Multiple clinical and animal studies have revealed the changes in gut microbiota following ischemic stroke. One case-control study showed that the gut microbiota was significantly disrupted in patients with ischemic stroke and transient ischemic attack compared to controls. The main manifestations were the increase of opportunistic pathogens and the decrease of commensal or beneficial genera (Yin et al., 2015). In another study, the gut microbiota of ischemic stroke patients had more short chain fatty acids producer compared to healthy controls. In addition, it was found that the genus Enterobacter was significantly correlated with good outcomes (Li et al., 2019). An animal experiment based on the mouse middle cerebral artery occlusion (MCAO) model showed that ischemic stroke resulted in reduced species diversity and bacterial overgrowth of Bacteroidetes in the gut (Singh et al., 2016). Another study found that the levels of Bacteroidetes phylum and Prevotella genus were significantly increased in the gut of cynomolgus monkeys after MCAO, while Firmicutes phylum as well as Faecalibacterium, Oscillospira, and Lactobacillus genera were decreased, Oscillobacter, and Lactobacillus were decreased. In addition, intestinal mucosal damage was also observed (Chen et al., 2019c).

In addition to causing gut microbiota dysbiosis, ischemic stroke may also facilitate the translocation and dissemination of selective strains of bacteria that originated from the host gut microbiota. Infection is usually more likely to be observed after an ischemic stroke. Stanley et al. (2016) demonstrated that the microbial community in the lungs of post-stroke mice were derived from the small intestine of the host using high-throughput 16S rRNA gene amplicon sequencing and bioinformatics analyses.

Changes in gut bacteria can also be a factor in ischemic stroke. Significant microbiological disorders have been detected in inflammatory bowel disease (including Crohn’s disease and ulcerative colitis) and chronic kidney disease, all of which were found to be risk factors for ischemic stroke (Lee et al., 2010; Kristensen et al., 2014; Xiao et al., 2015). In addition, the composition of gut bacteria of people at high risk of stroke is also different from that of the normal population. Compared with the low-risk group of stroke, the levels of opportunistic pathogens among the people of high-risk group were found to be higher, and the difference of enterobacteriaceae was the most obvious. The people of low-risk group had higher concentration of butyrate-producing bacteria, such as Lachnospiraceae and Ruminococcaceae (Zeng et al., 2019). These findings may imply that disruption of microbial homeostasis in gut may precede the development of stroke. Therefore, it is feasible to predict and prevent stroke in advance by observing changes in intestinal flora.

There are also differences in gut microbiota among stroke patients of different ages. The incidence of stroke is closely related to age, with about 70–80% of ischemic strokes occurring in people over 65 years of age (Ovbiagele and Nguyen-Huynh, 2011), and age plays an important role in the development and prognosis of stroke (Yager et al., 2006; Manwani et al., 2011). Some pathophysiological processes are associated with aging, such as chronic inflammation and decreased immune function, can affect functional recovery after stroke and lead to poor prognosis in the elderly (Crapser et al., 2016; Ritzel et al., 2018). And On the other hand, the composition of gut microbes can be influenced by environment, disease and eating habits, as well as age and gender differences (Coman and Vodnar, 2020). The composition of the gut microbiota changes and the diversity diminishes as we get older. When the gut microbiome disorders, it has a detrimental effect on normal physiological activity and is also thought to affect age-related neurodegenerative diseases such as Alzheimer’s disease, Parkinson’s disease and Huntington’s disease (Mulak and Bonaz, 2015; Wasser et al., 2020; Escobar et al., 2022). Studies have shown that age plays an important role in the interaction between gut microbiota and stroke. Bacteroidetes and Firmicutes dominated the gut microbiota of both young and old adults. In older adults, the relative abundance of Firmicutes increased, and the content of SCFAs-producing bacteria and butyrate level decreased significantly (Biagi et al., 2010; Claesson et al., 2011), and intestinal permeability of the elderly was significantly higher than that of the young (Lee et al., 2020), which makes the older more susceptible to inflammatory response. And according to another study in mice, stroke outcomes can be improved in older mice by transplanting microbiota from younger mice. In contrast, after acquiring the microbiome of the older mice, the younger mice increased functional impairment after stroke (Spychala et al., 2018). In addition, age is an independent risk factor for post-stroke infection, the frequency and severity of infection after stroke were higher in the elderly. This may be related to the impaired integrity of the intestinal barrier, the entry of intestinal bacteria into peripheral tissues through the damaged barrier. And another possible explanation is intestinal inflammation. Higher levels of pro-inflammatory cytokines were detected in older patients than in younger patients (Crapser et al., 2016; Spychala et al., 2018; Blasco et al., 2020).

In addition, differences in the performance of gut microbiota after stroke also exist between genders. As two common intestinal bacteria, Bacteroidetes and Firmicutes, there are more Firmicutes detected in the males’ gut when they had a BMI of less than 33 compared with females. And when BMI is greater than 33, males have an advantage over females in the abundance of Bacteroidetes. In addition, the abundance of Lactobacilli in female is much higher than that in male (Haro et al., 2016). And there are also gender differences in post-stroke outcomes. In some studies, adult females have better recovery outcomes than males after stroke (Toung et al., 1998; Branyan and Sohrabji, 2020). And in middle age (45–55 years), male stroke patients have a higher mortality rate than female stroke patients (Redon et al., 2011). The prognosis of senile stroke women is proved significantly worse. This suggests that estrogen may play a protective role in the development of stroke. In addition, there were gender differences in the expression of bacterial metabolites after stroke. Fecal butyrate levels in male were significantly lower than in female after stroke (Ahnstedt et al., 2020), but LPS was found to be higher in male. After induced stroke, the male mouse model had greater intestinal permeability (Ahnstedt et al., 2020; El-Hakim et al., 2021). This suggests that male patients are more susceptible to intestinal microbiota translocation and post-stroke infection after stroke. There were also differences between male and female in inflammatory responses after stroke. Females expressed more Treg cells, while males had higher concentrations of CD8 + T cells (Jackson et al., 2019; Ahnstedt et al., 2020; Blasco et al., 2020). However, no more studies have clearly proved that gender can cause changes in the composition of intestinal microbiota in stroke patients, so the association between gender and stroke and intestinal microbiota needs further exploration.

The interaction between gut microbiota and ischemic stroke plays an important role in the occurrence, development and outcomes of stroke. We summarize the relevant pathophysiological mechanisms, including neuroendocrine pathways, bacterial metabolite, and immune response (Figure 1). The studies exploring this interaction and relevant mechanisms are listed in Table 1.

Gut-brain-microbiota axis plays an important role in gut microbiota-related stroke pathophysiology. There are several neural pathways for GBMAx communication, such as spinal and vagal pathways, autonomic nervous system (ANS), enteric nervous system (ENS), and hypothalamic-pituitary-adrenal (HPA) axis (Foster and McVey Neufeld, 2013; Carabotti et al., 2015). The function of gastrointestinal ANS will change after ischemic stroke. The production and release of norepinephrine is increased, and cholinergic activity is decreased, which results in altered intestinal mucin production, inhibiting intestinal activity and increasing intestinal permeability (Caso et al., 2009). This can affect the size and quality of the intestinal mucus layer. As the habitat of most intestinal microbiota, the change of the status of the mucus layer can affect the composition and function of the microbiota. Changes in intestinal permeability induced by stress would lead to the activation of glial cells and mast cells, increased production of interferon, and morphological changes of colonic epithelium. These changes are caused by the expression of reduced tight junction protein 2 and the occlusion of an important component of the intestinal tight junction (Demaude et al., 2006). Increased permeability of the intestinal epithelium will cause bacterial antigens to cross the intestinal epithelium and trigger an immune response, resulting in changes in intestinal flora and systemic effects (Yates et al., 2001). Thus, stroke-induced increases in intestinal permeability can be ameliorated after inhibition of β-adrenergic activity with β -blockers. It can also reduce the risk of bacteria spreading to surrounding organs (Stanley et al., 2016). HPA axis is also an important part of GBMAx and plays a role in enter-brain regulation. HPA axis regulates the body through the interaction of three endocrine glands, including hypothalamus, pituitary and adrenal, which can stimulate the release of steroid hormones such as cortisol under stress. Long-term elevation of serum cortisol can have toxic effects on the nervous system. Serum cortisol levels were found to be associated with stroke severity and post-stroke mortality (Christensen et al., 2004; Barugh et al., 2014). In addition, one study suggested that cortisol levels may be associated with gut microbiota diversity (Keskitalo et al., 2021). Interactions of gut microbiota and HPA axis may explain some severe mental disorders after ischemic stroke (Misiak et al., 2020).

Hormone levels are also thought to play a role in ischemic stroke. Deficiency of estrogen and other ovarian hormones was found to be a risk factor for ischemic stroke in post-menopausal women (Reeves et al., 2008). In animal experiments, different effects of estrogen on the prognosis and recovery of stroke rats were closely related to the age of the rats. Many studies demonstrated that neurological function in young female animals was less affected than in older animals after ischemic stroke. And in the same age groups, female animals showed better post-stroke neurological performance than males (Hall et al., 1991; Alkayed et al., 1998; Manwani et al., 2013). Estrogen can effectively prevent the growth of pathogenic bacteria, promote the growth and reproduction of beneficial bacteria, and maintain a reasonable composition of intestinal microbiota (Chen and Madak-Erdogan, 2016; Baker et al., 2017). There are significant differences in intestinal microbiome and metabolites between young and old women. Akkermansia muciniphila, for example, is a bacterium that can affect energy regulation, metabolism, and cardiovascular function (Everard et al., 2013; Plovier et al., 2017). In healthy mice, levels of Akkermansia muciniphila were found to be lower in female mice than in male mice. But after a stroke, its levels were significantly elevated in male mice (Stanley et al., 2018; Park et al., 2020). Estrogen therapy in stroke patients can reduce lipopolysaccharide (LPS) production and increase short-chain fatty acids (SCFAs) levels, which helps to inhibit inflammatory response and reduce brain tissue damage after ischemic stroke (Blasco-Baque et al., 2012; Wu et al., 2021). Transplanting fecal microbiome from young women undergoing estrogen therapy to older women with stroke effectively improved their functional outcomes (Park et al., 2020). However, estrogen therapy, which has a protective effect in younger women, increased the risk and severity of stroke in post-menopausal women (Wassertheil-Smoller et al., 2003; Selvamani and Sohrabji, 2010a,b). These studies suggested that estrogen levels could regulate intestinal microbiome homeostasis after ischemic stroke and influence stroke outcomes. But more research is needed to explore the relationship between hormones, age, gut microbiota, and ischemic stroke.

Gut microbiota plays an important role in the production and secretion of over 100 metabolites. However, the role of these metabolites in neurological function after ischemic stroke has not been fully studied (Bostanciklioğlu, 2019). SCFAs are the main product that produced by gut microbiota through fermentation of dietary fiber, including acetate, propionate, and butyrate. Recent studies suggested that anaerobic bacteria, such as Firmicutes, produced a great amount of SCFAs by fermenting dietary fiber (Nakamura et al., 2017). SCFAs can also be produced by fermentation of proteins and amino acid, and about 1% of E. coli bacteria can produce branched SCFAs (such as isobutyric and isovaleric acids) through this pathway (Smith and Macfarlane, 1997; Louis and Flint, 2017). In addition, acetyl-CoA formed by glycolysis can also be converted to butyric acid by the action of Butyryl-CoA: Acetate-CoA transferase (Duncan et al., 2002). Moreover, SCFAs produced by different species of bacteria also varies. For instance, acetate is metabolized by enteric and acetogenic commensal bacteria (Maa et al., 2010). Propionate is the main metabolite of bacteroides and Firmicutes (Zapolska-Downar and Naruszewicz, 2009). Eubacterium, anaerobe and Faecalis are the main bacteria which produce butyrate (Zapolska-Downar et al., 2004).

Short-chain fatty acids have positive effects on human intestinal function, such as enhancing intestinal motility, reducing inflammatory cell level, and regulating intestinal hormones and neuropeptide levels (Silva et al., 2020). SCFAs are also important for cerebral development and maintenance of normal function of the central nervous system (CNS). They can cross the BBB, and are essential for several processes, such as microglial maturation, intestinal neuron stimulation of ANS, and mucosal serotonin secretion (Braniste et al., 2014; Erny et al., 2015). In addition, SCFAs also play an immunomodulatory role. They can induce T cells to differentiate into effector cells and regulatory cells according to the immune environment (Park et al., 2015).

In the early stage of ischemic stroke, the levels of acetic acid and propionic acid were found to be significantly lower than normal. The concentrations of isobutyric acid and isovaleric acid were increased in the early stage but low in the later stage. Butyric acid and valeric acid were deficient in both early and later stages of ischemic stroke (Chen et al., 2019b). This difference may be related to different metabolic pathways required to produce different SCFAs. Studies have demonstrated that SCFAs have a neuroprotective effect. The lower the concentration of acetic acid, valeric acid, especially butyric acid, in stroke patients, the greater the volume of cerebral infarction and the worse the neurological function score (Chen et al., 2019b). Oral infusion of SCFAs-producing bacteria and inulin reduced neurological deficits and improved post-stroke depression-like behavior in elderly mice (Lee et al., 2020). Butyrate has the function of reducing neurotoxicity, alleviating neuroinflammation, and relieving behavioral disorders. Intestinal butyrate supplementation can improve the level of neurological recovery after brain injury and reduce the volume of cerebral infarction. It was also effective in reducing cerebral edema, lowering blood lipid levels, and reducing the risk of thrombosis (Sharma et al., 2015; Patnala et al., 2017). Butyrate can regulate immune function by inhibiting histone deacetylase (HDAC) and mammalian target of rapamycin (mTOR) signal in circulating leukocytes. Studies have shown that higher concentrations of butyrate in feces or intravenous butyrate solution can enhance the antimicrobial activity of monocytes and macrophages and increase the body’s resistance to pathogens (Chakraborty et al., 2017; Haak et al., 2018).

Trimethylamine N-oxide (TMAO) is a kind of metabolic product of gut microbiota, mainly derived from the dietary nutrients rich in phosphatidylcholine, choline, and L-carnitine. First, Gut microbes metabolize foods such as eggs and beef to produce the intermediate trimethylamine by the activity of trimethylamine (TMA) lyases. In the second step, TMA is oxidized to TMAO by hepatic flavin-containing monooxygenases (Bennett et al., 2013). TMAO can induce atherosclerosis by increasing uptake of cholesterol in macrophages and promoting foam cell formation (Wang et al., 2011), enhance platelet hyperresponsiveness and increases the risk of thrombosis by changing stimulus-dependent calcium signal (Zhu et al., 2016). Higher concentrations of TMAO were found to be associated with an increased risk of cardiovascular events (Wang et al., 2011; Koeth et al., 2014; Tang et al., 2014). In addition, high levels of plasma TMAO have been shown to reduce long-term survival in patients with chronic kidney disease (Tang et al., 2015). Notably, a study of TMAO and cardiovascular disease risk in hemodialysis patients showed a significantly higher risk of death in white patients than in blacks (Shafi et al., 2017). This suggests that the effects of TMAO may differ across racial and ethnic groups.

According to the current study, TMAO can aggravate brain injury after ischemic stroke through a variety of pathophysiological processes. In addition to accelerating atherosclerosis and enhancing thrombogenesis potential, it can also promote vascular inflammation and endothelial dysfunction (Seldin et al., 2016; Boini et al., 2017; Li T. et al., 2017). TMAO also increases oxidative stress, enhances mitochondrial damage, and inhibits mTOR signaling, thereby impairing neural function (Chen et al., 2017; Li D. et al., 2018). TMAO is also a risk factor for hypertension and diabetes, which are linked to ischemic stroke. TMAO levels will rise and then decrease gradually over time after stroke onset. High concentrations of TMAO in patients with early onset are often associated with poor prognosis. Therefore, the measurement of plasma concentrations of gut microbial TMAO in stroke patients is helpful for us to predict the prognosis of patients (Tan et al., 2020; Zhang J. et al., 2019).

As a gathering place of immune cells, gastrointestinal tract affects the growth and development of immune cells and plays an important role in regulating immune response (Li et al., 2019). After ischemic stroke, both local neuroinflammatory responses and peripheral immune responses can be activated (Chamorro et al., 2012). It is found that different kinds of immune cells can aggravate the injury or protect the damaged brain tissue, respectively.

After the occurrence of stroke, activation of cerebral resident immune cells such as microglia, astrocytes, neutrophils and macrophages increase the production of pro-inflammatory cytokines, chemokines, proteases, and adhesive proteins (Iadecola and Anrather, 2011; Yang et al., 2019). The activation of inflammatory cells destroys the integrity of BBB, increases the chemotaxis of inflammatory cytokines in cerebral ischemia area, aggravates the damage of brain tissue. Experimental studies have shown that endotoxins metabolized by microbiota, such as LPS, can exacerbate neuroinflammation either directly or by inducing migration of peripheral immune cells to the brain (Lukiw et al., 2018). And raising LPS levels in stroke mice can promote the production of inflammatory factors like interleukin (IL)-6 and tumor necrosis factor (TNF)-α, affects BBB function, increase the neurological impairment, aggravating cerebral edema and reduce life expectancy of the mice (Dénes et al., 2011). It also led to increased plasma levels of pro-inflammatory cytokines that may promote dysregulation of the gut microbiome (Yamashiro et al., 2017). The dysbiosis of intestinal microflora can further increase the production of peripheral inflammatory cytokines. These cytokines can cross the BBB and exacerbate brain ischemic injury (Liu et al., 2020). Rapid dysregulation of intestinal flora in the first 24 h after stroke can promote cerebral infarction through inflammatory response. By inhibiting the overgrowth of Enterobacteriaceae and other opportunistic pathogens in stroke patients, systemic inflammation and cerebral infarction can be effectively reduced (Xu et al., 2021).

Peripheral immune inflammatory cells are involved in the cerebral immune inflammatory response following ischemic stroke and play an important role in the process of brain injury and tissue repair. The main cells involved in the human immune system are B lymphocytes, T lymphocytes, MHC and effector cells (Flajnik and Kasahara, 2010). In ischemic stroke, impaired BBB promotes T infiltration and interferon (IFN)-γ accumulation (Kleinschnitz et al., 2010; Liesz et al., 2011). In animal stroke models, T cell and B cell counts in Peyer’s patches decreased within 24 h, and activated T lymphocytes migrate from the Peyer patches of the small intestine or from the intestinal lamina propria to the brain within 2–3 days after stroke, where they primarily located in is leptomeninges (Schulte-Herbruggen et al., 2009). T cells can affect the secretion of cytokines IL-17 and IL-23 (Fan et al., 2020), lead to chemokine production and increased infiltration of cytotoxic cells (neutrophils and monocytes) into brain tissues, and then results in neurotoxic effects on ischemic lesions, resulting in increased infarct volume. Experiments have shown that inhibition of T lymphocyte invasion can effectively reduce the infarct size after stroke (Liesz et al., 2011). Conversely, upregulation of T regulates cell (Treg) level or increases IL-10 concentration can inhibit the production of proinflammatory mediators, thereby reducing the volume of cerebral infarction (Wei et al., 2011; Bodhankar et al., 2015). Similarly, regulatory B lymphocytes may also play a protective role in ischemic stroke by regulating anti-inflammatory factors such as IL-10 and transforming growth factor (TGF)-β (Doyle et al., 2015). Increasing B cell concentration in the brain can reduce infarct volume after stroke (Chen et al., 2012).

Intestinal microbiome dysregulation can reduce systemic anti-inflammatory cytokines such as TGF-β and IL-10 (Yan et al., 2009; Benakis et al., 2016). As a bacterial metabolite, SCFAs can act on immune cells by inhibiting histone deacetylase (HDAC) or by acting as a ligand for G-protein-coupled receptors. After stroke, SCFAs also stimulates the production of colonic Treg cells by producing IL-10 cytokines and TGF-β, and expressing Foxp3 and cell surface markers CD4 and CD25, thereby reducing infarct size (Sadler et al., 2020). In addition, monocytes/macrophages in the intestinal tract of stroke patients can be activated by intestinal flora. Intrusions of intestinal monocytes into the brain can be detected during the acute phase of stroke. Therefore, monocytes/macrophages also play a role in microbiome mediated stroke prognosis (Singh et al., 2016).

Post-stroke infection is an important factor causing worsen outcomes of stroke patients, and more than one-third of patient’s condition and treatment are complicated by post-stroke infection complications (Emsley and Hopkins, 2008). Increased susceptibility to infection after ischemic stroke is associated with activation of feedback activity between the CNS and peripheral immune organs (Chamorro et al., 2012). And according to current studies, the increased permeability and dysfunction of the intestinal barrier after stroke can cause bacterial migration and spread of the intestinal microbiome, which may be one of the mechanisms of post-stroke infection (Figure 1; Stanley et al., 2016).

After ischemic stroke, the sympathetic nervous system is activated, the intestinal permeability is increased, the intestinal barrier is damaged, and the antibacterial function of the body is reduced. These changes promote the transfer of bacteria to extra-intestinal organs, blood or lymph, participates in local and systemic immunity, and may lead to organ infections and even sepsis (Hagiwara et al., 2014). The β-adrenergic signaling pathway may play an important role (Wong et al., 2011). When β-adrenergic receptors are blocked, the integrity of the intestinal barrier can be inhibited. For example, feeding stroke mice with propranolol can’t completely avoid the occurrence of infection, but can obviously reduce the serious situation of systemic tissue infection after ischemic stroke (Stanley et al., 2016).

In an mice experimental study, germ-free mice were modeled by two methods. The results showed that the intestinal microbiota of mice with post-filament middle cerebral artery occlusion model (fMCAo) had significantly imbalance and the diversity was decreased while those in mice with permanent distal middle cerebral artery occlusion model (cMCAo) had relatively little influence. This suggests that the changes in microbiome are secondary to the stroke and the degree of disturbance is affected by the severity of stroke (Singh et al., 2016).

In turn, gut microbiota disturbance may be one of the important causes of enterogenic infection, sepsis even multiple-organ dysfunction syndromes (MODS) (Lyons et al., 2016; Haak and Wiersinga, 2017). After stroke, the destruction of the integrity of the intestinal barrier provides conditions for bacterial migration. Although in healthy individuals a variety of gut microbiomes are also found in blood and lung tissue (Potgieter et al., 2015; Dickson et al., 2016; Li Q. et al., 2018). However, due to the destruction of the integrity of the intestinal barrier, pathologic translocation of intestinal bacteria in stroke patients increases, leading to an increase in the incidence of post-stroke infection (Tascilar et al., 2010).

Bacterial pneumonia is the most common complication of ischemic stroke patients and one of the early nosocomial infections (Langhorne et al., 2000; Hannawi et al., 2013). Blood or sputum culture samples taken from patients with stroke complicated with pneumonia are often absent of the common pathogens that cause pneumonia, or have much less than those found in patients with common pneumonia (Marik, 2001). In one study, prophylaxis with antibiotics in ischemic stroke patients did not reduce the incidence of pneumonia or death compared with untreated patients (Kalra et al., 2015). In contrast, evidence from several studies suggests that post-stroke pneumonia is associated with the transmission of certain bacteria from the patient’s gut microbiota. These bacteria, when translocated, become pathogenic strains (Stanley et al., 2016). This suggests that endogenous factors play a more important role in the onset of post-stroke pneumonia than exogenous infection. Changes in intestinal permeability after ischemic stroke can induce bacterial migration and infection. In addition to direct transmission through the small intestine after, gut bacteria can also travel through the portal vein to the liver, where they can spread indirectly to the lungs after filtering through the blood.

Neuropsychiatric disorders are also common complications of stroke, includes depression, anxiety, mania, dementia, and cognitive impairment (Hackett et al., 2014; Hackett and Pickles, 2014). About one-third of patients experience cognitive impairment within a year of a stroke (Li X. et al., 2017). Gut microbiota dysbiosis can be found in many neurological disorders such as Alzheimer’s disease and depression (Cho et al., 2021). The high-abundance Prevotella group expressed more negative emotions and reduced hippocampal functional activation than the group with higher levels of bacteroides (Tillisch et al., 2017). In addition, bacterial metabolites have been linked to cognitive function. Ischemic stroke patients who detect higher levels of TMAO experience more severe cognitive impairment (Zhu et al., 2020). SCFAs producing bacteria (such as Lachnospiraceae and Ruminococcus) were significantly reduced in patients with amnestic cognitive impairment (Liu et al., 2021). Another study found similar results. The abundance of Lachnospiraceae, Clostridiaceae, and Ruminococcus was reduced in the high-risk group compared with the low-risk group (Huang Q. et al., 2021). Gut microbiota may aggravate neuropsychiatric symptoms by common pathogenesis, like neuroinflammatory response. These results suggest that it is feasible to predict the occurrence of cognitive impairment after ischemic stroke by intestinal flora.

Current studies on the gut-brain axis mainly focus on patients with ischemic stroke. Compared with ischemic stroke, there are fewer clinical and experimental studies on the association between hemorrhagic stroke and intestinal flora. The occurrence probability of intracranial hemorrhage (ICH) and subarachnoid hemorrhage (SAH) are less than that of cerebral infarction, but the mortality and disability rate of ICH and SAH are not low. Although the pathogenesis and clinical manifestations of the two types of stroke patients are different, similar results of microbiome disruption were found between the two stroke patients. Some studies have even shown that the stability disruptions of gut microbiota in patients with hemorrhagic stroke or high NIHSS scores are more severe than those with ischemic stroke and TIA (Zeng et al., 2019; Haak et al., 2021). Like ischemic stroke, some mechanisms of action are also at work in ICH patients. According to a case-control study of hypertension patients in China, intestinal bacterial metabolite TMAO levels are strongly associated with stroke. The association between TMAO and hemorrhagic stroke was significantly higher than that of ischemic stroke (Nie et al., 2018). TMAO has also been shown to be closely associated with the prognosis of ICH patients (Zhai et al., 2021). Inflammation has also been found to play an important role in the brain-gut axis in patients with intracerebral hemorrhage. An animal study has demonstrated that dysregulation of gut flora is associated with dysregulation of pro-inflammatory T cell differentiation in mice after intracerebral hemorrhage, which exacerbates neuroinflammatory responses and causes secondary damage to brain tissue. Neuroinflammation was reduced in ICH mice after intestinal transplantation with fecal gut microbiota from healthy mice (Yu et al., 2021). Intestinal disruption also occurred after ICH. Persistent ileal mucosal injury and increased intestinal permeability were observed in ICH mice. This permeability reached its highest level on the 7th day after intracerebral hemorrhage. Intestinal disruption also occurred after ICH. Persistent ileal mucosal injury and increased intestinal permeability were observed in ICH mice. This permeability reached its highest level on day 7 of intracerebral hemorrhage. Intestinal bacteria can enter the blood circulation through the broken intestinal mechanical barrier, and lead to systemic inflammation, especially pneumonia (Zhang H. et al., 2021).

As the most common cause of SAH, intracranial aneurysms have a prevalence of about 3% in the population and are associated with 80–85% of non-traumatic SAH (Kassell et al., 1990; Vlak et al., 2011). The current study reveals a partial link between intracranial aneurysms and gut microbiota. Destruction of the gut microbiota by antibiotics can reduce the incidence of intracranial aneurysms in mice (Shikata et al., 2019). And in another study, intracranial aneurysm formation can be induced in normal mice after transplantation of feces from patients with an intracranial aneurysm. Further studies revealed a relationship between aneurysms and the abundance of H. hathewayi in the gut (Li H. et al., 2020). This is a group of anaerobic bacteria that can maintain stable levels of serum taurine, which reduces the risk of aneurysm formation and rupture by inhibiting systemic inflammation. Meanwhile, artificial taurine supplementation also reversed the progression of intracranial aneurysms (Li H. et al., 2020). On the other hand, intestinal microbiota can also play an important role in the rupture of aneurysms. Compare the gut microbiota of patients with ruptured aneurysms (RA) and unruptured aneurysms (URA), researchers found that the genus Campylobacter and C. ureolyticus were significantly increased in the RA group patients (Kawabata et al., 2022). This may be related to the more intense inflammatory response and the remodeling or destruction of blood vessel walls induced by Campylobacter (Nilsson et al., 2018; Kushamae et al., 2020).

Cavernous hemangioma (CA) is also a kind of common vascular disorder will cause cerebral hemorrhage. More abundance Gram-negative bacteria O. splanchnicus and lower levels of gram-positive bacteria F. prausnitzii and B. adolescentis can be found in CA patients, compared with the non-CA patients. However, the most valuable combination of bacteria for diagnosing disease and assessing its severity was not found in this experiment. This indicates that the influence of bacteria on CA is not independent but may play a role together with other factors.

Currently, it has been proved that there is a correlation between intestinal microbiota dysbiosis after stroke and the incidence and progression of stroke. Therefore, it is feasible to predict the disease recovery of patients by indicators related to intestinal microbiome. By comparing samples from stroke patients and control group, several studies got the similar conclusions that stroke patients had a reduction in Firmicutes and Bacteroidetes, while the abundance of Proteobacteria was increased. And the difference of composition ratio in the microbiome was correlated with the severity of the disease. The abundance of TMA-producing bacteria was significantly higher, and the levels of intestinal butyrate-producing bacteria decreased in severe patients compared with mild patients. And the metabolites like TMA or butyrate of these bacterias also had a similar situation (Gu et al., 2021; Haak et al., 2021; Xia et al., 2021).

By examining the difference in intestinal microbiota distribution between acute ischemic stroke patients and healthy participants, a study established a Stroke Dysbiosis Index (SDI), as an independent predictor of severe disease (NIHSS > 8) and poor prognosis (MRS > 2) (Xia et al., 2019). Increased abundance of Enterobacteriaceae and Parabacteroides have a correlation with a higher SDI, while the abundance of fecalibacterium, Clostridiaceae, and Lachnospira decreased. In addition, animal studies have shown that mice that received fecal transplants from patients with a high SDI index experienced severe brain damage, increased levels of IL-17 and T cells, and a significantly higher risk of stroke than mice that received normal fecal transplants.