Plant close view
Alhagi maurorum / اﻟﻌﺎﻗﻮل
SYNONYMS

Alhagi maurorum medik

ARABIC NAME

Al-Agool, Shouk Aljemal, Hai, Agool, Shabram, Al lahlah, Shouk, Aljam

COMMON NAME

Camel thorn

LOCAL NAME

Al-Agool, Shouk Aljemal, Shwaika

FAMILY

Fabaceae

Plant Habitat

Plant Habitat

Plant Habitat

Plant Habitat

Herbarium Sample

Herbarium Sample

Ethnobotanical Characteristics

Description

A shrubby evergreen perennial herb, woody base, erect to ascending up to 60(-100) cm high, very much branched with rigid spiny twigs about 1 in. long. Leaves deciduous simple, small, present at base of each side twig, obovate to oblong, shortly petiolate, with rounded tip, up to 2 cm. Flowers solitary or in pairs in axils and along twigs, with deep red to purple papillionate petals. Fruit a cylindrical pod, 1-3 cm, fairly thick straight , dark brown with constrictions between seeds; seeds 3-8 kidney shaped, smooth and brown.

Habitat & Distribution

It is a plant of tropical and subtropical regions, found in Africa, Asia, US, Europe and Middle East. Common in disturbed Urban sites, abundant along riverbanks, canals, irrigation ditches and sometimes in cultivated field. Common along Arabian Gulf Coast; less frequent inland.

Part(s) Used

Aerial parts

Traditional and Medicinal Uses

The plant is well known in India, Iran and Arabia. In U.A.E the plant is used as a general tonic, anthelmintic and to treat constipation, jaundice, arthritis, roots are used as aphrodisiac and it is a good fodder for camels. In other countries the plant is known to be diuretic, blood purifier, with antimicrobial activity, used for dysentery, upper respiratory system problems, wounds, hemorrhoids & uterus problems. 

Pharmacognosy and Phytochemistry

Parts studied

Leaves & branches

Microscopical Description

Leaves:

Both upper and lower epidermises are covered by thick cuticle. Epidermal cells of both surfaces are polygonal, periclincal of various sizes and shapes with straight to slightly wavy cell walls. Stomata in both surfaces are oval and of the anomocytic type. Upper epidermis is underlined by a single layer of hypodermis. The mesophyll is differentiated almost exclusively into elongated compact palisade parenchyma indicating the xeromorphic feature of the plant. The vessels of the embedded vascular tissues are annularly and spirally thickened.

Branches:

Transverse section of a young branch is circular in outline and its epidermis is also covered by a thick cuticle. The epidermal parenchyma cells are comparatively larger than those of leaf and the scattered stomata are also larger. Cortex comprises few layers of parenchyma cells. Phloem consists of compact tissues of lignified sieve tubes with parenchyma and companion cells. Tissues are frequently tranversed by medullary rays. The xylem consists of a wide continuous ring of lignified tissues composed of vessels, tracheids, fibers, xylem parenchyma and medullary rays. Vessels are annularly and spirally thickened. Pith consists of oval and rounded thick-walled parenchyma cells (Kamil et al.2001)

 Upper epidermis

a) Upper epidermis

T S of leaf

b) T S of leaf

TS of a leaf petiole

c) T S of petiole

a) Surface view of the upper epidermis showing its polygonal cells and underlying three large oblong hypodermal cells; oval stomata are also shown.

b) TS of leaf showing a layer of small rectangular upper epidermal cells underlain by large oblong cells of the hypodermis followed by relatively smaller palisade cells.

c) TS of a leaf petiole showing the heavily lignified vascular tissues. (Magnifications x400 x 400 and x 100, respectively).

Organoleptic characteristics

Appearance:                  Powder
Colour:                          Yellowish green
Odour:                           Aromatic
Taste:                             Acrid 

Physicochemical constants

Loss in weight on drying at 105°C (%):           9.2-9.5

Solubilities(%)

Alcohol solubility:                                             14.00 – 15.00
Water solubility:                                               23.00 – 24.00
10% ethanolic extractive:                                34.00 – 35.50

Ash values (%)

Total ash:                                                    11.20 – 11.40
Water soluble ash:                                      6.4 – 6.6
Acid-insoluble:                                            Nil

Successive extractive (%)

Petroleum ether (60-80°):                          4.6 – 6.8
Chloroform:                                               1.00 – 1.10%
Absolute alcohol:                                       8.1 – 8.2
Distilled water:                                           26.8 – 27.00

pH values

pH of 1%:                                                 5.73
pH of 10%:                                               5.42

Chemical constituents

Alkaloids, flavonoids, glycosides, steroids, terpenoids, resins and tannins are found in different extracts. Quantitative analyses of important inorganic elements have been performed in ash. (Kamil, et.al 2000; 2001).

Pharmacological and Toxicological studies

Both the ethanolic and chloroform extracts produced CNS stimulation in mice. Slight tremors, straub tail, rapid respiration, twitches, excitability and slight itching were recorded (Al-Yahya et. al., l985a). The extract caused an increased force of contraction of isolated rabbit heart and slight fall in blood pressure of anaesthetized rabbit (Al-Yahaha et. al., l985b) .The flavonoid fraction of the plant is reported to possess anti-inflammatory activity. The extract showed no significant effect on the level of serum glucose, cholesterol and potassium in rats. However, chloroform extract caused a decrease in serum sodium content. The extracts showed antimicrobial activity and are not toxic to Brine shrimps (Al-Yahaya et. al., l985 b).

The pharmacological and toxicological studies carried out in our laboratory and the results in brief, on Alhagi maurorum (10% ethanolic extract) have been given below. The results presented without references showed unpublished data (unpublished results, ZCHRTM, DBMS)

1. 10% Ethanolic Extract

ACTIVITY   RESULTS 
Anti-inflammatory activity-Rat paw oedema  Extract showed significant antiinflammatory activity in acute model (Zakaria et al., 1999).
Anti-inflammatory activity-Cotton pellet   Extract showed significant antiinflammatory activity in sub-acute model (Zakariaet al., 1999).
Antinociceptive activity-Tail flick  Extract showed antinociceptive activity.
Antinociceptive activity-Writhing  Extract showed antinociceptive activity.
Gastric ulcer activity- Indomethacin  Extract produced gastroprotective activity (Islam et. al., 200 a; Islam et. al., 200 b).
Gastric ulcer activity- Phenylbutazone  Extract produced gastroprotective activity (Islam et. al., 200 a; (Islam et. al., 200 b).
Gastric ulcer activity-NaOH  Extract produced cytoprotective activity (Islam et. al., 200 a; Islam et. al., 200 b).
 Gastric ulcer activity-Ethanol  Extract did not show cytoprotective activity (Islam et. al., 200 a; Islam et. al., 200 b).
 Sexual studies-Copulatory activity   Extract Extract showed significant sexual stimulant activity.
 Sexual studies-ICP  Extract increased intracavernous pressure.
 Testosterone quantification   Increased testosterone level in treated animals.
 Anti-hypertension activity- Anesthetic rats  Extract produced a transient increase in diastolic blood pressure, normalized after 30 min. Increased heart rate.
 Locomotor activity  Significant increase in locomotor activity was observed (Islam et al., 2000c).
 Gross behavioral studies-Tremor/Twitches   No toxic effect observed (Islam et al., 2000c).
 Gross behavioral studies-Writhing   No toxic effect observed (Islam et al., 2000c).
 Gross behavioral studies- Diarrhea, Urination  Produced no diarrhea and urination (Islam et al., 2000c).
 Mortality  No mortality recorded (Islam et al., 2000).
 Motor co-ordination (String and Platform test)  Motor coordination not affected (Islam et al., 2000c).
 Acute toxicity studies-  No toxic symptoms observed at the dose tested (Islam et al., 2000c).
 LD50 evaluation  > 10 g/kg (Islam et al., 2000c).
 Sub-acute toxicity studies  No significant symptomatic changes were observed (Islam et al., 2000c).
 Sub-chronic toxicity studies  Extract did not show any significant changes in body weight, vital organs studied (Islam et al., 2000c).
 Hematological studies  No changes in hematological parameters (Islam et al., 2000c).
 Biochemical studies  No changes in biochemical parameters except slight increase in plasma calcium and phosphorus (Islam et al., 2000c).
 Effect on body weight  No changes observed (Islam et al., 2000c).
 Effect on vital organ weight   No changes observed (Islam et al., 2000c).
 Teratogenicity  Extract did not show teratogenic effect; No foetotoxicity and maternal toxicity observed (Islam et al., 2000c).
 Mutagenicity  Extract did not show mutagenic (Clastogenic) activity as evidenced by micronuclei test (Islam et al., 2000c).

Summary of the results

Alhagi maurorum (10% ethanolic extract) showed significant antiinflammatory, analgesic, gastroprotective and sexual activity. The 10% ethanolic extract did not show serious toxic changes at the dose tested. No teratogenic and mutagenic effects were observed.

2. Aqueous Extract :

ACTIVITY   RESULTS
 Sexual studies-Copulatory activity  Extract showed sexual stimulant activity.
 Vasorelaxant activity-Isolated aortic strip  Extract produced relaxation in the contracted aortic strip.
 Cardiotonic activity & HR-Isolated rat atria Did not show any significant change. 
 Effect on GIT smooth Muscle-Isolated guinea pig ileum   Did not show any significant change in isolated Guinea pig ileum.
 Effect on GIT smooth Muscle-Isolated rat fundus   Produced contraction.
 Gross behavioral studies-Tremor/Twitches   No toxic symptoms observed.
 Gross behavioral studies-Writhing   No toxic symptoms observed.
 Gross behavioral studies-Diarrhea, Urination   No diarrhea and urination observed.
 Mortality   No death recorded.

Summary of the results

Alhagi maurorum (Aqueous ethanolic extract) showed significant sexual stimulant activity and showed no overt toxic signs and symptoms at the dose tested.

References

  • Al-Yahaya, M.A., Moussa, J.S., Al-Meshal, I.A. , Al-Badar, A.A., and Tariq, M., (l985a) Phytochemical and pharmacological studies for the treatment of fever, 4th South Asian /Western Pacific  regional Meeting of Pharmacologists. Penang, Malaysia.
  • Al-Yahaya, M.A., Moussa, J.S., Tariq, M., Al-Meshal, I.A. and Al-Badar, A.A. (l985b) Phytochemical and pharmacological studies on Saudi plants of family Leguminosae, 4th South Asian /Western Pacific Regional Meeting of Pharmacologists. Penang, Malaysia
  • Andrews, F.W. The Flowering Plants of Anglo-Egyptian Sudan; (1950&1952) vol 1+II; Arbroath, Scotland.
  • Department of Biomedical Sciences, Zyed Complex for Herbal Research and Traditional Medicine, Unpublished results.
  • El-Ghonemy, A. A. Encyclopedia of Medicinal Plants of the United Emirates. (1993)1st Edition, University of U.A.E.
  • Islam, M.W. Zakaria, M.N.M. Radhkrishnan, R.. Chan K ,and Al-Attas. A. Effect Of Alhagi maurorum Medilc. (Leguminoseae) on Acute Gastric Lesions in Rats. 1st International Congress on  Traditional Medicine & Materia Medica, Tehran 2000.
  • Jongbloed, M.V. The Comprehensive Guide to the Wild Flowers of the united Arab Emirates, Erwda, (2003) Emirates Printing Press, Dubai, U.A.E.
  • Kamil M, Ahmad F, Jairaj A F , Gunasekar C, Thomas S, Chen K & Attas A. Pharmacognostic and Phytochemical studies on aerial parts of Alhagi maurorum Medik . Hamdard Medicus ,2001 ,.XL1V ,No. 3: 57-71.
  • Kamil M, Ahmad F, Jairaj A F , Gunasekar C, Thomas S, Chen K & Attas A. Quality control Protocols for Alhagi maurorum 48th Annual Meeting of soc. For medicinal Plants Res. Natural Product Research in New Millenium, Sep,2000 , Zurich, Switzerland:4-A/13.
  • Kotb, T. F. Medicinal Plants in Libya .Arab Encyclopedia House. (1985) Tripoli-Libya.
  • Mandaville,J.P. Flora of Eastern Saudi Arabia. (1990) Kegan Paul International Ltd. England.
  • Western, A. R. The Flora of United Arab Emirates, an introduction. (1986) Publication of the U.A.E University.
  • Zakaria, M.N.M., M.W. Islam, R. Radhakrishnan, H.B. Chen, A. Ismail, K. Chan and M. Habibullah. Pharmacological evaluation of antiinflammatory activity of Alhagi maurorum. J Pharm Pharmacol. 1999, 51 (Suppl): 118.
  • محمد العودات، جورج لحام النباتات الطبیة واستعمالاتھا،( 1988 ) الجزء الأول- الطبعة الثانیة.الأھالي، سوریا
  • ھانئ عرموش الأعشاب في كتاب: الاستخدامات الطبیة- العلاجیة- التجمیلیة- التصنیعیة. ( 1999 ) دار النفائس، دمشق، سوریا

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