Toxicity Studies

Alcoholic extract of roots and leaves oft of B. prionitis did not showed any toxic effect in adult albino rats. During the 14 days of study period death was not observed on oral administration of extract [30]. Using different dose of iridoid fraction in the safety evaluation and maximum tolerance dose study the oral LD50 with no signs of abnormalities or any mortality observed [31].

Gastro-Protective Activity

Maximum protections were found to be 66.26%and 59.42% by iridoid fraction (200 mg/kg) in PL induced ulcer and CRS-induced ulcer rat model. Iridoid fraction from leaves reduced ulcer index [21]. In ethanol induced gastric ulcer rat model, methanolic extract of leaf (500 mg/kg bw) and ranitidine provided 67.7and 75.5% inhibition of ulcer. Same dose of extract and drug displayed 70.3 and 62.2% inhibition in indomethacin induced gastric ulcers model. Extract also showed efficacy against indomethacin induced gastric mucosal damage and increased liver enzymes in ethanol induced ulcer rat model [30].

DISCUSSION

It is evident from different studies that B. Prionitis potentially carries medicinal properties and in India it has been traditionally used to cure various ailments. As per the studies of [10,11,14] refer (Table 1) leaves of B. Prionitis can be used to cure skin diseases, scabies, glandular swellings etc. if applied directly as paste or juice given orally (as mentioned specifically in Table 1). Similarly, according to the studies of [11,16] and other authors (Table 1) Stem, root flower and whole plant can be used to treat various diseases like viral fever, rheumatic fever whooping cough, Edema etc. In the present study author has mentioned the case studies of 30 patients getting relief from renal stones when they were advised to take a paste of leaves orally followed by glass of butter milk for 3 days in continuation and more than 70% patients got relief within fortnight. This proves its amazing diuretic property and other medicinal properties makes B. Prionitis a special medicinal plant while it is still merely known to common PR actioners and pharmacists as well.

Besides, the phytochemical analysis of various parts of the plant also indicated the presence of glycosides, saponins, flavonoids, steroids and tannins [25]. The leaves and flowering tops were reported to rich in potassium salts [18] and other important phytochemicals (Table 2) has been reported by different scientists.

Moreover, anti-diabetic activity, antidiarrheal activity, anti-toxicity and Gastro protective activities has also been mentioned when tested on rats by different workers as mentioned in above paragraphs.

Hence, present review about amazing medicinal properties of B. Prionitis as suggested and reported by various authors will be helpful to disseminate the knowledge among practitioners, pharmacists and other workers and opens a gateway for further studies on the basis of existing scientific reports.

CONCLUSION

In the present studies it has been found that B. Prionitis has tremendous medicinal properties and can be used as potential drug in various combinations to cure many diseases. Though it is a very commonly found herbal plant in almost every part of Asia but still its significant properties are rarely known and undiscovered. Hence further research is suggested to understand its pharmacological importance against numerous diseases and to identify its phytochemical metabolites. So that it can be used efficiently in pharmaceutical industry.

REFERENCES

  1. India Biodiversity Portal (2016) Online Portal of India Biodiversity.
  2. USDA-ARS (2015) Germplasm Resources Information Network (GRIN). Online Database. Beltsville, Maryland, USA: National Germplasm Resources Laboratory.
  3. PROTA (2015) PROTA4U web database. Grubben GJH, Denton OA, eds. Wageningen, Netherlands: Plant Resources of Tropical Africa.
  4. Acevedo-Rodríguez P, Strong MT (2012) Catalogue of the Seed Plants of the West Indies. Smithsonian Contributions to Botany. Washington DC, USA: Smithsonian Institution. pp: 98-1192.
  5. Flora of China Editorial Committee (2015) Flora of China. St. Louis, Missouri and Cambridge, Massachusetts, USA: Missouri Botanical Garden and Harvard University Herbaria.
  6. Talele BD, Mahajan RT, Chopda MZ, Nemade NV (2012) Nephroprotective plants: A review. Int J Pharm Pharm Sci 4(1): 8-16.
  7. Aneja KR, Joshi, Sharma C (2010) Potency of Barleria Prionitis L. bark extracts against oral diseases causing strains of bacteria and fungi of clinical origin. N Y Sci J 3: 5-12.
  8. Ata A, Naz S, Elias EM (2011) Naturally occurring enzyme inhibitors and their pharmaceutical applications. Pure Appl Chem 83(9): 1741-1749.
  9. Maji A, Bhadra S, Mahapatra S, Banerji P, Banerjee D (2011) Mast cell stabilization and membrane protection activity of Barleria prionitis L. Pharmacogn J 3(24): 67-71.
  10. Rahmatullah M, Azam MNK, Rahman MM, Seraj S, Mahal M, et al. (2011) A survey of medicinal plants used by Garo and non-Garo traditional medicinal practitioners in two villages of Tangail district, Bangladesh. Am Eurasian J Sustain Agric 5: 350-357.
  11. Sharma P, Shrivastava B, Sharma GN, Jadhav HR (2013) Phytochemical and ethnomedicinal values of Barleria prionitis L: An overview. J Harmo Res Pharm 2(3): 190-199.
  12. Sankaranarayanan S, Bama P, Ramachandran J, Kalaichelvan P, Deccaraman M, et al. (2010) Ethnobotanical study of medicinal plantsused by traditional users in Villupuramdistrict of Tamil Nadu, India. J Med Plant Res 4(12): 1089-1101.
  13. Katewa S, Galav P (2005) Traditional herbal medicines from Shekhawati region of Rajasthan. Indian J Tradit Knowl 4(3): 237-245.
  14. Mohammed S, Kasera PK, Shukla JK (2004) Unexploited plants of potential medicinal value from the Indian Thar desert. Nat Prod Radiance 3(2):69-74.
  15. Musale SB, Jagtap VA, Patil MS, Chittam KP, Wagh RD (2011) Diuretic activity of Barleria prionitis Linn flower extract. Int J Drug Discov Herb Res 1(1): 20-21.
  16. Reddy K, Trimurthulu G, Reddy CS (2010) Medicinal plants used by ethnic people of Medak district, Andhra Pradesh. Indian J Tradit Knowl 9(1): 184-190.
  17. Soni A, Krishnamurthy R (2013) Plants-the next generation treatment of leukemia. Indian J Plant Sci 2(1): 117-125.
  18. Khare CP (2008) Indian medicinal plants: An illustrated dictionary: Springer Science & Business Media.
  19. Ata A, Van Den Bosch SA, Harwanik DJ, Pidwinski GE (2007) Glutathione S-transferase and acetylcholinesterase-inhibiting natural products from medicinally important plants. Pure Appl Chem 79(12): 2269-2276.
  20. Bakshi SH, Lone SA, Rashid MT, Dar S, Shah KA (2012) Impact of calothrix sp. Apromotive biofertilizer on growth performance of Barleria prionitis in pot culture. Int J Life Sci Pharm Res 2(3): 287-292.
  21. Jaiswal SK, Dubey MK, Verma AK, Das S, Vijaykumar M, et al. (2010) Evaluation of iridoid glycoside from leave of Barleria prionitis as an antidiarrheal activity: An ethnopharmacological study. Int J Pharm Sci 2(3): 680-686.
  22. Kosmulalage KS, Zahid S, Udenigwe CC, Akhtar S, Ata A, et al. (2007) Glutathione S-transferase, acetylcholinesterase inhibitory and antibacterial activities of chemical constituents of Barleria prionitis. Z Naturforsch B 62(4): 580-586.
  23. Ata A, Kalhari KS, Samarasekera R (2009) Chemical constituents of Barleria prionitis and their enzyme inhibitory and free radical scavenging activities. Phytochem Lett 2(1): 37-40.
  24. Dheer R, Bhatnagar P (2010) A study of the antidiabetic activity of Barleria prionitis Linn. Indian J Pharmcol 42: 70-73.
  25. Chetan C, Suraj M, Maheshwari C, Rahul A (2011) Screening of antioxidant activity and phenolic content of whole plant of Barleria prionitis Linn. Int J Res Ayurveda Pharm 2(4): 1313-1319.
  26. Ganga Raju S, Naidu K, Chakradhar V, Prasad R (2002) Anthraquinones from Barleria prionitis. Indian Drugs 39(7): 400-401.
  27. Harborne J, Subramanian SS, Nair A (1971) Scutellarein 7-rhamnosylglucoside from Barleria prionitis. Phytochemistry 10(11): 2822-2823.
  28. Jeyasankar A, Premalatha S, Krishnappa K, Elumalai K (2013) Larvicidal activity of Barleria prionitis L (Acanthaceae) against japanese encephalitis vector, Culex tritaeniorhynchus Giles (Diptera: Culicidae). Int J Interdiscip Res Rev 1(2): 116-120.
  29. Chen JL, Blanc P, Stoddart CA, Bogan M, Rozhon EJ, et al. (1998) New iridoids from the medicinal plant Barleria prionitis with potent activity against respiratory syncytial virus. J Nat Prod 61(10): 1295-1297.
  30. Manjusha, Kumar V, Singh S (2013) Gastroprotective activity of methanol leaves extract of Barleria prionitis Linn. on Ethanol and Indomethacin Induced Ulcer in Rats. J Pharm Res Int 3(4): 817-829.
  31. Singh B, Chandan BK, Prabhakar A, Taneja SC, Singh J, et al. (2005) Chemistry and hepatoprotective activity of an active fraction from Barleria prionitis Linn in experimental animal. Phytother Res 19: 391-404.
  32. Choudhary M, Kumar V, Gupta PK, Singh S (2014) Anti-arthritic activity of Barleria prionitis Linn. Leaves in acute and chronic models in Sprague Dawley rats. Bull Fac Pharm Cairo Univ 52(2): 199-209.
  33. Kapoor A, Shukla S, Kaur R, Kumar R, Lehra KS, et al. (2014) Preliminary Phytochemical Screening and antioxidant activity of Whole plant of Barleria prionitis linn. Int J Adv Pharm Biol Chem 3(2): 410-419.
  34. Amit K, Shiwani S, Rajesh K, Rajinder K, Singh LK, et al. (2014) Pharmacognostical, Preliminary Phytochemical Screening and Antimicrobial Studies of Leaves of Barleria prionitis Linn. Int J Pharmacogn Phytochem Res 6(2): 369-378.
  35. Dheer R, Bhatnagar P (2010) A study of the antidiabetic activity of Barleria prionitis Linn. Indian J Pharmcol 42: 70-73.

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