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🍽️ pronethalol hydrochloride non-drug

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  1. Beta-Adrenergic Blockade: Pronethalol hydrochloride acts by blocking beta-adrenergic receptors, which are found in various tissues throughout the body, including the heart, blood vessels, and lungs. By blocking the effects of adrenaline (epinephrine) and other catecholamines on these receptors, pronethalol hydrochloride can reduce heart rate, blood pressure, and myocardial contractility, thereby exerting antiarrhythmic and antihypertensive effects.

  2. Cardiovascular Effects: Pronethalol hydrochloride was initially studied for its potential use in the treatment of hypertension (high blood pressure), angina pectoris (chest pain), and cardiac arrhythmias (irregular heart rhythms). By reducing sympathetic nervous system activity and decreasing the workload on the heart, pronethalol hydrochloride can help manage these cardiovascular conditions. However, its use has largely been replaced by newer beta-blockers with improved selectivity and safety profiles.

  3. Side Effects: Like other beta-blockers, pronethalol hydrochloride can cause side effects related to its mechanism of action, including bradycardia (slow heart rate), hypotension (low blood pressure), fatigue, dizziness, and bronchoconstriction (narrowing of the airways). In addition, pronethalol hydrochloride has been associated with more serious adverse effects, including cardiac toxicity and hepatotoxicity (liver damage), which have contributed to its decreased use in clinical practice.

  4. Withdrawal: Abrupt discontinuation of pronethalol hydrochloride or other beta-blockers can lead to rebound hypertension, angina exacerbation, and potentially life-threatening arrhythmias. Therefore, it is important to taper the dose gradually under medical supervision when discontinuing treatment with pronethalol hydrochloride or transitioning to another beta-blocker.

  5. Historical Context: Pronethalol hydrochloride was one of the earliest beta-blockers to be developed and studied for clinical use. While it provided valuable insights into the potential therapeutic benefits of beta-adrenergic blockade, its limited selectivity and significant side effects ultimately led to its replacement by newer beta-blockers with improved efficacy and safety profiles.

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Data Contradictions β€” Limits of Certainity

Impacted of pronethalol hydrochloride non-drug On Probiotics

Rank Probiotic Impact
species Anaerobutyricum hallii Reduces
species Christensenella minuta Reduces
species Lacticaseibacillus paracasei Reduces
species Lactococcus cremoris Reduces

Bacteria Impacted by pronethalol hydrochloride non-drug

We extend modifiers to include items that changes the parent and child taxa. I.e. for a species, that would be the genus that is belongs to and the strains in the species.

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πŸ““ Direct Citations πŸ‘ͺπŸ‘Ά Indirect Citations Taxonomy Rank Effect
0 1 Ruminococcus genus Decreases
0 1 Coprococcus genus Decreases
0 1 Subdoligranulum genus Decreases
0 1 Wansuia genus Decreases
0 1 Agathobacter genus Decreases
0 1 Christensenella genus Decreases
0 1 Komagataeibacter genus Decreases
0 1 Butyrivibrio genus Decreases
0 1 Dorea genus Decreases
0 1 Maliibacterium genus Decreases
0 1 Odoribacter genus Decreases
0 1 Eubacterium genus Decreases
0 1 Anaerobutyricum genus Decreases
0 1 Catenibacterium genus Decreases
0 1 Treponema genus Decreases
0 1 Massilistercora genus Decreases
0 1 Novisyntrophococcus genus Decreases
0 1 Ligilactobacillus genus Decreases
0 1 Lacrimispora genus Decreases
0 1 Lacticaseibacillus genus Decreases
1 0 Ruminococcus bromii species Decreases
1 0 Coprococcus comes species Decreases
1 0 Agathobacter rectalis species Decreases
1 0 Odoribacter splanchnicus species Decreases
0 1 Dorea longicatena species Decreases
0 1 Coprococcus catus species Decreases
0 1 Blautia obeum species Decreases
0 1 Dorea formicigenerans species Decreases
0 1 Wansuia hejianensis species Decreases
0 1 Anaerobutyricum hallii species Decreases
0 1 Blautia sp. SC05B48 species Decreases
0 1 Lacrimispora saccharolytica species Decreases
0 1 Subdoligranulum variabile species Decreases
0 1 Ligilactobacillus ruminis species Decreases
0 1 Komagataeibacter oboediens species Decreases
0 1 [Ruminococcus] lactaris species Decreases
0 1 [Ruminococcus] torques species Decreases
0 1 Eubacterium ventriosum species Decreases
0 1 Clostridium sp. M62/1 species Decreases
0 1 Lachnoanaerobaculum gingivalis species Decreases
0 1 Christensenella minuta species Decreases
0 1 Blautia liquoris species Decreases
0 1 Clostridium sp. SY8519 species Decreases
0 1 Butyrivibrio crossotus species Decreases
0 1 Catenibacterium mitsuokai species Decreases
0 1 Faecalibacterium duncaniae species Decreases
0 1 Faecalitalea cylindroides species Decreases
0 1 Massilistercora timonensis species Decreases
0 1 Maliibacterium massiliense species Decreases
0 1 Treponema peruense species Decreases
0 1 Novisyntrophococcus fermenticellae species Decreases
0 1 Catenibacterium sp. co_0103 species Decreases
0 1 Qiania dongpingensis species Decreases
0 1 Faecalibacillus intestinalis species Decreases
0 1 [Clostridium] hylemonae species Decreases
0 1 Faecalibacterium sp. I2-3-92 species Decreases
0 1 Faecalibacterium sp. IP-3-29 species Decreases
0 1 Intestinibaculum porci species Decreases
0 1 Clostridium cadaveris species Decreases
0 1 Anaerostipes hadrus species Decreases
0 1 Pseudobutyrivibrio xylanivorans species Decreases
0 1 Lactococcus cremoris species Decreases
0 1 Lachnoclostridium phocaeense species Decreases
0 1 Marvinbryantia formatexigens species Decreases
0 1 Streptococcus suis species Decreases
0 1 Longicatena caecimuris species Decreases
0 1 Faecalibacterium sp. I3-3-89 species Decreases
0 1 Solibaculum mannosilyticum species Decreases
1 0 Lacticaseibacillus paracasei species Decreases
0 1 Lacticaseibacillus paracasei subsp. paracasei subspecies Decreases
0 1 Lacticaseibacillus paracasei subsp. tolerans subspecies Decreases

Impact of pronethalol hydrochloride non-drug on Conditions from US National Library of Medicine

A higher number indicates impact on more bacteria associated with the condition and confidence on the impact.

We have X bacteria high and Y low reported. We find that the modifier reduces some and increases other of these two groups. We just tally: X|reduces + Y|Increase = Positive   X|increases + Y|decrease = Negative.

Benefit Ratio:
Numbers above 0 have increasing positive effect.
Numbers below 0 have increasing negative effect.

Condition Positive Impact Negative Impact Benefit Ratio Impact
Abdominal Aortic Aneurysm 0.1 0.1
ADHD 0.7 0.5 0.4
Age-Related Macular Degeneration and Glaucoma 0.3 0.3
Allergic Rhinitis (Hay Fever) 0.2 0.2
Allergies 1.2 1.2 0
Allergy to milk products 0.9 0.2 3.5
Alopecia (Hair Loss) 0.2 0.2
Alzheimer's disease 1.3 1.4 -0.08
Amyotrophic lateral sclerosis (ALS) Motor Neuron 0.5 0.6 -0.2
Ankylosing spondylitis 0.1 0.6 -5
Anorexia Nervosa 0.5 0.8 -0.6
Asthma 0.2 0.1 1
Atherosclerosis 0.5 0.3 0.67
Atrial fibrillation 0.9 0.4 1.25
Autism 1.1 1.4 -0.27
Bipolar Disorder 0.5 0.7 -0.4
Brain Trauma 0.6 -0.6
Cancer (General) 0.1 0.1 0
Carcinoma 1.2 1.2 0
Celiac Disease 0.2 0.9 -3.5
Cerebral Palsy 0.5 -0.5
Chronic Fatigue Syndrome 1.1 2.6 -1.36
Chronic Kidney Disease 0.6 1 -0.67
Chronic Obstructive Pulmonary Disease (COPD) 0.2 0.3 -0.5
Coagulation / Micro clot triggering bacteria 0.1 0.9 -8
Cognitive Function 0.7 0.3 1.33
Colorectal Cancer 0.9 0.3 2
Constipation 0.5 0.5
Coronary artery disease 0.9 1 -0.11
COVID-19 1.1 3.3 -2
Crohn's Disease 1.4 1.9 -0.36
deep vein thrombosis 0.3 0.9 -2
Depression 1.4 2 -0.43
Eczema 0.1 -0.1
Endometriosis 0.4 0.8 -1
Epilepsy 0.3 0.1 2
Fibromyalgia 0.1 0.5 -4
Functional constipation / chronic idiopathic constipation 1 1.1 -0.1
gallstone disease (gsd) 0.6 0.1 5
Gastroesophageal reflux disease (Gerd) including Barrett's esophagus 0.5 -0.5
Generalized anxiety disorder 0.2 0.3 -0.5
Glioblastoma 0.1 0.1
Gout 0.5 0.2 1.5
Graves' disease 0.5 0.6 -0.2
Gulf War Syndrome 0.2 0.2
Halitosis 0.2 0.2
Hashimoto's thyroiditis 1.1 0.3 2.67
Heart Failure 0.9 1 -0.11
hemorrhagic stroke 0.2 0.2
High Histamine/low DAO 0.5 -0.5
hypercholesterolemia (High Cholesterol) 0.1 0.1
Hyperlipidemia (High Blood Fats) 0.1 0.1
hypertension (High Blood Pressure 1 1.1 -0.1
Hypothyroidism 0.1 0.4 -3
Hypoxia 0.1 0.1
IgA nephropathy (IgAN) 0.6 0.1 5
Inflammatory Bowel Disease 0.5 2.5 -4
Insomnia 0.6 0.6 0
Intelligence 0.2 0.3 -0.5
Intracranial aneurysms 0.5 0.3 0.67
Irritable Bowel Syndrome 1 1 0
ischemic stroke 0.5 0.1 4
Juvenile idiopathic arthritis 0.1 -0.1
Liver Cirrhosis 1.4 1.1 0.27
Long COVID 1.1 2.6 -1.36
Low bone mineral density 0.5 -0.5
Lung Cancer 0.8 -0.8
Mast Cell Issues / mastitis 0.7 -0.7
ME/CFS with IBS 1.3 -1.3
ME/CFS without IBS 0.2 0.5 -1.5
Menopause 0.2 0.2
Metabolic Syndrome 1.6 1.6 0
Mood Disorders 1.4 1.6 -0.14
Multiple Sclerosis 0.6 1.2 -1
Multiple system atrophy (MSA) 0.5 -0.5
myasthenia gravis 0.1 -0.1
neuropathic pain 0.2 -0.2
Neuropathy (all types) 0.1 0.2 -1
neuropsychiatric disorders (PANDAS, PANS) 0.1 0.1
Nonalcoholic Fatty Liver Disease (nafld) Nonalcoholic 1 1.7 -0.7
Obesity 2.1 1.8 0.17
obsessive-compulsive disorder 1.2 0.8 0.5
Osteoarthritis 0.4 0.8 -1
Osteoporosis 0.5 0.3 0.67
pancreatic cancer 0.1 0.1
Parkinson's Disease 1.8 1.6 0.13
Polycystic ovary syndrome 1.6 1.2 0.33
Postural orthostatic tachycardia syndrome 0.2 -0.2
primary biliary cholangitis 0.2 0.2
Primary sclerosing cholangitis 1.2 -1.2
Psoriasis 0.7 0.4 0.75
rheumatoid arthritis (RA),Spondyloarthritis (SpA) 1.9 0.8 1.37
Rosacea 0.6 0.6
Schizophrenia 1 0.8 0.25
scoliosis 0.4 0.5 -0.25
sensorineural hearing loss 0.3 0.3
Sjögren syndrome 0.1 0.4 -3
Sleep Apnea 0.9 0.2 3.5
Slow gastric motility / Gastroparesis 0.6 0.6
Small Intestinal Bacterial Overgrowth (SIBO) 0.3 0.3
Stress / posttraumatic stress disorder 0.2 0.2 0
Systemic Lupus Erythematosus 0.4 0.8 -1
Tic Disorder 0.6 0.5 0.2
Tourette syndrome 0.1 0.1
Type 1 Diabetes 0.7 0.8 -0.14
Type 2 Diabetes 1.9 1.3 0.46
Ulcerative colitis 0.4 1.1 -1.75
Unhealthy Ageing 0.4 0.8 -1
Vitiligo 0.6 0.3 1

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