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Acne causes upper respiratory tract infections - fact or myth

Homepage Articles Acne causes upper respiratory tract infections - fact or myth

Acne causes upper respiratory tract infections - fact or myth

Milk and dairy products (the word cow's milk) have been studied many times and from different angles. However, uncertainties, half-truths, and puzzles about milk and milk products in the context of their impact on infections, especially those of the respiratory system, continue to spread. According to FAO, the world's dairy production is growing steadily. WHO, as well as the authors of the Polish guidelines recommend that dairy be included in the daily diet. Time to clarify what has a specific scientific basis, and what is a myth and should be debunked.

Table of Contents

1. It's got ingredients and properties

Additionally fermented dairy products, i.e. kefir, yogurt and buttermilk, therefore provide milk fermentation bacteria or probiotics. Their beneficial anti-health effects have been confirmed in studies (A. Rock 2018; D.R. Khare, G. Cow's milk contains 2,54, 2% proteins with a number of health effects. The second group consists of whey protein: β-lactoglobulin, α-lactoalbumin, single-celled cow's whey albumin, which has a higher immunoglobulin value (I.Case has been shown to have a lower anti-hypertensive effect on blood levels, two anti-inflammatory amino acids, anti-phosphoric acid family, and anti-bacterial proteins). In addition to the ability to use iron compounds in whey and lactose, this group also has anti-oxidant properties. In addition, it has the potential to reduce the effects of protein and protein-resistant agents, such as chlorophyllum and chlorophylls, as well as its anti-cholinergic effects on the body's immune system,

2. Upper respiratory tract infections effects of nausea

In one study, it was shown that the molecules contained in raw cow's milk may also locally differentiate the Treg lymphocytes responsible for counteracting the overly severe immune response of people who have developed an infection-causing micro-organism attack or stimulate the immune system to work (O. When the immune response is modified, the mucous membrane is strengthened, and the intestinal barrier is reinforced). However, this factor may locally create conditions that facilitate resistance to infection by individuals who have too severe immune responses. However, a very large and important anti-inflammatory group (IgG) appears to have a significantly reduced effect on the functioning of immunoglobulin-dependent pathogenic pathogens (i.e. ulcerative cell carcinogenesis) (N.G. Saad and other experiments conducted between 2016 and 2016). According to the results of these studies, the effects of these bacteria on the body's immune system may also be influenced by a number of studies conducted in 2018 (a study conducted by Dr. Dr. Tim Jones and Dr. M. C. W

3. Increased mucus excretion in the upper respiratory tract

However, in one study, the authors concluded that the sensation of increased saliva secretion in the upper respiratory tract was not caused by milk. Participants in the experiment were given milk and a soybean drink. It is likely the result of a combination of an emulsion such as milk (and a soda drink having similar properties) with saliva and its thickening in the oral cavity. However, the researchers note that the feeling of an enlarged saliva was reported by those who participated in the test (e.g. the results of an allergy test in a single person who was infected with this disease or a viral infection that may have spread as a result of an excess of saliva). However, it was observed that in 2005 there was a significant increase in the number of reactions to oral and nasal diseases such as cataracts and cataract infections in the nose and nose, as well as in 2005 that they were observed to be associated with an increase in blood pressure and blood pressure in the nasal cavities.

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Bordoni A. et al., Dairy products and inflammation: A review of the clinical evidence, „Critical Reviews in Food Science and Nutrition” 2017, 57(12), 2497–2525.
Fardet A., Rock E., In vitro and in vivo antioxidant potential of milks, yoghurts, fermented milks and cheeses: a narrative review of evidence, „Nutrition Research Reviews” 2018, 31(1), 52–70.
Khare A., Smriti G., Cholesterol-Lowering Effects of Lactobacillus Species, „Current Microbiology” 2020, 77(4), 638–644.
Krauze A., Alergia na białko mleka krowiego–postacie kliniczne, „Alergia Astma Immunologia” 2015, 20(1), 12–16.
Michael D.R. et al., A randomised controlled study shows supplementation of overweight and obese adults with lactobacilli and bifidobacteria reduces bodyweight and improves well-being, „Scientific Reports” 2020, 10(1), 4183.
Perdijk O. et al., Cow’s Milk and Immune Function in the Respiratory Tract: Potential Mechanisms, „Frontiers in Immunology” 2018, 9, 143.
Radkowska I., Identyfikacja i właściwości prozdrowotne mleka zawierającego beta-kazeinę typu A2, „Roczniki Naukowe Zootechniki” 2020, 47(2), 165–177.
Saad K. et al., Effects of bovine colostrum on recurrent respiratory tract infections and diarrhea in children, „Medicine” 2016, 95(37), 4560.
Shearer Z., Jones S.M., Consumption of Unprocessed Cow’s Milk Protects Infants From Common Respiratory Infections, „Pediatrics” 2015, 136(sup 3), 226–227.
Timby N. et al., Infections in Infants Fed Formula Supplemented With Bovine Milk Fat Globule Membranes, „Journal of Pediatric Gastroenterology and Nutrition” 2015, 60(3), 384–389.
Wüthrich B. et al., Milk consumption does not lead to mucus production or occurrence of asthma, „Journal of the American College of Nutrition” 2005, 24(sup 6), 547–555.