Show all

A STUDY OF THE PHARMACOLOGICAL EFFECTS OF METHANOL EXTRACT OF RIPE AND UNRIPE PLANTAIN (Musal Paradisiaca) ON ISOLATED GUINEA ILEUM

ATTENTION:

BEFORE YOU READ THE CHAPTER ONE/ABSTRACT OF THE PROJECT TOPIC BELOW, PLEASE READ THE INFORMATION BELOW.THANK YOU!

 

INFORMATION:

YOU CAN GET THE COMPLETE PROJECT OF THE TOPIC BELOW. THE FULL PROJECT COSTS N10,000 ONLY.

THE FULL INFORMATION ON HOW TO PAY AND GET THE COMPLETE PROJECT IS AT THE BOTTOM OF THIS PAGE. OR YOU CAN CALL: 08137701720

 

 

 

 

A STUDY OF THE PHARMACOLOGICAL EFFECTS OF METHANOL EXTRACT OF RIPE AND UNRIPE PLANTAIN (Musal Paradisiaca) ON ISOLATED GUINEA ILEUM

 

TABLE OF CONTENT

Declaration

Dedication

Acknowledgement

Abstract

Chapter one

Introduction & literature review

Chapter two

Materials and method

Chapter three

Results

Chapter four

Discussion

Chapter five

Conclusion

Tables and figures

References

 

 

 

 

 

 

 

 

 

 

 

 

ABSTRACT

For a large proportion of people in the delta regions of West Africa, Musa paradisiaca (plantain) is a staple food. Certain medicinal values have also been attacked to Musa paradisiaca, such as the use of unripe plantain in the treatment of diarrhoea. The aim of this project is to compare the pharmacological effects of methanol extracts of both ripe and unripe Musa paradisiaca, (plantain) of the motility of the guin a-pig ileum. This is an attempt to obtain any scientific basis for the use of unripe plantain pulp in ameloriation of diarrhoeal condition. 0.2ml of methanol extract of ripe plantain was administered into 20ml physiological solution in the organ bath. It antagonised the spasmodic effect of 10—8 to 10-6m dose range of acetylcholine. The acetylcholine dose-response curve was not surmountable. 0.5ml of the extract also antagonosed the dose-response curve for histamine non-competitively. Results show that the extract was not acting at the receptor site rather the effect of phyting, tarmin, or other substances present in the extract may have contributory effect in inhibition of contraction (Bagoosan, 1933; Goldstein, 1963; anon, 1945). Thin Layer chromatography (TLC) showed – bandy representing probably – possible compounds in the extract.

The methanol extract of unripe Musa paradisiaca produced contraction and a demonstrable dose-response relationship in the dose range of ten times to twop times dilution of the stock. The contractility elicited by the extract was antagonised by 0.5 x 10-6m atropine, in a non-competitive manner. 5 – hydroxytraptamine is the most abundant active physiological substance present in the plantain pulp which inhibits gastric acid secretion and stimulates smooth muslces of the interstine (Simmonds, 1966, 1966; smith et al; 1960). Calculations show about 10-6m of 6-hydroxytratamine in the extract. The spasmogenic activity may be the action of 5 –hydroxytryptamine. Thin Layer chromatography (TLC) showed – bands representing probably – possible compounds in the extract.

Pretreatment of the extract with chloroporm, and either conferred a spasmolytic activity to the unripe extract (Dede, 1986), (Affiong, 1988). This points to be fact that there are both spamogenic and spasmolytic ingredients in unripe Musa paradisiaca, while the ripe type contains only spasmolytic agents.

 

CHAPTER ONE

INTRODUCTION & LITERATURE REVIEW

  • BOTANICAL PROFILE OF Musa paradisaca

Plantain (Musa paradisiaca) and banana (Musa Sapienium), constitute a distinctive group in the order, called Zingiberales. According to the Hutchison’s classification, the order consists of six families of which Musacease is one.

Musaceae consists of two genera-ensete and musa. Musa consists of about 1, 400 species of which Musa paradisiaca is inclusive. Musa paradisiaca and other memebers of the Musa germs are tropical and subtropical perennial plants (Hutchison, 1959), (Simmonds, 1962).

Banana and plantain are derived from a hybrid of Musa acuminate and Musa balbisiana (Simmonds, 1962). There are no biochemical differences between plantain and banana rather, the differences are physical (William et al; 1972). Oyenyga; 1978, refers to plantain as a variety of banana which he termed Musa Sapientum var paradisiaca.

  • GEOGRAPHICAL & CLEMATIC DISTRIBUTION

Musa paradisiaca is favourably grown in humid lowland and is mostly grown between latitude 300 north and South of the equator. It has its origin from tropical Asia but it is now widely cultivated in other parts of the world such as West African countries, especially Cameron; India, Philippine’s; and Canary Islands. Wide distribution of Musa paradisiaca was brought about by man through explration (Smimmonds, 1962). Plantain has been given different names by different peoples. In Nigeria, the Ibos call it ogede, the Efiks call it Ukom. It is called Okinima by the Ikweres, Ode by the Urhobos and Dodo by the Yorubas.

  • PLANT MORPHOLOGY

The mature unripe plantain consists of a thick greenish skin and hardly pulp which is curved and elongated. It takes about 2-3 days for a fully mature and harvested green plantain to ripen into a soft Yellow fruit, if kept under the open air. During ripening period, there occur biochemical and chemical changes both in the pulp and the skin of plantain. (Simmonds, 1968). These changes include gradual loss of chlorophyll pigment and retention of caro tene matte leading to the yellowish appearance seen when ripe (Wardlaw, 1972).

There are also changes in sugar, starch and organic acid content as the green plantain ripens. Pulp oil increases while there is no significant change in the ash matter (Wardlaw, 1972). The sweet taste at ripening is due to increase in simple sugar level in the pulp. The plantain flavour increase in formation of esters and loss of tanmin ‘’astringency’’ in the ripe pulp (Loeseche, 1980).

          Plantain has a smooth, green, roundish stem, of about twelve feet tall. The leaves are the single, large type, arranged like that of palm tree, spirally, large type, arranged like that of palm tree, spirally, but closely around the upper part of the stem. The fruits are arranged in rings around the strong peducle. There are about 8-12 fingers in a ring, and about five rings in a bunch the proximal rings being bigger than those at the ends, giving the bunch an umbrella shape. The root can be regarded as an underground stem, from where new shoots spring up.

Time of shooting is between 1-7 months in the tropical lowlands. But this may extend to 18 months at 1000 metres of subtropical. It requires an average annual rainfall of 200-250 monometer well distributed. It can also be grown in areas with fairly dry season such as Uganda (pewrseglove, 1979).

  • MATERIALS OBTAINED IN Musa paradisiaca CAN BE CLASSIFIED INTO A, NUTREINTS (B) PHARMACOLOGICALLY ACTIVE COMPONENTS.
  1. Nutrients

Musa paradisiaca contains reducing sugars, starch, fat, amino acids, vitamins, minerals, moisture and ash.

Percentage (%) Nutrient composition. IN Musa paradisiaca,

NUTRIENT UNIUTEYE ACID%
Reducing sugar

Starch

moisture

Fat

Ash

0.18

32.00

45.00

0.90

2.90

20.00

2.00

75.00

2.40

6.11

The amino acid content is not known due to difficulty in amino acid extraction and identification.

TABLE 1 (Sowuni, 1980).

 

 

 

Percentage (%) composition of carbohydrate in Musa paradisiaca.

carbohydrate %composition(unripe) %composition (ripe)
Sucrose

Glucose

Fructose

Total sugar

starch

0.60

0.40

0.80

1.80

84.16

2.80

6.20

10.10

20.30

66.30

TABLE 2 (SOWUMI, 1980)

A 100gm unripe plantain will supply about 391.8 calories of energy (Oke, 1972).

The different Vitamins of Musa paradisiaca are: Ascorbic acid, thiamine, riboflavin, Miacin. They are found in variable amounts (Oyemuga, 1978).

Vitamin content of Musa paradisiaca.

vitamins Concentration per 100g

of unripe plantain

Ascorbic acid

Thiamine

Riboflavin

Niacin

11.00mg

0.02mg

0.05mg

0.65mg

Table 3: (Oyenuga, 1978).

Musa paradisiaca is a rich source of calcium, phosphorus, iron and some other trace elements

  1. PHARMACOLOGICALLY ACTIVE COMPONENTS (UNRIPE)

The known pharmacologically active components of plantain, and the unripe type specifically can be classified into;

  • Phenolic amines
  • Tamin

Simmonds, (1968), reported the presence of phenolic substances in plantain. The most abundant was 3, 4 – dihydroxyethylamine (dopamine). Through dopamine is abundant in the skin of plantain, the level is insignificant in the pulp (Anderson et al, 1978). Other substances were later discovered, of which 5-Ht is the most abundant. Others include noradrenaline and tyramine.

AMINE COMPOSITION IN PARTS PER MILLION

PULP                       SKIN

Dopamine Trace 100
5 – HT 19-36 30-170
Noradrenaline 2 122
Tyramine 7 655

TABLE 4: (Smmonds, 1966).

Not much have been reported about changes in the levels these pharmacologically active substances at ripening, but 5 – HT seems fairly constant in the pulp of the fruit and increases in the skin when ripe (Simmonds, 1966).

Bucley (1966), gave the biosynthetic pathway for phenolic amine synthesis in plantain thus

BIOSYNTHETIC PATHWAY FOR PHENOLIC AMINE SYNTH ESIS IN PLANTAIN.

The pathway starts from tyrosine, which is converted to tyramine, then to dopamine, and finally to noradrenaline in plantain pulp or skin.

5-Hydroxytryptamine (5-HT) is the most abundant pharmacologically active substance present in the plantain pulp. It inhibits gastric acid secretion and stimulates smooth muscles of the intestine (Simmonds, 1966; smith et al; 1960). Simmonds, 1966, reported the usefulness of this in combating coeliac disease.

The synthetic pathway for 5-HT has not been fully elucidated, however, it is presumed to be similar to the pathway in many other animals. Tryptophan is the precursor, and it is excreted as 5-hydroxy-indoleacetic acid in mammals, after eating plantain (Simmonds, 1966).

(II)     TANNIN

Tannin occurs in unripe plantain (Goldstein, 1963).

Tannin is responsible for the astringent property of plantain. Astringency has been defined as the formation of tannin-protein complex in the mouth and intestine. Astringent activity leads to various buccal, gastric and intestinal secretion arrest by tannin acid-containing vegetable products (Butherworths, 1978).

In unripe plantain the bulk of tanniins is Leucoanthocyanidin which is present as a monomeric falvo – 3, 4- diol or as oligomers and is believed to condense to inactive high tannin polymers at ripening. Polymerization leads to decreased solubility of high molecule tannins in methandic solvents (Goldstein et al; 1963).

Probable site of polymerization to give an inactive condensed tannin as seen in ripe plantain (Simmonds, 1966).

Othe4r phenolic substances present in banana include histidine, Leucodelphinidin, Eugenol, elemicin

Baggosan (1932), reported the presence of phytin in plantain. Phytin is a calcium-magnesium salt of phytic acid has been shown to interfere with the absorption of calcium either by precipitation or by converting it to a form which is not readily absorbed from the intestine. (Anon, 1945). Inositol is a basic sugar alcohol called myoinositol and is present in the form of phosphatidly inositol (Phytic acid) in the extracellular compartment of higher plant tissues (Lehninger, 19677).

Phytic acid has been shown to produce a negative calcium balance by binding as non-ionizable complex thereby reducing absorption considerably (Anon, 1945).

  • ECONOMIC/MEDICINAL USES OF Musa paradisiaca

Musa paradisiaca have been associated with antispasmodic action and implicated in antidarrhoeal management. There are other myriad of pharmacological actions associated with plantain, hence its use in diverse conditions, in addition to being a source of food for man.

The medicinal uses of Musa paradisiaca. Vary from locality to locality. This is presented in a tabular from below.

 

 

 

 

 

PART OF PLANT MEDICINAL USES.    
Sap-given above or with food For management of diarrhoea (Dalziel, 1936).  
 

 

pulp

For control of diarrhoea and related diseases in adult and children (Bethea; 1938).
pulp Normalizer of colonic functioning (Bogert; 1942)  
Pulp Relief of acute symptoms and to promote healing of intestinal lesion in chronic and acute ulcerative colitis (Voegtlin; 1936), Lestein, 1939) (Bethea, 1938).  
Young leaves softened by slight heating For dressing wounds in Ghana.  
Ash of burned stem, leaf or fruit Dusting powder for ulcera (Dalziel, 1938).  
Sap of inflorescence For earache in Gambia.  
Petides For Stopping Bleeding From Cut In Senegal  
Young terminal leaves moisture with palm oil For dressing of burns in Uganda.  
 

Bracts and sterile flowers cooked with melon seed

Provide remedy for chapped lips (Dalziel, 1938).  
The core of stem after warming at fire Wrapped round the feet of children to soften the skin for extraction of Jiggers (Dalziel; 1938).  
Sap of stem For nervous condition like hysteria and epilepsy (Oliver; 1960).  
Plantain combined with other plants For treatment of diabetes (Oliver; 1960).  
Plantain drinks For management of high blood pressure (Kokwaro; 1979).  

         

The tradition applications and formulations have been severely criticised for lack of: standardization of its dosage regimen and specification of quantities related to the age or body weight. In spite of these setbacks, it has continued not only to provide modern medicine with a numbers of compounds, either useful in themselves or capable of improvement by chemical modification, but also has continued to meet the health care needs of the people, especially, in the developing countries.

Musa paradisiaca also makes a delicious meal. It is consumed in large quantity in the coastal regions of West Africa (William et al; 1980). Generally, the demand for plantain in Nigeria is relative low. However, it is one of the commonest food in the Niger Delta region (Oyenuga, 1968).

The pulp has high caborific value due to the high carbohydrate content. The pulp contains mainly simple sugars-fructose and glucose (Jay; 1970; Coursey; 1967).

The fruit is prepared by roasting; boiling; frying in oils; mashed into paste as fufu; or smoked for storage till when needed for use. The plantain skin when dried under the sun is a good materials to provide ash, rich in potash for soap making (Dalziel; 1936). The use of plantain for beer brewing has also recently been reported in some parts of Tanzania and Uganda.

The sap of plantain produces indelible stain in fabrics and can be stalk of the plant is pounded and smeared on the floor of native mud houses. Plantain also provides a good fibre for making ropes and brushes, from the peduncles.

  • RELEVANT PHYSIOLOGICAL & PHARMACOLOGICAL PROCESSES AND CONCEPTS.

The ileum like other parts of the small intestine consists of four histological layers. These are from outside, the serosa layer, the muscular layer, the submucosa, and the mucosa layer.

The serosa layer is a continuation of the mesentery and is tightly bound to the underlying muscle layer. The muscular layer consists of outer longitudinal layer and an inner circular layer. The tow muscular layers are separated at some points by the dysenteric nerve plexus. Stimulation of this plexus causes contraction of the muscular layers producing peristaltic wave along the entire gastrointestinal tract. The subnucosa consists of areolar tissue with blood and lymph vessels and the meissner’s nerve plexus. The mucosa consists of finger-like folds or villi which are modified for digestion and absorption of food substances.

 COURTESY, VAN DAN BROUCHE & LEMLI, 1980)

The smooth muscle layer of ileum is innervated by post-ganglionic fibre located in the plexus which is derived from both the sympathetic and parasympathetic divisions of the post-ganglionic parasympathetic fibres with the liberation of cholinergic nero transmitter acetylcholine leads to increase in the motility and tone of the gut while stimulation of the sympathetic fibres causes moradrenaline release which causes a decrease in the tone and motility of the ileum.

An indept review of the gastro-intestinal physiological provides an insight into the general principles of intestinal motility which will help in laying a good foundation for a better understanding of interstinal motility both vivo and invitro. It will also help to appreciate the effects of drugs on the gastro-intestinal tract. Hence, sometime will be devoted to this topic.

The smooth muscle contains both actin and Myosin, the contractile proteins. Smooth muscle also contains tropomyosin but is is doubtful whether troponin or a tropomyosin-like substance exists in smooth muscle (Guyton, 1981). On stimulation of the muscle, there is an interaction between actin and Myosin, similar to that found in skeletal muscle. Furthermore, the contractile process is activated by calcium ions, and adenosine triphosphate (ATP) is reduced to adenosine diphosphate (ATP) to provide energy for the contrition.

The actual contractile process in skeletal and smooth muscles is activated by calcium ions. However, the source of calcium ions differ in smooth muscle bacuse the sarcoplasmic reticulum of skeletal muscle which is extensive and is the source of very nearly 100% of the contraction- inducing calcium ions. Due to the poor development of darcoplasmic reticulum in smooth muscle, most of the calcium ions used in contraction are obtained from extracellular fluid at the time of depolarization (Guyton, 1981). The lack of extracellular calcium or the intracellular blockade of calcium due to one factor or the other in smooth muscle results in muscle relaxation. Lack of calcium ion leaves the actin-nyosin fibres, cannot contractive state. The smooth muscle therefore, cannot contract (Hurwitz et al; 1972).

The gastro-intestinal tract is innervated by intrinsic and extrinsic nerves. The intrinsic innervation is the mycenteric and meissners plexuses. The extrinsic is the parasympathetic and sympathetic nervous supplies. The parasympathetic and sympathetic nervous supplies. The para-sympathetic nerves are stimulatory while the sympathetic nerves are inhibitory to the gastro-intestinal smooth muscles and

Glands.

The autonomic control of gastro-intestinal functions is not only exerted through adrenergic or cholinergic nerve fibres but also through inhibitory purinergic nerves with unknown postoganglionic neuro transmitters (Martinson, 1960). From the above discussion, it is possible that motility of the ileum can be modified by stimulating either the parasympathetic or sympathetic systems.

SPASMOGENS AND SPASMOLYTICS

Spasmogens are substances that can increase the contractility of smooth muscles. They are agonists. The spasmogens can act either at the receptor sites on the muscle membrane or on the nervous supply. Specialized and different receptor sites on the cell surface appear to be involved in response to each mediator. The selectivity of each of these types or receptors for certain types of chemical structures and the competitive kinetics between the structurally related substances which are often found, suggest that the ability to interact with each of receptor site is determined by its chemical structure (Daniel, 1964), fig 1.8 summarizes the sites of some drug effects in the guinea-pig ileum.

This discussion is useful in that by relating the different spasmogens with different action mechanisms, information on the pharmacological mechanism of action plantain extract can be revealed, especially when the effects of the extracts are related to the effects of the spasmogens.

Acetylocholine the acts directly on the smooth muscle by activating the cholinergic receptors. This activation is linked to CGMP. The acetylcholine-receptor interaction has been associated with increases release and depressed uptake of 42k+ in the muscle cells. (A.K Banergic and J.J Lewis, 1964). There is also evidence for a slight indirect action of acetylcholine, perhaps, through stimulation of ganglion cells (Feldbergy, 1951).

Histamine acts directly on the smooth muscle cells of the guinea-pig ileum (Kosterlitz & Robinson, 1958). Banerjee and J.J Lewis (1964), also reported increase in 42k+ release and depressed influx, associated with action of histamine. In the guinea-pig ileum (Gaddum & Pi carelli, 1957): the M receptors which are blocked by morphine and the D receptors which are blocked by phenoxybenzamine. The M receptors are generally assumed to be in nervous tissue and this is assumed to polay the major role in guinea-pig ileum contractility, while on the other hand, D receptors are found on the smooth muscles. 5 – HT also increase release and depresses uptake of 42k+ in smooth muscles. It has been suggested that 5-HT and 1, 1-dimethylphenyl-piperazinim activate different nerve-pathways; the acetylcholine released by 5-HT being hydrolysed mostly by acetylkcholinesterase whereas that released by dimethyphenyliperazinium, and also exogenous acetycholine is hydrolysed by a mixture of both butyryl and acetylcholinesterases (E.S. Johnson, 1964).

Nicotine; 1, 1-dimethylphenyl piperazinium, tetramethylammonium are all indirect spasmogens (Day and Vane, 1964). Other agents which are known to cause contraction of the gastro-intestinal tract include Ca2+, Ba2+ and Kcl.

SPASONDYTIC AGENTS

Atropine and related compounds, hyoscine and homatropine have been recommended and employed in a wide variety of conditions known or supposed to involve increased tone ‘’spasticity’’ or motility of the gastro-intestinal tract. Their antagonism of the muscarinic actions of acetylcholine is the basis of most, but not all, of their pharmacological actions. The ant muscarinic effect is associated with depressed release of 42k+ due to acetycholine (Banerjee & Lewis, 1964).

Other spasmolytic agents do so through interference with the role of calcium in excitation contraction coupling, like papaverine.

Inhibitors of oxidative phosphorylation also produce spasmolytic action, like papaverine (Ferrari, 1963).

The phosphodiesterase inhibitors like xanthines also make another group of spasmolytic agents.

  • DIARRHOEA AND DIARHOCAL THERAPEUTIC STRATEGIES

One of the most important clinical uses of antispasmodic agents is in the treatment of diarrhoea. Therefore, this introduction might not be complete if a brief discussion on diarrhoea is not made.

Diarrhoea is an increased loss of water and electrolytes, and is characterized by a stool weight greater than 200g per day. Diarrhoea may occur alone or in associated with increased fecal loss of other nutrients such as fat (Steatorrhea) or nitrogen (azo torrhea).

The increased fecal loss occur when the absorptive load exceeds the absorptive capacity. This can be caused by;

  • Increased absorptive load: This occurs in
  • High intake of food, like in excessive amount of tubne feeding. The high quantity of food may then start playing a kind of osmotic cathartic role
  • Decreased absorption: This is caused by intramural digestive disturbances, involving the mucosa or enzymes.

In the light of the above discussion, different approaches have been adopted for the treatment of diarrhoea. It is worthy of note that drugs prescribed for diarrhoea are determined on the cause or causation. Diarrhoea, therefore, may result from the following:

  • Eating of contaminated or partially decomposed food.
  • Bacterial or protozool infection.
  • Due to nervous disorder in GIT.
  • Due to inflammation of the intestine or. Adjacent viscera.

Diarrhoea may at times produce very serious consequences, for example, dehydration; exhaustion; loss of electrolytes, vitamins and food materials, hence need arises for medical intervention by the following means.

  1. Demulcnets and protective e.g salts of bismuth.
  2. Adsorbents e.g… Activated charcoal, chalk mixtures.
  3. Astringents e.g. Tannin.
  4. Antiseptics e.g. Antibiotics.
  5. Antispasmodics eg. Atropine, opiates. The antispasmodics are contra-indicated in diarrhoea caused by infections, such as bacillary dysentery, where by diarrhoea is an adaptive mechanism to evaluate the irritated intestine of the infected contents.
  6. Oral rehydration solution of water, salt and sugar.
    • AIM OF THE PROJECT

The aim of this project is to compare the pharmacological effects methanol extracts of both ripe and unripe plantain (Musa paradisiaca), on the motility of the isolated guinea-pig ileum. This is an attempts to obtain any scientific basis for the use of unripe plantain pulp in ameloriation of diarrhoeal condition.

HOW TO GET THE FULL PROJECT WORK

 

PLEASE, print the following instructions and information if you will like to order/buy our complete written material(s).

 

HOW TO RECEIVE PROJECT MATERIAL(S)

After paying the appropriate amount (#10,000) into our bank Account below, send the following information to 08137701720

(1)    Your project topics

(2)     Email Address

(3)     Payment Name

(4)    Teller Number

We will send your material(s) after we receive bank alert

 

BANK ACCOUNTS

Account Name: AMUTAH DANIEL CHUKWUDI

Account Number: 0046579864

Bank: GTBank.

 

OR

Account Name: AMUTAH DANIEL CHUKWUDI

Account Number: 2023350498

Bank: UBA.

 

 

NOTE:

YOU CAN ALSO MAKE A TRANSFER PAYMENT

 

FOR MORE INFORMATION, CALL:

08137701720

 

AFFILIATE LINKS:

www.easyprojectmaterials.com

www.easyprojectmaterials.net.ng

www.easyprojectsmaterials.net.ng

www.easyprojectsmaterial.net.ng

www.easyprojectmaterial.net.ng