Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Showing posts with label estrogen. Show all posts
Showing posts with label estrogen. Show all posts

Monday, September 14, 2026

Does estrogen protect against dementia? And if so, who should take it?

 Have your competent? doctor validate what should be done!

Do you prefer your doctor, hospital and board of director's incompetence NOT KNOWING? OR NOT DOING? Your choice; let them be incompetent or demand action!

Does estrogen protect against dementia? And if so, who should take it?

Recent research hints that systemic hormone replacement therapy for menopause may reduce the risk of dementia. But more data is needed to reach a definitive conclusion, experts told Live Science.

n women's reproductive years, their brains are exposed to high levels of sex hormones, and their neurons may come to depend on those hormones to function optimally. But leading up to and after menopause, the ovaries produce far less estrogen and progesterone, raising concerns that this drop in hormones may contribute to women's dementia risk.

"We think that the loss of those hormones at menopause renders those neurons more vulnerable to age-related cellular decline and pathologies like Alzheimer's," said Karyn Frick, a neuroscientist and professor of psychological and brain sciences at the University of Wisconsin-Milwaukee.

Wednesday, October 18, 2023

Stroke presents differently in women than men. Here are 7 symptoms to look for

FYI.

Stroke presents differently in women than men. Here are 7 symptoms to look for

People often say “time is money,” but talk to any neurologist and they’ll tell you time is brain. Because when it comes to strokes, every minute counts.

“The brain is very sensitive to injury,” said Dr. Eliza Miller, a neurologist at NewYork-Presbyterian/Columbia University Irving Medical Center. The human brain houses 86 billion neurons. For every minute that passes, a person having a stroke loses 1.9 million of them, according to research from the American Heart Association.

Quickly recognizing the signs of stroke is one of the best ways to save a life. BE-FAST is the go-to mnemonic for identifying a stroke. It stands for balance loss, eyesight changes, face drooping, arm weakness, speech difficulty and time to call 911. 

While BE-FAST helps with finding the most common symptoms of stroke, it may not reflect the stroke experience of all people. A growing body of research is now showing that women frequently present with atypical symptoms that are more subtle and vague, according to Dr. Hera Kamdar, an assistant professor of neurology at The Ohio State University Wexner Medical Center.

Stroke is the fifth leading cause of death in women, according to the US Centers for Disease Control and Prevention, and Kamdar believes unusual and overlooked symptoms are a contributor to the high mortality rate. Learning the signs could be the difference between making a full recovery and the worst-case scenarios: permanent disability or even death.

Overlooked signs of stroke in women

Beyond the symptoms listed in the BE-FAST mnemonic, Kamdar says some less noticeable signs of stroke seen in women include severe headache, generalized weakness, generalized fatigue, shortness of breath and chest pains, nausea and vomiting, brain fog and hiccups.

Kamdar said these symptoms appear suddenly, may be confused for another health issue, and may not present on only one side of the body (one-sided muscle weakness is common in people experiencing a stroke). Additionally, these symptoms would not improve over time.

Some symptoms on the list, like hiccups, might seem random at first glance. However, there is some research suggesting stroke-related hiccups may be a sign of brain damage to areas like the medulla oblongata, which controls breathing, and the supratentorial cortex, which is involved in the control of movement.

This doesn’t mean every woman should fear for her life every time they get the hiccups or feel drowsy. The symptoms become cause for concern when they are severe enough to impair your functionality, like feeling so weak and tired you are physically unable to get out of bed. Similarly, “every hiccup is not a stroke,” Kamdar said, but it becomes worrisome if it i hurting your throat or is in combination with other symptoms, such as vomiting.

Stroke symptoms in men vs. women

Scientists have come up with several theories for why men and women experience stroke differently. First, it’s all about hormones.

Estrogen is one of the main female reproductive hormones in the body, ongoing research shows it is protective against stroke. This may have to do with estrogen’s anti-inflammatory effects, which could protect against a brain injury. Estrogen also seems to help with increasing blood flow in the internal carotid artery, which supplies blood to the brain.

However, these hormonal benefits apply only to estrogen made in the body. Kamdar said taking synthetic forms of estrogen, whether through birth control or hormone replacement therapy, can actually increase the risk of stroke. Though the elevated risk remains small — 8.5 out of every 100,000 women will experience a stroke because of birth control.

“It’s not that people shouldn’t take birth control, it’s that people with other (stroke) risk factors shouldn’t use this type of contraceptive,” Miller added.

Age is another factor. Women also start making less estrogen as they get older, which could partially explain why the lifetime risk of stroke is higher in women than in men. Research suggests the substantial drop in estrogen levels during menopause is associated with an increased risk of stroke later in life. If women are outliving men, they also have more time and opportunity to have a stroke, Miller added.

Finally, pregnancy can triple the risk of stroke in young women, said Miller. This is because 10% of pregnant people in the United States develop a blood pressure condition called preeclampsia, which raises the risk of stroke.

“This is also true in the postpartum period, especially if the hypertension is not detected or not treated adequately,” Miller noted.

Another factor contributing to the high risk of stroke during pregnancy is blood clots. Miller said human blood has evolved to form blood clots — especially around the time of giving birth — to keep moms from bleeding to death during delivery.

Of course, not everyone who goes through pregnancy gets a blood clot, but Miller said “compared to someone who is not pregnant or postpartum, the risk is far higher during this time.”

What to do if you think you’re having a stroke

Both neurologists said the rate of recovery from stroke depends on how fast a person seeks help for themselves or a loved one. There are treatments available to improve the survival outcomes for stroke, Kamdar said, but they are all time sensitive.

Even if you’re unsure whether someone is having a stroke, Miller advised calling 911 anyway.

“I would rather have a person come into the emergency room and turn out to be completely fine than not come at all and we missed our opportunity to treat the stroke,” Miller said.

 

Monday, September 11, 2023

Exposure to Estrogen Linked to Less Brain Shrinkage in Midlife Women

With your brain atrophy post stroke you'll have to ask your doctor about this. 

 What is your doctor's protocol to prevent both brain and muscle atrophy?  No protocol, call the president and ask when competent persons will be hired.

Exposure to Estrogen Linked to Less Brain Shrinkage in Midlife Women

Summary: Longer and higher exposure to estrogen were associated with larger gray matter volume in middle-aged women.

Source: Alzheimer’s Research UK

A team of US-based researchers has found an association between indicators of longer estrogen exposure and reduced brain shrinkage in midlife women.

The findings are published today in the scientific journal, Neurology.

Previous research into the effects of estrogen on brain health has shown mixed results. Some studies have suggested that lower estrogen levels following menopause could be linked to brain aging and Alzheimer’s risk later in life.

The researchers looked at a total of 128 volunteers (99 women and 29 men), aged between 40 and 65 all with risk factors for Alzheimer’s disease, such as the APOE4 risk gene or a family history of the disease.

A range of reproductive history events were examined by questionnaires and interviews. These events included:

  • Whether participants had experienced menopause or a hysterectomy
  • The age they started periods
  • Their age at menopause
  • The length of time between the start of their periods and the start of menopause
  • The number of children and pregnancies they may have had
  • Whether they use menopausal hormone therapy (HT) and hormonal contraceptives (HC).

The researchers carried out brain scans to look specifically at areas called gray matter, including key regions that are damaged in Alzheimer’s disease. Lower volumes of gray matter have been linked to dementia risk and poorer brain health. All participants also had memory tests to assess their thinking and language skills.

Exposure to estrogen as a result of not having reached menopause, having more children and more reproductive years, and using HT and HC, was associated with larger gray matter volumes in midlife women.

Researchers found no association between reproductive history events and people’s memory scores, but people who scored better did have more gray matter compared to those that scored less.

This shows a model of a head and a brain
Previous research into the effects of estrogen on brain health has shown mixed results. Image is in the public domain

Dr. Sara Imarisio, head of research at Alzheimer’s Research UK, said: “Two thirds of people with dementia are women and while some of this difference is explained by women living longer, research has also implicated hormones like estrogen. The start of periods, having children, and menopause are significant events in many women’s lives and it’s important to understand how these biological changes might affect long-term brain health and dementia risk.

“This study linked exposure to estrogen to less brain shrinkage, an indication of lower dementia risk, but this is a small study, and it did not explain the causes for the association. The researchers worked with participants in midlife, a key period for brain health and reducing dementia risk, but as the brain scans were not specific to Alzheimer’s disease, we cannot make firm conclusions about risk of developing the condition from this study. Examining the biological pathways through which reproductive history influences cognitive aging and Alzheimer’s disease risk is the next step for researchers to understand this link.

“Alzheimer’s disease is caused by a complex mix of age, genetics and lifestyle factors—some of which are in our control to change, and others which aren’t. The best current evidence suggests that not smoking, only drinking within the recommended limits, staying mentally and physically active, eating a balanced diet, and keeping blood pressure and cholesterol levels in check can all help to keep our brains healthy as we age.”

About this brain aging research news

Author: Press Office
Source: Alzheimer’s Research UK
Contact: Press Office – Alzheimer’s Research UK
Image: The image is in the public domain

Original Research: Closed access.
“Association of Reproductive History With Brain MRI Biomarkers of Dementia Risk in Midlife” by Eva Schelbaum et al. Neurology

Thursday, February 2, 2023

Lifetime estrogen exposure linked to stroke after menopause

 FYI, ask your doctor what this means.

Lifetime estrogen exposure linked to stroke after menopause

Women in China may be at greater risk for stroke events following menopause, according to a study published in Neurology.

“Lifetime cumulative estrogen exposure due to reproductive factors could potentially be a useful indicator of patients’ risk of stroke events following menopause,” Leying Hou, PhD, of Zhejiang University School of Medicine in China, and colleagues wrote. “However, further research is needed on the underlying biological, behavioral and social mechanisms linking estrogen exposure with stroke risk across female patients’ lifespans.”

Woman with menopause
Lifetime cumulative exposure to estrogen was found to be associated with stroke events after menopause. Source: Adobe Stock

Researchers conducted a population-based, longitudinal, prospective cohort study using data from the China Kadoorie Biobank study to evaluate the link between lifetime cumulative estrogen exposure and stroke. They included 122,939 postmenopausal women, aged 40 to 79 years, without prior history of stroke from 2004 to 2008.

Hou and colleagues assessed cumulative estrogen exposure using reproductive lifespan (RLS), endogenous estrogen exposure (EEE) and total estrogen exposure (TEE).

During a median follow-up of 8.9 years, researchers identified 15,139 new-onset stroke cases, subcategorized as 12,853 ischemic stroke (IS), 2,580 intracerebral hemorrhage (ICH) and 269 subarachnoid hemorrhage (SAH), using health insurance data and a disease registry system.

According to results, compared with the lowest quartile of RLS, the highest quartile had a lower risk for total stroke (adjusted HR = 0.95; 95% CI, 0.92-0.98), IS (aHR = 0.95; 95% CI, 0.92-0.98) and ICH (aHR = 0.87; 95% CI, 0.81-0.94).

Further, when comparing the highest quartile with the lowest, EEE and TEE showed a graded association with descending risk for total stroke (EEE: aHR = 0.85; 95% CI, 0.82-0.89; TEE: aHR = 0.87; 95% CI, 0.84-0.9), IS (aHR = EEE: 0.86; 95% CI, 0.83-0.9; TEE: aHR = 0.86; 95% CI, 0.83-0.89) and ICH (EEE: aHR = 0.73; 95% CI, 0.65-0.81; TEE: aHR = 0.83; 95% CI, 0.76-0.91).

“Lifetime cumulative estrogen exposure due to reproductive factors, as indicated by RLS, EEE and TEE, is associated with stroke events among postmenopausal patients,” Hou and colleagues wrote. “For RLS, those in the highest quartile were found to have a lower risk of total stroke, IS and ICH. As for EEE and TEE, higher quartiles were found to have a graded association with a descending risk of total stroke, IS and ICH.”

Monday, April 25, 2022

Exposure to Estrogen Linked to Less Brain Shrinkage in Midlife Women

Ask your doctor what this means.

Exposure to Estrogen Linked to Less Brain Shrinkage in Midlife Women

Summary: Longer and higher exposure to estrogen were associated with larger gray matter volume in middle-aged women.

Source: Alzheimer’s Research UK

A team of US-based researchers has found an association between indicators of longer estrogen exposure and reduced brain shrinkage in midlife women.

The findings are published today in the scientific journal, Neurology.

Previous research into the effects of estrogen on brain health has shown mixed results. Some studies have suggested that lower estrogen levels following menopause could be linked to brain aging and Alzheimer’s risk later in life.

The researchers looked at a total of 128 volunteers (99 women and 29 men), aged between 40 and 65 all with risk factors for Alzheimer’s disease, such as the APOE4 risk gene or a family history of the disease.

A range of reproductive history events were examined by questionnaires and interviews. These events included:

  • Whether participants had experienced menopause or a hysterectomy
  • The age they started periods
  • Their age at menopause
  • The length of time between the start of their periods and the start of menopause
  • The number of children and pregnancies they may have had
  • Whether they use menopausal hormone therapy (HT) and hormonal contraceptives (HC).

The researchers carried out brain scans to look specifically at areas called gray matter, including key regions that are damaged in Alzheimer’s disease. Lower volumes of gray matter have been linked to dementia risk and poorer brain health. All participants also had memory tests to assess their thinking and language skills.

Exposure to estrogen as a result of not having reached menopause, having more children and more reproductive years, and using HT and HC, was associated with larger gray matter volumes in midlife women.

Researchers found no association between reproductive history events and people’s memory scores, but people who scored better did have more gray matter compared to those that scored less.

This shows a model of a head and a brain
Previous research into the effects of estrogen on brain health has shown mixed results. Image is in the public domain

Dr. Sara Imarisio, head of research at Alzheimer’s Research UK, said: “Two thirds of people with dementia are women and while some of this difference is explained by women living longer, research has also implicated hormones like estrogen. The start of periods, having children, and menopause are significant events in many women’s lives and it’s important to understand how these biological changes might affect long-term brain health and dementia risk.

“This study linked exposure to estrogen to less brain shrinkage, an indication of lower dementia risk, but this is a small study, and it did not explain the causes for the association. The researchers worked with participants in midlife, a key period for brain health and reducing dementia risk, but as the brain scans were not specific to Alzheimer’s disease, we cannot make firm conclusions about risk of developing the condition from this study. Examining the biological pathways through which reproductive history influences cognitive aging and Alzheimer’s disease risk is the next step for researchers to understand this link.

“Alzheimer’s disease is caused by a complex mix of age, genetics and lifestyle factors—some of which are in our control to change, and others which aren’t. The best current evidence suggests that not smoking, only drinking within the recommended limits, staying mentally and physically active, eating a balanced diet, and keeping blood pressure and cholesterol levels in check can all help to keep our brains healthy as we age.”

About this brain aging research news

Author: Press Office
Source: Alzheimer’s Research UK
Contact: Press Office – Alzheimer’s Research UK
Image: The image is in the public domain

 

Monday, November 15, 2021

Exposure to Estrogen Linked to Less Brain Shrinkage in Midlife Women

 I suppose you could ask your doctor what this means, have fun with that.

Exposure to Estrogen Linked to Less Brain Shrinkage in Midlife Women

 ummary: Longer and higher exposure to estrogen were associated with larger gray matter volume in middle-aged women.

Source: Alzheimer’s Research UK

A team of US-based researchers has found an association between indicators of longer estrogen exposure and reduced brain shrinkage in midlife women.

The findings are published today in the scientific journal, Neurology.

Previous research into the effects of estrogen on brain health has shown mixed results. Some studies have suggested that lower estrogen levels following menopause could be linked to brain aging and Alzheimer’s risk later in life.

The researchers looked at a total of 128 volunteers (99 women and 29 men), aged between 40 and 65 all with risk factors for Alzheimer’s disease, such as the APOE4 risk gene or a family history of the disease.

A range of reproductive history events were examined by questionnaires and interviews. These events included:

  • Whether participants had experienced menopause or a hysterectomy
  • The age they started periods
  • Their age at menopause
  • The length of time between the start of their periods and the start of menopause
  • The number of children and pregnancies they may have had
  • Whether they use menopausal hormone therapy (HT) and hormonal contraceptives (HC).

The researchers carried out brain scans to look specifically at areas called gray matter, including key regions that are damaged in Alzheimer’s disease. Lower volumes of gray matter have been linked to dementia risk and poorer brain health. All participants also had memory tests to assess their thinking and language skills.

Exposure to estrogen as a result of not having reached menopause, having more children and more reproductive years, and using HT and HC, was associated with larger gray matter volumes in midlife women.

Researchers found no association between reproductive history events and people’s memory scores, but people who scored better did have more gray matter compared to those that scored less.

This shows a model of a head and a brain
Previous research into the effects of estrogen on brain health has shown mixed results. Image is in the public domain

Dr. Sara Imarisio, head of research at Alzheimer’s Research UK, said: “Two thirds of people with dementia are women and while some of this difference is explained by women living longer, research has also implicated hormones like estrogen. The start of periods, having children, and menopause are significant events in many women’s lives and it’s important to understand how these biological changes might affect long-term brain health and dementia risk.

“This study linked exposure to estrogen to less brain shrinkage, an indication of lower dementia risk, but this is a small study, and it did not explain the causes for the association. The researchers worked with participants in midlife, a key period for brain health and reducing dementia risk, but as the brain scans were not specific to Alzheimer’s disease, we cannot make firm conclusions about risk of developing the condition from this study. Examining the biological pathways through which reproductive history influences cognitive aging and Alzheimer’s disease risk is the next step for researchers to understand this link.

“Alzheimer’s disease is caused by a complex mix of age, genetics and lifestyle factors—some of which are in our control to change, and others which aren’t. The best current evidence suggests that not smoking, only drinking within the recommended limits, staying mentally and physically active, eating a balanced diet, and keeping blood pressure and cholesterol levels in check can all help to keep our brains healthy as we age.”

About this brain aging research news

Author: Press Office
Source: Alzheimer’s Research UK
Contact: Press Office – Alzheimer’s Research UK
Image: The image is in the public domain

Original Research: Closed access.
“Association of Reproductive History With Brain MRI Biomarkers of Dementia Risk in Midlife” by Eva Schelbaum et al. Neurology

Tuesday, July 7, 2020

Estrogen as a Neuroprotectant in Both Sexes: Stories From the Bird Brain

10 posts on estrogen all the way back to Jan. 2012 just to show you how fucking incompetent your stroke medical world is.

 If your doctors and stroke hospital aren't getting human research going based on animal studies they don't belong in stroke at all. 

This line from rat testing should have immediately triggered human research;

Acute estrogen therapy during reperfusion improves tissue outcome from experimental stroke.

Estrogen as a Neuroprotectant in Both Sexes: Stories From the Bird Brain

  • Departments of Neuroscience, Biology, Psychology & The Center for Behavioral Neuroscience, American University, Washington, DC, United States
Estrogens such as estradiol (E2) are potent effectors of neural structure and function via peripheral and central synthesis. In the zebra finch (Taeniopygia guttata), neural E2 synthesis is among the highest reported in homeotherms due to the abundant constitutive expression of aromatase (E-synthase) in discrete neuronal pools across the forebrain. Following penetrating or concussive trauma, E2 synthesis increases even further via the induced expression of aromatase in reactive astrocytes around the site of damage. Injury-associated astrocytic aromatization occurs in the brains of both sexes regardless of the site of injury and can remain elevated for weeks following trauma. Interestingly, penetrating injury induces astrocytic aromatase more rapidly in females compared to males, but this sex difference is not detectable 24 h posttrauma. Indeed, unilateral penetrating injury can increase E2 content 4-fold relative to the contralateral uninjured hemisphere, suggesting that glial aromatization may be a powerful source of neural E2 available to circuits. Glial aromatization is neuroprotective as inhibition of injury-induced aromatase increases neuroinflammation, gliosis, necrosis, apoptosis, and infarct size. These effects are ameliorated upon replacement with E2, suggesting that the songbird may have evolved a rapidly responsive neurosteroidogenic system to protect vulnerable brain circuits. The precise signals that induce aromatase expression in astrocytes include elements of the inflammatory cascade and underscore the sentinel role of the innate immune system as a crucial effector of trauma-associated E2 provision in the vertebrate brain. This review will describe the inductive signals of astroglial aromatase and the neuroprotective role for glial E2 synthesis in the adult songbird brains of both sexes.
The effects of estrogens such as 17β-estradiol (E2) on the structure and function of the vertebrate central nervous system (CNS) are well known (1–6). These include organizational effects such as the masculinization and feminization of neural circuits perinatally (1, 5, 7), organizational and activational effects during adolescence [reviewed in (8)], and activational effects on a diverse set of physiological endpoints during adulthood including, but not limited to, reproductive and aggressive behaviors, cognition, mood, motor control, and mood [see (9)]. We have more recently learned that the influence of this steroid extends even further than the physiology of the normal brain and potently modulates many processes involved in pathological conditions such as traumatic brain injury (TBI).

Influence of E2 on the Injured Brain

Traumatic brain injury is defined in the clinical realm as a disruption in the normal function of the brain caused by percussive, concussive, or penetrating head injury. The incidence of TBI is strongly sexually dimorphic and male biased: a demographic characteristic attributed to higher rates of risky behavior in younger males [see (10) for review]. Following TBI, however, the predicted outcome and recovery of females are better than those of males (11). The underlying reason for this is hinted at by the observation that premenopausal women and those on hormone replacement have a lower risk of neurotraumatic events such as stroke, compared to the respective groups of age-matched men (12, 13). Following TBI in humans, both E2 and testosterone (T) decreased in the cerebrospinal fluid (CSF) over time. Importantly, a higher E2/T ratio was associated with lower mortality and better scores on the Glasgow Outcome Scale (GOS) 6 months after TBI (14). It is noteworthy that aromatase gene expression itself has been implicated in human TBI. More specifically, three single-nucleotide polymorphisms on the aromatase gene are associated with worse GOS-6 scores, suggesting that the expression of aromatase following TBI may be associated with differences in clinical outcomes post-TBI (14). The location of altered aromatase gene expression and the source of steroids in the CSF are unknown, but the pattern of data suggests the possibility that ovarian steroids may protect the brain from injury and/or damage and perhaps may even accelerate recovery.
Among the several steroids synthesized in the vertebrate ovary, E2 appears to be a powerful neuroprotectant as evidenced by multiple studies, using different types of TBI, in many vertebrate species. In rats, gerbils, and mice, females respond more favorably to medial carotid artery occlusion (MCAO) and other experimental inducers of ischemia (15–17). More recently, in mice subjected to controlled cortical impact, males demonstrated larger lesions compared to females (18). All these effects are apparently linked to circulating ovarian steroids because MCAO causes greater neural damage when it is conducted during metestrus compared to estrus, times of the rodent ovarian cycle when circulating E2 levels are low and high, respectively (15). In addition, infarct sizes increase following ovariectomy, and damage is exacerbated further the longer the animal is deprived of ovarian estrogens (19). The data demonstrate a neuroprotective effect of peripheral E2 across several species and types of damage. While it is true that all the aforementioned effects of E2 on the normal and injured brain reflect influences due to circulating levels of this steroid, there is excellent support for the notion that centrally synthesized E2 is a critical modifier of neurophysiological variables in both the normal and the injured CNS.

Thursday, December 13, 2018

Neuroprotective role of hypothermia in hypoxic-ischemic brain injury: combined therapies using estrogen

But is your doctor already treating you with testosterone? Would the combination of testosterone and estrogen cause problems?

Testosterone gel shown for first time to benefit men over 65

 

Testosterone Improves Woman’s Brain Functions

 

Low testosterone and the risk of dementia in elderly men

 

 

Neuroprotective role of hypothermia in hypoxic-ischemic brain injury: combined therapies using estrogen


Hypoxic-ischemic brain injury is a complex network of factors, which is mainly characterized by a decrease in levels of oxygen concentration and blood flow, which lead to an inefficient supply of nutrients to the brain. Hypoxic-ischemic brain injury can be found in perinatal asphyxia and ischemic-stroke, which represent one of the main causes of mortality and morbidity in children and adults worldwide. Therefore, knowledge on underlying mechanisms triggering these insults may help establish neuroprotective treatments. Selective Estrogen Receptor Modulators and Selective Tissue Estrogenic Activity Regulators exert several neuroprotective effects, including decrease of reactive oxygen species, maintenance of cell viability, mitochondrial survival, among others. However, these strategies represent a traditional approach of targeting a single factor of pathology without satisfactory results. Hence, combined therapies, such as the administration of therapeutic hypothermia with a complementary neuroprotective agent, constitute a promising alternative. In this sense, the present review summarizes the underlying mechanisms of hypoxic-ischemic brain injury and compiles several neuroprotective strategies, including Selective Estrogen Receptor Modulators and Selective Tissue Estrogenic Activity Regulators, which represent putative agents for combined therapies with therapeutic hypothermia.