Summary: Neurosteroid replacement therapy may provide relief of symptoms for new mothers suffering from postpartum depression.

Source: Texas A&M

Postpartum depression affects about one in eight women, according to the Centers for Disease Control and Prevention. D. Samba Reddy a professor in the department of Neuroscience and Experimental Therapeutics in the Texas A&M University College of Medicine, is the lead researcher of a lab that may have discovered a treatment for postpartum depression, which has historically gone largely undiagnosed and unaddressed.

Over the last two decades, Reddy has conducted extensive research to develop a new treatment method that makes use of the body’s natural chemistry to treat brain diseases. He coined this term “neurosteroid replacement therapy” to reflect the methodology of other, more-familiar types of replacement therapies, such as insulin replacement therapy or hormone replacement therapy.

His most recent work applying this approach to postpartum depression is outlined in a paper recently published in the Journal of Neuroendocrinology.

Neurosteroids are steroids synthesized within the brain that have important regulatory effects on the brain’s function. One specific neurosteroid, allopregnanolone, is produced in increasing amounts during pregnancy. However, after childbirth, the neurosteroid levels drop, leading to chemical imbalances in the brain that can cause postpartum depression.

Enter what could be one of the most groundbreaking discoveries in women’s health: the formulation of allopregnanolone, in injection form, for treatment of postpartum depression. This medication, which was then renamed as brexanalone, was approved in 2019 as the first drug for postpartum depression.

How does the medication work?

Postpartum depression is unique in that there is a small window of time during which it can be treated; it varies from person to person, but the critical period is the first four weeks after the baby is born. The new mother’s body resumes the menstrual cycle after four to six weeks, and once the cycle starts, the body will start producing neurosteroids at normal levels again, and the new mother’s body is able to establish a rhythm.

“Before neurosteroid replacement therapy, there was no medicine available that worked quickly enough to treat postpartum depression,” Reddy said. “After childbirth, women don’t have weeks to wait on existing depression medications, which take at least three to four weeks before they take effect.”

One specific neurosteroid, allopregnanolone, is produced in increasing amounts during pregnancy. Image is in the public domain

Neurosteroids, on the other hand, work immediately as antidepressants because they have a rapid mechanism of action. They enhance an already-existing receptor in the brain, so when the drug is infused, the patient immediately starts feeling better, and after the recommended three-day duration of treatment, they’ll continue to feel better for weeks. This medication helps new mothers replace their neurosteroids for the first few weeks after birth until their bodies restart production of these neurosteroids naturally.

Why is postpartum depression a public health issue?

New mothers generally return home after a few days in the hospital, during which time they may or may not show the full symptoms of postpartum depression. As a result, and because new mothers are unlikely to report symptoms themselves, postpartum depression is a condition that needs to be identified by people observing the mother day-to-day. A partner, parent or friend may notice that the new mother is experiencing difficulties bonding with the baby, communicating her feelings or carrying out daily activities, and recognize that she needs help.

Therefore, it is vital that the public is made aware of both the symptoms of postpartum depression as well as the treatment that is available. In the past, postpartum depression wasn’t commonly acknowledged because there was no good solution.

“You don’t want to improve awareness about a problem when there’s no treatment,” Reddy said. “Telling someone that they have a disease but there is no treatment available can scare them.”

With the advent of this treatment, raising awareness of postpartum depression is an important component of how the public can address this pressing concern.

“With reassurance that there is a treatment available, I think women will feel more empowered to talk about postpartum depression and seek the help they need,” Reddy said.

About this postpartum depression research news

Author: Sunitha Konatham
Source: Texas A&M
Contact: Sunitha Konatham – Texas A&M
Image: The image is in the public domain

Original Research: Closed access.
“Neurosteroid replacement therapy for catamenial epilepsy, postpartum depression and neuroendocrine disorders in women” by Doodipala Samba Reddy. Journal of Neuroendocrinology


Abstract

See also

This shows a depressed looking man

Neurosteroid replacement therapy for catamenial epilepsy, postpartum depression and neuroendocrine disorders in women

Neurosteroids are involved in the pathophysiology of many neuroendocrine disorders in women. This review describes recent advancements in pharmacology of neurosteroids and emphasizes the benefits of neurosteroid replacement therapy for the management of neuroendocrine disorders such as catamenial epilepsy (CE), postpartum depression (PPD) and premenstrual brain conditions.

Neurosteroids are endogenous modulators of neuronal excitability. A variety of neurosteroids are present in the brain including allopregnanolone (AP), allotetrahydro-deoxycorticosterone and androstanediol. Neurosteroids interact with synaptic and extrasynaptic GABAA receptors in the brain. AP and related neurosteroids, which are positive allosteric modulators of GABAA receptors, are powerful anticonvulsants, anxiolytic, antistress and neuroprotectant agents. In CE, seizures are most often clustered around a specific menstrual period in women. Neurosteroid withdrawal-linked plasticity in extrasynaptic receptors has been shown to play a key role in catamenial seizures, anxiety and other mood disorders.

Based on our extensive research spanning two decades, we have proposed and championed neurosteroid replacement therapy as a rational strategy for treating disorders marked by neurosteroid-deficiency, such as CE and other related ovarian or menstrual disorders. In 2019, AP (renamed as brexanolone) was approved for treating PPD. A variety of synthetic neurosteroids are in clinical trials for epilepsy, depression and other brain disorders.

Recent advancements in our understanding of neurosteroids have entered a new era of drug discovery and one that offers a high therapeutic potential for treating complex brain disorders.



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