Download as pdf or txt
Download as pdf or txt
You are on page 1of 70

DRUGS ACTING ON GIT

Presented by
Dr. Sannithi Nagarjuna

Coordinator for RIPER-GPAT Cell,


Hyderabad Academy &
Online GPAT Academy
7899107907

9885784793

nagarjunaspharma@gmail.com
Diseases - Caused by pathogenic/harmful microorganisms

e.g. Tuberculosis, Leprosy, Typhoid, Malaria

Disorders - due to altered/abnormal functioning of any body


system

e.g. Diabetes mellitus, Peptic ulcer, Hypertension, Hypotension,

Hyperthyroidism, Hypothyroidism
PHYSIOLOGY → Study of normal functioning

of body systems

PATHOPHYSIOLOGY → Study of disorders

PHARMACOLOGY → Study of drugs


MAJOR PARTS OF GIT

1. Stomach → acid/Hcl secretion → digestion(decrease in size),


→ To kill Microorganisms

2. Small Intestine → Absorption

3. Large Intestine → Unabsorbed substances eliminated through

feces and the process called as defaecation


SMALL INTESTINE

LESS PARTICLE SIZE ( DIGESTED COMPOUNDS WILL REACH)

LARGE SURFACE AREA ( DUE TO VILLI AND MICROVILLI)

LIPOPHILICITY

NONPOLAR

UNIONIZED FORM ( WEAK ACIDIC TO WEAK BASIC PH AND MOST OF


PHARMACEUTICAL DRUGS ARE EITHER WEAK ACIDS OR WEAK
BASES)
DISORDERS RELATED TO GIT

1. Peptic Ulcer ( Increased secretion of acid )

2. Achlorhydria ( decreased/ absence of acid secretion)

3. Emesis

4. Diarrhoea ( Increased passage of stools)

5. Constipation (Decreased passage of stools)


DRUGS ACTING ON GIT

1. Antiulcer drugs

2. Drugs for Achlorhydria

3. Emetics & Antiemetics

4. Antidiarrhoeal agents

5. Dugs for constipation/Laxatives


PEPTIC ULCER
❖ Characterized by excessive secretion of acid (acidity)

❖ Ulcers mean injuries/wounds due to long term existence of acidity

❖ Occurs in the areas highly exposed to gastric acid

❖ Stomach and duodenum are highly exposed to acid

❖ Ulcers in the stomach called as gastric ulcers

❖ Ulcers in the duodenum called as duodenal ulcers


Source: Google
Homeostasis

Maintenance of balance /equilibrium inside the body called as


homeostasis.

The major reason for disorders is disturbance in homeostasis.

Ex:

Maintenance of acid secretion, body temperature, blood

pressure, pulse rate etc.


Homeostasis (Acid secretion)

Aggressive factors = Defensive factors


(which ↑ acid secretion) (which ↓ acid secretion)

e.g. e.g.
Acetylcholine Mucus

Histamine HCO3-
Gastrin PGs
ETIOLOGY/CAUSE
Disturbance in homeostasis

↑ Aggressive factors ǂ ↓ Defensive factors


e.g. e.g.
Acetylcholine Mucus

Histamine HCO3-
Gastrin PGs
Helicobacter Pylori
Source: Google
Source: Google
Source: Google
ANTIHISTAMINES(H2 RECEPTOR BLOCKERS

Cimetidine - first drug, antiandrogenic action, withdrawn


from the market

Ranitidine - Popular brand names are RANTAC,


ZANTAC

Famotidine - Most potent drug


Proton Pump Inhibitors (H+ k+ ATPase Inhibitors)

❑ Highly effective

❑ Long term use decrease the release of intrinsic factor


which is essential for the absorption of vitamin B12 that
results in pernicious anemia
ANTICHOLINERGICS

❖Nonselective drugs have side effects like dry


mouth, dry skin, dry eye

❖Selective M1 blockers are preferred


PG ANALOGUES
• Decrease acid secretion

• Increase bicarbonate and mucus secretion

• Also called as cytoprotective agents

• Used to treat NSAIDs induced ulcers


NSAIDs inhibit Cyclooxygenase and inhibit the production

of PGs that result in ulcers ( PGs are defensive factors).


GASTRIN ANTAGONISTS

Proglumide cholecystokinin antagonist, which blocks both

the CCKA and CCKB subtypes .

Not preferred due to toxicity


ANTACIDS

Antacids are basic/alkaline substances due to

their alkalinity they will neutralize the gastric acid.


SYSTEMIC ANTACIDS

They enter into systemic circulation, they produce

systemic alkalosis and they are not preferred due to

this reason.
NONSYSTEMIC ANTACIDS
They will not enter into systemic circulation, produce local action and

they are highly preferred.

Aluminium salts produce constipation and magnesium salts produce

laxation, hence both should be used in combination.

MAGALDRATE is a combination of both in the body broken down into

aluminium hydroxide and magnesium hydroxide.


Source: Google
ULCER PROTECTIVES

They form a layer on the ulcers and they will protect

the ulcers from direct exposure to acid or any other

irritants
ULCER HEALING DRUGS

Carbenoxolone sodium obtained from Glycyrrhiza glabra

( Liquorice).

Due to lignin content and saponins they exhibit wound healing

property.
ANTI H.PYLORI DRUGS

❖ H. Pylori is a gram negative bacteria

❖ Treatment includes some of antibacterials and


antiprotozoals
DRUGS FOR ACHLORHYDRIA

❖ Rarest condition

❖ Majorly seen in children till 3 years of age

❖ Due to this they have frequently indigestion, vomiting and

infections

❖ Drugs used include Cholinergics like Carbachol, Bethanechol


EMETICS & ANTIEMETICS

Emetics are the agents which produce nausea and vomiting.

The only use of emetics is in the treatment of poisoning.


But they have some limitations like/they are not suitable in the
following conditions:

❖ If the patient is unconscious

❖ If the poison is already absorbed

❖ If the poison is strong acid/ strong base/corrosive which cause


further damage to the oesophagus

❖ If the poison is detergents/petroleum products which could be


aspirated into lungs

❖ Substance ingested likely to cause rapid onset of drowsiness or


seizures
Examples:

❑ Apomorphine

❑ Ipecacuanha (Emetine)

❑ Mustard

❑ Salt water
ANTIEMETICS:

These are all agents which prevent or stop the

occurance of nausea and vomiting.


CONDITIONS ASSOCIATED WITH VOMITING

Motion sickness (Vomiting during Journey/motion)

Morning sickness ( Vomiting during pregnancy)

Drugs like Levodopa

Conditions like Migraine

Anticancer drugs and radiation therapy

Excessive eating, excessive drinking & Bad smell/odor


Vomiting occurs due to stimulation of Vomiting centre (Emetic centre).

Vomiting centre is controlled by two centres named as CTZ

(Chemoreceptor Trigger Zone, located in CNS) & NTS (Nucleus

Tractus Solitarius, located in GIT).

CTZ is having receptors like D2, 5-HT3 & NK1 receptors and stimulation

of CTZ takes place due to stimulation of any one of the receptors.

Stimulation of NTS takes place due to excessive stimuli from

stomach.
MOTION SICKNESS

Any form of travel on land, in the air or on the water can


bring on the uneasy feeling of vomiting.

Children between the ages of 2 and 12 are most likely to


suffer from motion sickness.

Motion sickness is caused by a conflict between signals


arriving in the brain from the inner ear, which forms the
base of the vestibular system, the sensory apparatus that
deals with movement and balance, and which
detects motion mechanically.

Motion sickness occurs due to stimulation of muscarinic


and H1 receptors in vestibular apparatus which further
stimulates CTZ.
Receptors Present in CTZ Reason for the Stimulation
D2 Morning sickness
(Vomiting during pregnancy)

Drugs like Levodopa

Conditions like Migraine

5-HT3 Anticancer drugs and radiation


therapy

NK1 Excessive release of substance


P due to chemotherapy

Stimulation of NTS takes place due to excessive stimuli from

stomach observed in case of excessive eating, excessive drinking &

bad smell/odor.
CLASSIFICATION OF ANTIEMETICS
1. Anticholinergics

2. Antihistamines (H1 receptor blockers)

3. D2 receptor blockers (Neuroleptics)

4. 5-HT3 receptor blockers

5. NK1 receptor blockers

6. Gastroprokinetic agents

7. Adjuvant antiemetics
ANTICHOLINERGICS

Ex: Hyoscine (Scopolamine),

Dicyclomine

Hyoscine available as transdermal patches and those

patches applied behind the pinna.


ANTIHISTAMINES (H1 RECEPTOR BLOCKERS)

Ex: Promethazine,

Diphenhydramine,

Dimenhydriate,

Cyclizine

Anticholinergics and antihistamines exclusively used for the

treatment of motion sickness and they should be taken atleast 1

hour before the commencement of journey and they are also

effective in morning sickness.


D2 RECEPTOR BLOCKERS
(NEUROLEPTICS)

Which are mainly used to treat

❖ Morning sickness (Vomiting during pregnancy)

❖ Levodopa induced vomiting

❖ Migraine induced vomiting

Ex: Chlorpromazine, Haloperidol- Extrapyramidal side


effects (Parkinsonism like symptoms)
5-HT3 RECEPTOR BLOCKERS

Which are mainly used to treat

❖ Anticancer drug induced vomiting

❖ Radiation therapy induced vomiting

Ex: Ondansetron, Granisetron


NK1 RECEPTOR BLOCKERS

Which are used to treat substance P induced

vomiting due to chemotherapy and in case of injuries

Ex: Aprepitant
GASTROPROKINETIC AGENTS

Which increase the motility of GIT allowing the fast passage of

contents from stomach to intestine.

As a result of this mechanism contents present in stomach for less

time hence there is no chance of vomiting.

Due to this mechanism they produce diarrhoea as a side effect.

They stimulate 5-HT4 receptors present in GIT allowing the release

of Acetylcholine which increase the peristaltic movement of GIT.


Ex:
Metoclopramide→ also has D2 receptor blockade mechanism

Domperidone → also has D2 receptor blockade mechanism

Cisapride

Mosapride

Tegaserod
ADJUVANT ANTIEMETICS

Which alone may not have antiemetic property but

they increase the activity of other antiemetics.

Ex: Benzodiazepines

Corticosteroids

Cannabinoids (DRONABINOL, NABILONE)


Condition Drug of Choice

1. Motion Sickness A) Metoclopramide

2. Levodopa induced vomiting B) Hyoscine

3. Chemotherapy induced vomiting C) Aprepitant

4. Substance P induced vomiting D) Cannabinoids

5. Gastroprokinetic with D2 receptor E) Haloperidol

blockade property

6. Adjuvant antiemetic F) Ondansetron


1. B

2. E

3. F

4. C

5. A

6. D
ANTIDIARRHOEAL
AGENTS
ANTIDIARRHOEAL AGENTS

❖ Used for the treatment of diarrhoea

❖ Diarrhoea is characterized by increase in the frequency of passage of


stools

❖ Mostly diarrhoea is a disease and very few cases it is considered as a


disorder.

❖ Most of the times diarrhoea occurs due to contamination with microorganisms


(Disease) and some times it occurs due to increased peristaltic movement of GIT
(Disorder).
❖ Appearance of more water in the stools called as watery/loose

stools → Indicates bacterial infection

❖ Appearance of blood in the stools called as Dysentery → caused by

Shigella

❖ Appearance of pus in the stools called as Amoebiasis → caused by

Entamoeba histolytica

❖ Severe vomiting with diarrhoea observed in case of Cholera →

caused by Vibrio cholera

❖ Fever with diarrhoea observed in case of Salmonella infection

❖ Travellers diarrhoea Caused by E.Coli


REHYDRATION
Severe diarrhoea results in dehydration, some times lead to death.
Severe stage of dehydration is identified by loss of urine output.

Dehydration will be corrected by Rehydration that can be done by


either oral route or IV depends upon the emergency.
Composition usually includes
Sodium chloride Electrolyte replacement

Potassium chloride Electrolyte replacement

Sodium Buffer
bicarbonate/Sodium
citrate
Glucose Nutrient replacement

Water Fluid replacement


Antidiarrhoeal agents are classified into two types:

I. Specific Antimicrobial agents


Which are used when the diarrhoea is caused by specific
microorganism

II. Nonspecific Antidiarrhoeal agents


Which are used when the diarrhoea is caused by
increased peristaltic movement of GIT
SPECIFIC ANTIMICROBIAL AGENTS

Antibacterials like
Ex:
Fluoroquinolones like Ciprofloxacin, Norfloxacin, Gatifloxacin,
Levofloxacin
Tetracyclines
Co-trimoxazole

Antiprotozoals like
Metronidazole, Tinidazole
NONSPECIFIC ANTIDIARRHOEAL AGENTS

They are classified into 2 types

I. ANTISECRETORY DRUGS ( Drugs which reduce PGs)

II. ANTIMOTILITY DRUGS


ANTISECRETORY DRUGS
( DRUGS WHICH REDUCE PGS)
1. SULFASALAZINE
Sulfasalazine

Azo Reductase

5-Amino Salicylic acid (5-ASA) + Sulfapyridine (Carrier)


(Active)

Inhibits COX in the colon

Inhibits PGs, Inhibits secretions & Motility


The official name given to 5-Amino Salicylic acid (5-ASA) is

MESALAMINE (MESALAZINE).

2. OLSALAZINE

Which consist of 2 molecules of 5-Amino Salicylic acid (5-ASA).

3. ANTICHOLINERGICS
ANTIMOTILITY DRUGS
Ex:

1. OPIOIDS
Morphine
Loperamide
Diphenoxylate

These drugs act through µ opioid receptors present on colon.

2. ANTICHOLINERGICS
DRUGS FOR CONSTIPATION
Constipation is characterized by decrease in the passage of stools

or difficulty in the passage of stools.

Drugs for constipation include

Aperients → Very milder


Laxatives → Milder
Purgatives → Stronger
Cathartics → very Stronger
CLASSIFICATION OF LAXATIVES
They are classified into 4 types

1. Irritant/Stimulant laxatives

2. Bulk forming laxatives

3. Osmotic/Saline laxatives

4. Surfactant laxatives/ Stool softeners


IRRITANT/STIMULANT LAXATIVES

❖ They act by increasing peristaltic movement of GIT

❖ They act by increasing PGs

❖ They act by increasing secretions


Ex:
1. DIPHENYLMETHANES : Bisacodyl

2. ANTHRAQUINONES : Senna, Cascara

3. FIXED OILS : Castor oil


BULK FORMING LAXATIVES

They are not digested and they are not

absorbed.

Due to indigestion, all bulky material reach to

the large intestine, increases bulkiness and

causes free passage of stools.


Ex:

Ispaghula (Isabgol)

Psyllium (Plantago)

Dietary fibres
OSMOTIC/SALINE LAXATIVES

They are not absorbed and they cause retention of

water.

Unabsorbed compounds will reach large intestine and

due to retention of water swelling takes place that

increases bulkiness.
Ex:

Magnesium Sulphate (Epsom Salt)

Magnesium Hydroxide (Milk of Magnesia)

Sodium Sulphate (Glaubers salt)

Sodium Potassium Tartarate (Rochelle salt)

Polyethylene glycol

Glycerine

Lactulose
Source: Google
SURFACTANT LAXATIVES/ STOOL SOFTENERS

Due to increased reabsorption of water hardening of


stools will result that causes difficulty in the passage of
stools.

Drugs are surfactants which reduce interfacial tension


and increases water incorporation that soften the
stools.

Ex: DOCUSATES (Dioctyl Sodium Sulfosuccinate),


MINERAL OIL
Presented by
Dr. Sannithi Nagarjuna

Coordinator for RIPER-GPAT Cell,


Hyderabad Academy &
Online GPAT Academy
7899107907

9885784793

nagarjunaspharma@gmail.com

You might also like