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This research investigated the phytochemical and anti-inflammatory properties of methanol extract of Crateva adansonii stem bark. Although several edible and non-edible plants parts are used in inflammatory treatment, many record has been found of the use of Crateva adansonii stem bark. For this research, fresh stem bark of Crateva adansonii were collected from Asata village in Enugu State. The cuttings were authenticated at the Bioresource development centre. They were then dried at room temperature for one month in an open lab space, grounded into powder and weighed on a beam balance as 460.6g. The powder was soaked for twentyfour to fourty-eight hours in methanol to get a methanol extract and then concentrated into paste at a set temperature range of 30-550C in a water bath. A population of twenty adult wistar Albino rats was used for antiinflammatory test. The rats were divided into five (5) groups of four (4) albino rats each. They were administered 3% tween-80 mixed with dichloromethane extract of Crateva adansonii and the control was administered with 0.5ml of 3% tween-80. Acute inflammation was induced an hour after test substances were administered by injecting egg albumin in the subplanter region of the right hind paw and edema assessed by mercury displacement for a period of 0-180 minutes. Anti-inflammatory effect was significant within 30 minutes of induced edema with inhibition occurring in three phases of 0-30, 30-60, 60-90. 90-120 to 180 minutes. Inhibition was highest at the third phase. Crateva adansonii barks showed antiinflammatory effect by inhibiting “prostaglandin” synthesis an inflammatory mediator
Title Page ———————————————————————i
Table of Contents———————————————————–vi
1.2 Crateva Adansonii as a Plant————————————-5
1.4 Scientific Classification———————————————6
1.5 Properties ————————————————————-7
1.6 Research Aim and Objectives————————————-8
1.7 Background of Study————————————————8
CHAPTER TWO-LITERATURE REVIEW
2.0 Definition of Inflammation—————————————10
2.1 Principle of Inflammation —————————————10
2.2 Types of Inflammation ——————————————-12
2.3 Categories of Inflammation Mediated by the Immune
2.4 Mediators of Inflammation—————————————22
2.5 Histamine and Serotonin——————————————29
2.6 The Coagulation Mechanism————————————-30
2.8 The Kinin – Forming System————————————–36
2.9 Inflammation and Diseases —————————————-40
2.10 Ways of Treating Inflammation———————————–40 2.11 Immune Selective Anti-inflammatory —————————42 2.12 The Use of Herbs in the Treatment of Inflammation———43 2.13 Anti-Inflammatory Drugs——————————————44 2.14 Phytochemicals——————————————————-46 2.15 Glycoside—————————————————————47 2.16 Flavonoids————————————————————–47 2.17 Tannins—————————————————————–49 2.18 Saponins—————————————————————49
3.1 MATERIALS ——————————————————–51 3.1.1 Equipment/Apparatus Used ————————————–51 3.1.2 Animal Used———————————————————-54 3.2.1 Methodology ———————————————————-55 3.2.2 Extraction————————————————————–56 3.2.3 Preparation of Reagents for Phytochemical ——————-56 3.2.3 Phytochemical Analysis of the Extract ————————–57 3.2.5 Test for Alkaloide—————————————————57 3.2.6 Test for Saponin——————————————————58
3.2.7 Test for Terpenoids————————————————–58 3.2.8 Test for Anthraquinones ——————————————-58 3.2.9 Test for Coumarins—————————————————59 3.2.10 Test for Phlobatannins———————————————-59 3.2.11 Test for Flavonoids————————————————–59 3.2.12 Test for Tannins——————————————————59 3.2.13 Test for Saponin——————————————————60 3.2.14 Test for Resins——————————————————–60 3.2.15 Test for Steroids and Terpenoids ——————————–61 3.2.16 Test for Glycoside—————————————————61 3.2.17 Preparation of Reagents for Anti-Inflammatory Test——–62 3.2.18 Test for Anti – Inflammation Activity ————————–62 3.2.19 Thin layer Chromatorgaphy (TLC)——————————65 3.2.20 How to Run A TLC Plate——————————————66
4.0 Extraction ————————————————————73 4.1 Photochemical analysis of Crateva Adansonii Bark Extract-74
5.1 Discussion —————————————————————–75 5.2 Conclusion—————————————————————–76 REFERENCES——————————————————-77 APPENDIX————————————————————80
Inflation is a Latin word (inflammare) which is translated means to set on
fire. It is a complex biological response of vascular tissue to harmful stimuli
such as pathogens, damaged cells irritant. Inflammation is the reaction of
vascularized tissue to local injury caused by certain stimuli like infections,
chemicals and biochemical agents, thermal or other physical trauma,
antigen-antibody interaction etc (Carol, 1994). Without inflammatory
response, wounds will not heal and minor infections would be over weening.
Though inflammation aims at limiting damage and restoring function, some
enzymes and toxic products within phagocytic cells are released to the
extend of damaging the tissue. The advent of anti-inflammatory agents has
made inflammation which as been a threat to human life due to its complex,
multicontent, to loose its power. These anti-inflammatory agents or drugs
help reduce, pain by inhibiting inflammation as opposed to opioids, which
affects the central nervous system. It also prevent repairs, prevent and stop
the consequences of inflammation by acting on the body responses without
directly antagonizing the causative agent (Stedman, 2000). These anti
inflammatory process involves the process of balancing pro-inflammatory
acute-phase reactants (Russell et al. 2000), altering biochemical pathway
forming prostaglandins by inhibiting cyclooxygenase enzyme from
catalyzing the reaction, as a result, suppress, compensate and correct the
mechanical and structural abnormalities by assistive device. (Masumoto et
The inflammatory reaction is phylogenetically and ontogenetically the oldest
defense mechanism. The cells of immune system are widely distributed
throughout the body, but if an infection or tissue damage occurs. It is
necessary to concentrate them and their products at the site of damage.
Three major events occurring during this response:
1. An increased blood supply to the damaged tissue . It is performed by
vasodilation. The inflamed tissue look like containing greater number
2. Increased capillary permeability caused by retraction of the
endothelial cells. This permits larger molecules than usual to escape
from the capillaries, and thus allows the soluble mediators of
immunity to reach the site of inflammation.
3. Leukocytes migrates out of the capillaries into the surrounding tissues.
In the earliest stages of inflammation, neutrophils are particularly
prevalent, but later monocytes and lymphocytes migrate towards the
site of infection (Ashcroft et al.1999).
For the possibility of surrounding tissue damage, inflammatory responses
must be well ordered and controlled. The body must be able to act quickly in
some situations, for example to reduce or stop the lost of blood, whereas
tissue repair can begin later. Therefore a wide variety of interconnected
cellular and humoral (soluble) mechanisms are activated when tissue
damage and infections occur. On the other hand, if injury is negligible, the
body must have mechanisms which are able to stop tissue damage when the
agent is removed. The development of inflammatory reactions is controlled
by cytokines, products of plasma enzymes (complement, the coagulation
clotting, kinin and fibrolytic pathways), by lipid mediators (prostaglandin
and leukotrienes) released from different cells/ and by vasoactive mediators
from the mast cells, basophils and platelets. These anti-inflammatory
reactions differ. Fast-acting mediators such as vasoactive amines and the
product of the kininsystem, modulate the immediate response. Later, newly
synthesized mediators such as leukotrienes are involved in the accumulation
and activation of other cells. However, in inflammatory reactions initiated
by the immune system, the ultimate control is exerted by the antigen itself in
the same ways it controls the immune response itself. For this reason, the
cellular accumulation at the site of chronic infection or auto-immune
reactions where antigen cannot ultimately be eradicated, is quiet different
from the sites were antigenic stimulus can be rapidly cleared.
The nervous system can also participate in the control of inflammation
especially axon reflexes, but inflammation may be realized in non-nervous
tissues as well.
Inflammation may become chronic in certain settings where the acute
process characterized by neutrophil infiltration and swelling gives way to
predominance of mononuclear phagocytes and lymphocytes.This probably
occurs to some degree with the normal healing process but becomes
exaggerated and chronic when there’s ineffective elimination of foreign
materials as in certain infections (e.g tuberculosis) or following introduction
of foreign bodies (example asbestos) or deposition of crystals (example urate
crystals). Chronic inflammation is often associated with fussion of
mononuclear cells to form multinucleated gigantic cells, which eventually
become granuloma. Chronic inflammation is seen under of delayed
hypersensitivity (Nathan, 2002).
1.2 CRATEVA ADANSONII AS A PLANT.
The flowering tree crateva religiosa (syn crateva adansonii) is called the
sacred garlic pear and temple plant, and many other names in a variety of
dialets, including Balai, lamok, abiyuch, barna, varuna and bidasi. The tree
is sometimes called the spider tree because the showy flower bear long,
spidery stamens. It is native to Japan, Australia, much of South East Asia
and several South east Asia and several South pacific islands. It is grown
elsewhere for fruit especially in part of African continent.
The crateva adansonii plant is a moderate sized, spreading unarmed,
deciduous tree growing to a height of 15 meters. Bark is grey, the wood
yellowish-white turning light brown when old. Leaves are clustered at the
end of the branchlets with a common petiole 5-10 centimeter long, at the
summit of which are three leaflets. Leaflets are ovate-lanceolate or ovate
7.5-12 centimeter long, 4-6 centimeter wide. Pointed at the base rather
slender pointer at the tip. Flower occur in terminal corymbs, about 5
centimeters in diameter, greenish yellow, and at length purplish.
Petals are ovate or oblong with the claw haft as long as the limb. Fruit is
ovoid or rounded, 3-5 centimeter in diameters, with a hard and rough rind.
Seeds are about 10 centimeter in length, numerous kidney-shaped, and
embedded in a yellow pulp.
1. In waste places, along streams and in thickets near the sea.
2. Occurs in India, Myanmar, Sri lanka, Malasia, Indonesia and
China. (nature serve. 2011).
3. Sometimes planted as ornamentals tree for its beautiful flower.
1.4 SCIENTIFIC CLASSIFICATION
Sub- class: Rosids
The constituents of the plant have been assessed overtime and it has been
found in various parts of the plants to contain:
Bark yield tannin.
Phytochiemicals screening of extract of dried leaves yielded allcaloids,
carbohydrates, tannin, flavonoids, resins, proteins, oils, steroids and
Generally considered diuretic, anti-inflammatory, laxative, anti-oxidant,
hepatoprotective, antilithics, antirheumatic, antiperiodic, contraceptive,
Bark has a disagreeable smell, the taste slightly bitter, bitting and pungent.
Leaves considered stomachic and tonic.
Roots and bark considered laxative, lithotriptic and alternative, promoting
appetite and increasing biliary sections.
Leaves are rubifacient, tonic and febrifugal.
1.6 RESEARCH AIM AND OBJECTIVES
This research aim at investigating the anti-inflammatory properties of
methanol extract of crateva adasonii stem bark. And as objectives, to
compare the therapeutic potential, (i.e. anti-inflammatory effect ) of the
methanol extract of crateva adansonii bark against the experimental
1.7 BACKGROUND OF STUDY
The plant crateva adansonii also known as or also called sacred garlic pear
and temple plant. Apart from its medicinal properties which allows the
plants to be used as laxative, it is also an edible plant especially the fruits,
berry and young shoot. The plant is used in herbal treatment of tympanites,
convulsion, treatment of fever, rheumatism, urinary calculi etc.
Crateva adansonii is capable of suppressing the free radicals, production, it
is been suggested to have anti-inflammatory properties which counter the
synthesis of inflammatory mediators thus forming the background of this