D1 - Human Nutrition Flashcards
Nutrient
chemical substance found in foods that is used in the human body
carbohydrates, proteins, lipids, vitamins, minerals and water
Essential nutrients
cannot be synthesised by the body and must be ingested as part of the diet
Non-essential nutrients
Non-essential nutrients can be made by the body or have a replacement nutrient which serves the same dietary purpose
Carbohydrates are not considered essential nutrients as human diets can obtain energy from other sources without ill effect
Malnutrition
health condition caused by a deficiency, imbalance or excess of nutrients in the diet
It can be caused by an improper dietary intake of nutrients – e.g. overnutrition (too much) or undernutrition (not enough)
It can be caused by the inadequate utilisation of nutrients by the body – e.g. due to illness or disease
Malnutrition symptoms
stunted growth and wasting (undernutrition), as well as obesity (over nutrition)
Energy content
estimated by burning a sample of known mass and measuring the energy released via calorimetry
Energy (joules) = Mass of water (g) × 4.2 (J/gºC) × Temperature increase (ºC)
Errors in calorimetry
biggest source of error in calorimetry is usually caused by the unwanted loss of heat to the surrounding environment
The food sources should be burnt at a constant distance from the water to ensure reliability of results
The initial temperature and volume of water should also be kept constant (1 g of water = 1 cm3 or 1 ml)
Energy content - carbs
Carbohydrates are preferentially used as an energy source because they are easier to digest and transport
Energy content - lipids
Lipids can store more energy per gram but are harder to digest and transport (hence are used for long-term storage)
Energy content - proteins
Protein metabolism produces nitrogenous waste products which must be removed from cells
Amino acids
20 different amino acids which are universal to all living organisms
Essential amino acids cannot be produced by the body and must be present in the diet
Non-essential amino acids can be produced by the body and are therefore not required as part of the diet
Conditionally non-essential amino acids can be produced by the body, but at rates lower than certain conditional requirements (e.g. during pregnancy or infancy) – they are essential at certain times only
Phenylketonuria (PKU)
genetic condition that results in the impaired metabolism of the amino acid phenylalanine
It is an autosomal recessive disease caused by a mutation to the gene encoding the enzyme phenylalanine hydroxylase
Phenylalanine hydroxylase (PAH) normally converts excess phenylalanine within the body into tyrosine
In people with PKU, the excess phenylalanine is instead converted into phenylpyruvate (also known as phenylketone)
This results in a toxic build up of phenylketone in the blood and urine (hence phenylketonuria)
Untreated PKU can lead to brain damage and mental development issues, as well as other serious medical problems
PKU diagnosis & treatment
Infants with PKU are normal at birth because the mother is able to break down phenylalanine during pregnancy
Diagnosis of PKU is made by a simple blood test for elevated phenylalanine levels shortly after birth
PKU is treated by enforcing a strict diet that restricts the intake of phenylalanine to prevent its build up within the body
This low-protein diet should include certain types of fruits, grains, vegetables and special formula milk
This diet should be supplemented with a medical formula that contains precise quantities of essential amino acids
Patients who are diagnosed early and maintain this strict diet can have a normal life span without damaging symptoms
Lipids
Humans can synthesise most fatty acids from carbohydrates, but two (cis)-polyunsaturated fatty acids are considered essential
Alpha-linolenic acid (an omega-3 fatty acid) and linoleic acid (an omega-6 fatty acid) cannot be synthesised by the body
This is because humans lack the enzyme required to introduce double bonds at the required position of the carbon chain
Essential fatty acids are modified by the body to make important lipid-based compounds (such as signalling molecules)
There is evidence to suggest dietary deficiencies of these fatty acids may be linked to impaired brain development (e.g. depression) and altered maintenance of cardiac tissue (e.g. abnormal heart function) – although this evidence is contested
LDLs & HDLs
Low density lipoproteins (LDLs) carry cholesterol from the liver to the body (hence raise blood cholesterol levels)
High density lipoproteins (HDLs) carry excess cholesterol back to the liver for disposal (hence lower blood cholesterol levels)