Uterotonic

Oxytocin is a peptide hormone produced in the hypothalamus that plays an important role in many physiological functions. These functions include, enhancing mood and social relationships, promotion of maternal behaviors and stimulations of uterine contractions, among others roles. Uterine muscle contractions are induced via a G-protein pathway stemming from the oxytocin receptor (OXTR), the binding and activation site of oxytocin.[7] When oxytocin binds to its associated receptors in the uterus, a cascade is initiated that results in an increase in calcium and subsequently an increase in muscle contractions. The release of oxytocin helps to facilitate stronger contractions during labor to aid in delivery of the fetus. Additionally, during pregnancy, the uterine muscles have an increased concentration of oxytocin receptors, leading to an increased response to oxytocin as well.[8]

Oxytocin is the most commonly used agent for labor induction. It is given intravenously since it is easily degraded by the body if given orally. While giving oxytocin, it is important to monitor the mother and the fetus, specifically the mother's uterine activity and the fetal heart rate. The more common side effects of oxytocin include tachysystole, hyponatremia, and hypotension. Tachysystole is an increased rate of uterine contractions. If this occurs, it can be managed by lowering the dosage of oxytocin. Hyponatremia is a decreased concentration of sodium in the body as a result of increased fluids. This occurs due to oxytocin's similar structure to vasopressin (antidiuretic hormone), which acts to retain water in the body. Hypotension, or low blood pressure, is also a common side effect due to oxytocin's ability to relax smooth muscle of vessels. In comparison to women in spontaneous labor, women in induced labor on oxytocin experience a longer latent phase, however the duration of labor after reaching active labor (when the cervix has reached 6 cm), the duration of labor is considered equal.[9]

The most common cause of postpartum hemorrhage is a loss of muscle tone in the uterus. Normally, the uterus will contract to constrict blood vessels and decrease the flow of blood to prevent bleeding out. However, if there is a loss of muscle tone, see uterine atony, there is an increased risk of bleeding. Oxytocin is the first-line pharmacological step to help prevent PPH and treat PPH.[8]

Oxytocin plays an integral role in regulation of many of the body's biological processes- especially labor regulation. Since its structure was revealed in 1953, it has been the subject of intensive research.[10] Some of the analogs produced from extensive modification of its chemical structure residues have produced drugs and therapies that are utilized as uterotonics. Similar to oxytocin, analogues bind to oxytocin receptors found along the muscles of the uterus and act as an agonist. During pregnancy, the number of oxytocin receptors increase until reaching their peak near completion of the pregnancy. An important note is that not all analogs of oxytocin work as an receptor agonist or as a uterotonic. Some may oppose uterine contractility such as atosiban.[11]

Carbetocin: A long-acting synthetic analog with a half-life 4-10 times longer than natural oxytocin, it is used to control postpartum hemorrhaging or bleeding after giving birth. Heat-stable carbetocin does not require refrigeration unlike oxytocin; an notable advantage for use in low medical resource areas.[12] It is approved for use in 23 various countries around the world (not approved in United States).[11] In Canadian and German guidelines, carbetocin is recommended as a first-line therapy treatment for post-partum hemorrhaging with notable efficacy when used with cesarean section deliveries.[10] Carbetocin has been shown to be more effective than oxytocin in preventing postpartum hemorrhaging as well. Common side effects of carbetocin include vomiting, fever, and hypertension- similar side effect profile to that of oxytocin.[10] Both carbetocin and oxytocin are listed on the World Health Organization's Essential Medicines List.[10]

• Demoxytocin
• (Thiazolidine-4-carboxylic acid)-oxytocin

Prostaglandins are derived from the cell membrane phospholipids through a series of enzymatic reactions. Phospholipase A2 cleaves arachidonic acid from membrane phospholipids and is eventually converted to prostaglandins by cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2). Due to this mechanism, prostaglandins have a presence in many areas of the body and allow for diverse physiological and pathological functions. Primarily known for its role in mediating inflammation: pain, swelling, redness, and warmth, prostaglandin synthesis is a target for many drugs. Inhibition of COX-1 and COX-2 by aspirin and non-steroidal anti-inflammatory drugs prevents the inflammatory response and can also prevent homeostatic functions of the stomach and GI system that may lead to ulcers and bleeding.[13]

Prostaglandins (PG) have been attributed to partaking in the mechanisms of uterine activity during labor. The presence of prostaglandins and PG receptors increases throughout the pregnancy and increase expression of oxytocin receptors as well. Along with the increase in oxytocin receptors to facilitate labor, prostaglandins also increase the intracellular concentration of calcium.[6] Two PG subtypes, E and F, play fundamental roles in labor, PG E receptors, activated by PGE1 and PGE2 are more uteroselective and will stimulate contraction or relaxation depending on the subtype. PG F receptors will stimulate myometrial contraction, although the stimulus from PG F receptors are inferior to oxytocin. For this reason, injectable PGs are not used as first line treatment. Adverse effects of injectable PGs include hypotension and pulmonary edema.[14]

Misoprostol: an analogue of PGE1, this injectable PG is a popular choice for PPH prophylaxis and treatment. Misoprostol is easily administered, considered safe, and is low cost. The routes of administration include sublingual, oral, vaginal, and rectal with greatest efficacy from sublingual and vaginal administration. Vaginally administered misoprostol had improved outcomes of inducing labor within twenty four hours compared to oxytocin, but was associated with uterine hyperstimulation.[15] Misoprostol is an agonist of EP1 and EP3 receptors, and can cause a greater stimulation at lower concentrations. At higher concentrations, the medication can suppress contractions.[14]

Carboprost: an analogue of PGF 2α, this prostaglandin contains oxytocic properties that permit a longer duration of action than the naturally occurring prostaglandins. The injectable prostaglandin is administered via intramuscularly or intramyometrial, and is used in clinical practice. The drug is contraindicated in those with reactive airway diseases. Side effects of this medication include hypertension, hypotension, pulmonary hypertension, vomiting and diarrhea.[14][6]

• Alprostadil: commonly known as PGE1, is a naturally occurring prostaglandin and vasodilator. Alprostadil has not been added to the guidelines to treat PPH. The medication is not indicated for inducing labor, PPH, nor women, but for erectile dysfunction.[14]
• Dinoprostone: commonly known as PGE2, has the ability to stimulate both contractility and relaxation in the uterus during pregnancy. The area of action differs for each effect, contraction occurs in the upper uterine segment while relaxation occurs in the lower uterine segment.[14] Not as efficacious for inducing labor when compared to other prostaglandins.[16]
• Dinoprost: also known as PGF 2α, is a naturally occurring prostaglandin which causes contraction via PG F receptors. Dinoprost was discontinued in 2015.[14]

Ergot Alkaloids refer to a set of medications derived from the rye ergot fungus with mixed receptor activity that work to increase uterine muscle tone.[8] Unlike oxytocinergic uterotonics, ergot alkaloids work primarily through agonistic activity of serotonin receptors along the smooth muscles of the uterine wall.

Ergometrine, also known as ergonovine. Ergometrine is the first drug to be isolated from the rye ergot fungus. Ergometrine is often used alongside oxytocin to treat postpartum hemorrhaging and has been found to more effective than the standard of oxytocin treatment alone.[10] Ergometrine has a relatively quick onset of action following intravenous administration (one minute) with the duration of action averaging 45 minutes (rhythmic contracts will persist for up to 3 hours following administration).[8]

Methylergonovine, a synthetic analog of ergometrine that is primarily used to treat postpartum hemorrhaging due to uterine atony.[10] Similar to ergometrine, methylergonovine works through agonism of the serotonin receptors found on the smooth muscles of the uterine wall. It has partial agonist activity on α-adrenergic receptors as well as weak antagonistic activity on dopamine receptors.[8] Methylergonovine is intravenously administered with onset and duration of action similar to that of ergometrine. Its most common side effect is hypertension. Methylergonovine is recommended as a second-line therapy in treating postpartum hemorrhaging due to uterine atony according to both the American College of Obstetricians and Gynecologists (ACOG) and the Royal College of Obstetrics and Gynecology. In 2012, ACOG published a warning regarding use of methylergonovine's usage in people with hypertension where it was suspected to have caused myocardial infarction and ischemia in those individuals.[8]