Atropine is a poisonous crystalline tropane alkaloid and is also used as anticholinergic medication. These are naturally found in Belladona (Atropa Belladonna) and in 1831 it was first extracted from this substance in a crystalline form. Since then many synthetic and non-synthetic substitutes of atropine have been developed and put into medical treatments despite the fact that it lacks therapeutic selectivity and adverse effects. Medically it is used to treat certain kinds of nerve agents and pesticide poisoning. It also manages the slow heart rates and is given to the patients during surgery in order to reduce saliva production. It is either directly pushed into the body through an intravenous route or is injected into the muscle. It is also available as an eye drop that dilates the pupil. This action of atropine starts within two minutes of application and the effect can last for upto an hour. It is basically used as an eye drop to treat uveitis and early amblyopia. The structure of atropine can be diagrammatically represented as follows.
[]
IUPAC name of atropine is benzene acetic acid, alpha-(hydroxymethyl)-8-methyl-azabicyclo {3.2.1} oct-3-yl ester endo-(±)-. The atropine structure shows that it is a tropane alkaloid. It is an enantiomeric mixture of d-hyoscyamine and l-hyoscyamine and most of its physiological effect is due to the presence of l-hyoscyamine. The atropine structure of the most commonly used atropine in medicine is given below.
[]
According to the above structure of atropine its chemical formula is designated as 1αH, 5αH – Tropane – 3 – α ol (±) – tropate (easter) and is commonly termed as atropine sulphate monohydrate. Chemically atropine is an antimuscarinic agent and most of its effects are generated as it binds itself with muscarinic acetylcholine receptors present in the body. In the human body, the level of CNS appears within 30 minutes to 1 hour of its intake and rapidly disappears with a half life within 2 hours from the bloodstream. About 60% of atropine is discharged with urine without any characteristic change and the rest 40% of it appears in the urine as conjugation and hydrolysis products. The major conjugation products are noratropine(24%), atropine-N-oxide (15%), tropic acid (3%) and tropine (2%).
Properties of Atropine
Atropines have some very distinctive properties that are significant to atropine action in the human body. Some of the physical and chemical properties are listed below.
Properties of Atropine |
Values |
Molecular mass |
289.4 g/mol |
Physical state |
White crystals or crystalline powder |
solubility |
1g in 90ml at 800C (water) 1g in 2.5ml at 600C (alcohol) 1g in 27 ml of glycerol 1g in 1ml of chloroform 1g in 25ml ether |
Melting point |
114 – 1160C |
pH |
It is alkaline in water |
PKa value |
9.8 |
Optical state |
It is optically inactive |
Stability in light |
Should be protected from light and kept in an airtight container |
reactivity |
Toxic fumes of nitrogen oxides are emitted upon decomposition by heating |
Sublimation point |
93- 1100C at high vacuum |
XlogP3 |
1.8 |
Hydrogen Bond donor count |
1 |
Hydrogen bond acceptor count |
4 |
Rotatable bond count |
5 |
Heavy atom count |
21 |
complexity |
353 |
Topological polar surface area |
49.8Å2 |
Covalently bond unit count |
1 |
Atropine Pharmacology
-
Atropin generally hinders the “rest and digest” activity carried out by the glands that are supported by parasympathetic nervous receptors. As atropine hinders acetylcholine which is the main neurotransmitter used by the parasympathetic nervous receptors thus, atropine becomes the competitive reversible antagonist of the muscarinic acetylcholine receptors.
-
In cardiac use, atropine behaves like a non-selective antagonist for muscarinic acetylcholinergic receptors. Thus, it increases the conduction of the atrioventricular nodes (NA) and rapids the firing of sinoatrial nodes (SN) of the heart and prevents the action of vagus nerves. This results in blockage of acetylcholine receptor sites and reduces bronchial secretion.
-
Atropine induced mydriasis in the eye that results in the contraction of the pupillary sphincter muscle which is normally stimulated by the secretion of acetylcholine. This in turn allows the iris to contract and dilate the pupil. Atropine helps in paralysing the ciliary muscle by inducing cycloplegia that allows proper refraction in children and relieves pain associated with iridocyclitis.
Uses of Atropine
There are many therapeutic uses of atropine in the medical field despite it being therupatively selective and have certain adverse effects. Therapeutic uses of atropine are mostly studied for the eyes, heart. It also plays an important role in inhibiting secretions from glands and as an antidote for organophosphate poisoning.
-
It is used as a mydriatic to dilate pupils and as cycloplegic to temporarily paralyze the accommodation reflex of the eye. Many studies show that atropine penalization is very effective as occlusion in improving visual accuracy.
-
Atropine is useful in the treatment of heart block of second degree and third degree with high AV escape nodal rhythm or purkinje. In order to treat symptomatic or unstable bradycardia, atropine is injected into the muscles.
-
Atropine inhibits the secretion of saliva from the salivary glands by acting as a protagonist of the parasympathetic nervous system. As it also has the same effect on the sympathetic nervous system, it inhibits the secretion of sweat.
-
As it can mimic the side effects of antidepressants and few other medications it is used as an active placebo in many drug trials.
< li aria-level="1" readability="0">
Atropine helps in treating organophosphate poisoning by organophosphate insecticides and nerve agents by blocking the action of acetylcholine at muscarinic receptors.
Side Effects of Atropine
There are many side effects of atropine that have been observed over the years. For instance, excess doses of atropine sulphate cause difficulty in swallowing, dilated pupils, dizziness, fatigue, restlessness and even hinders coordination. If there is an extension of its dosage it may cause dryness of the mouth, fever, constipation, tachycardia, local allergy such as dermatitis, swelling of eyelids, conjunctivitis and sometimes the atropin drugs can cause atropine intox such as phenothiazines, antihistamines and TCA’s. As atropine has the ability to cross the blood brain barrier and because of its hallucinogenic properties, it causes hallucination and excitation especially among elderly people.