Human microbial cells outnumber human somatic cells by a ratio of ten to one.
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Peer-reviewed literature and reference materials state that bacterial and microbial cells in the human body outnumber human somatic cells by approximately a factor of ten to one.
The human innate immune system is composed of functionally distinct modules that has evolved to provide different forms of protection against invading pathogens. The adaptive immune system provides long lasting pathogen specific immune responses. The innate immune system, though less specific to pathogens, serves as the body’s first line of defense against invading pathogens. The innate immune system is a conserved host response that entails the sensing of pathogen-associated molecular patterns (PAMPS) through germline-encoded pattern recognition receptors (PRRs), which initiate pathway-specific signaling networks, resulting in rapid responses that serve as the hosts’ first line of defense. Such germline encoded PRRs include but are not limited to Toll-like receptors (TLRs), RIG-I-Like (RLRS), NOD-like receptors (NLRs), and DNA receptors. PRRs are an irrefutable asset for the proper maintenance of human health. While they are traditionally known to recognize microbial molecules during infection scenarios, ligands for PRRs are not exclusive to foreign pathogens and are abundantly produced by the resident microbiota during normal colonization. ☐ The human microbiota consists of 10-100 trillion symbiotic microbial cells that reside in the body and vastly outnumber human somatic and germ cells. Microorganisms of the microbiota include bacteria, viruses, fungi, and protozoa. Together, these microbes form ecological communities in many anatomical sites. As such, the microbiota affe
Since the total number of microbial and viral cells in the human body (over 100 trillion) greatly outnumbers human cells (tens of trillions), there is considerable
Amphetamine is a central nervous system (CNS) stimulant that is used in the treatment of attention deficit hyperactivity disorder (ADHD) and narcolepsy; it is also used to treat binge eating disorder in the form of lisdexamfetamine. Historically, it has been used to treat nasal congestion and depression. Amphetamine is also used as an athletic performance enhancer and cognitive enhancer, and recre
As of December 2019, there is no effective pharmacotherapy for amphetamine addiction. Reviews from 2015 and 2016 indicated that TAAR1-selective agonists have significant therapeutic potential as a treatment for psychostimulant addictions; however, as of February 2016, the only compounds which are known to function as TAAR1-selective agonists are experimental drugs. Amphetamine addiction is largely mediated through increased activation of dopamine receptors and co-localized NMDA receptors in the nucleus accumbens; magnesium ions inhibit NMDA receptors by blocking the receptor calcium channel. One review suggested…
Acute amphetamine administration in humans increases endogenous opioid release in several brain structures in the reward system. Extracellular levels of glutamate, the primary excitatory neurotransmitter in the brain, have been shown to increase in the striatum following exposure to amphetamine. This increase in extracellular glutamate presumably occurs via the amphetamine-induced internalization of EAAT3, a glutamate reuptake transporter in some dopamine and norepinephrine neurons. This internalization is mediated by RhoA activation and its downstream effector ROCK, a process that is TAAR1-dependent. Amphetamine also induces the selective release of histamine from mast cells and efflux from histaminergic neurons through VMAT2. Acute amphetamine administration can also increase adrenocorticotropic hormone and corticosteroid levels in blood plasma by stimulating the hypothalamic–pituitary–adrenal axis.
In December 2017, the first study assessing the interaction between amphetamine and human carbonic anhydrase enzymes was published; of the eleven carbonic anhydrase enzymes it examined, it found that amphetamine potently activates seven, four of which are highly expressed in the human brain, with low nanomolar through low micromolar activating effects. Based upon preclinical research, cerebral carbonic anhydrase activation has cognition-enhancing effects; but, based upon the clinical use of carbonic anhydrase inhibitors, carbonic anhydrase activation in other tissues may be associated with adverse effects, such as ocular activation exacerbating glaucoma.
Since the total number of microbial and viral cells in the human body (over 100 trillion) greatly outnumbers human cells (tens of trillions), there is considerable
Adderall is the brand name of a fixed-dose combination medication used for the treatment of attention deficit hyperactivity disorder (ADHD) and narcolepsy. It is also used as an athletic performance enhancer, cognitive enhancer, appetite suppressant, and recreationally as a euphoriant. Such uses are illegal in many countries. It is a central nervous system (CNS) stimulant of the phenethylamine cla
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There are 10× more bacterial cells in our bodies from the microbiome than human cells. Viral DNA is known to integrate in the human genome, but the integration of bacterial DNA has not been described. Using publicly available sequence data from the human genome project, the 1000 Genomes Project, and The Cancer Genome Atlas (TCGA), we examined bacterial DNA integration into the human somatic genome. Here we present evidence that bacterial DNA integrates into the human somatic genome through an RNA intermediate, and that such integrations are detected more frequently in (a) tumors than normal sa
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