So says Leviticus 17:11. Everyone knows that we must have enough blood flowing around our body or else our bodily functions deteriorate and we die. Yet for a long time the exact function of blood was little understood. In what ways has modern science shown Leviticus 17:11 to be true?
Blood is fundamental to the function of every cell of every component in our bodies. Cells need food to survive, grow, repair themselves and to fulfill their specific functions, and, to reproduce. Cellular food is transported in blood to provide energy for all the cells’ needs. As humans are multicellular organisms, having separate specialized organs with highly sophisticated functions, transport and communication between these structures is essential.
Do the cells of the body tell the blood how it should work? No. Does the blood carry around everything possible just in case? No. The cells and the blood work together to provide optimum conditions for correct functioning of all the cells—with their different requirements—in all the tissues and organs of the whole body, including the cells of the blood itself.
Blood provides this coordinated environment by regulating acidity/alkalinity (pH), providing oxygen (and removing carbon dioxide and other waste products), and carrying essential vitamins and minerals. Also, blood has to be in the right places at the right times, at the right temperature and pressure, and it carries regulatory messages between organs via blood ‘messengers’ called hormones. All this is organized within very specific limits—straying outside these (through injury, disease, toxins, etc.) rapidly reduces functionality.
FLESH (as used in many English translations of Leviticus 17:11): Hebrew בשר basar, the tissues that make up the body, and (by extension) also the body, the living creature.
TISSUE: a collection of cells (not necessarily the same type) grouped for a specific function. E.g. connective tissue, muscle tissue. Blood itself is, technically speaking, also a tissue.
ORGAN: several types of tissue functionally grouped together, e.g. liver, lung.
Hormones, those important chemical messengers in the blood, are involved in self-regulating feedback systems. These systems stimulate hormone production in times of lack, and suppress it in times of plenty. For example, when we eat, the sugars in the intestine are digested and absorbed into the local bloodstream. This blood then passes through the pancreas and its higher sugar level stimulates production of the hormone insulin. As insulin is distributed in the bloodstream, it reduces the blood sugar to normal levels again by increasing the amount of sugar that all cells take in. In fact the brain relies almost entirely on sugar (specifically glucose) for its energy supply; hence this feedback system is absolutely critical for proper brain activity. If the blood glucose ever drops too much, we lose consciousness.
The body’s systems tend to be wisely over-engineered, so that one might predict that there is also a system to cope with low sugar levels, for example when we exercise and use sugar up. This system uses the hormone glucagon (also from the pancreas) and it works by releasing glucose into the blood from stores located mostly in the liver.
There are about fifteen organs classed as hormone-producing (endocrine) glands,1 and their products, carried by the blood, affect either every cell in general or specifically target certain cells. Widely known examples are the male and female hormones testosterone and estrogen, adrenaline (epinephrine in the US), the thyroid hormone thyroxine, and many more.
The red colour of blood reflects the colour of the hemoglobin inside the red blood cells. This is because the hemoglobin contains iron. The ‘heme’ of the hemoglobin molecule in vertebrates (creatures with a backbone) is a porphyrin ring which surrounds ferrous iron atoms. It is the spatial relationship between heme, iron and globin which makes it possible to bind oxygen molecules reversibly—one to each iron—and which makes the system so efficient.
For example, thyroxine regulates the speed of metabolism in every cell, and having the correct amount (within narrow limits) allows normal cellular activity. Too much and we become ‘hyper’, too little and we are slow and lethargic.
Another example is gastrin. The target organ for gastrin is that part of the inner lining of the stomach which produces hydrochloric acid for digestion. Food in the last part of the stomach stimulates the production of gastrin, which is carried back by the blood to stimulate acid production. This is a positive feedback mechanism in which blood is the essential communicating link.
Blood also has a major role in body protection in that it is an integral part of the immune or infection-fighting system, involving antibodies and white blood cells. It also possesses a highly complex mechanism to prevent its own loss from the body (clotting) and to prevent clotting inside the body (thrombosis). The capacity to quickly initiate clotting outside and to limit—even reverse—clotting on the inside is provided by ‘cascades’—cumulative processes in which each step of the process is dependent on the one before it (see box). The cascades are of such complexity that new factors, cofactors and regulators are being constantly added to our body of knowledge. It is now known that there are more than a hundred factors or steps that make up the clotting cascade.2 Such details add to our appreciation of how finely balanced, effective and versatile the system is. But a greater marvel is that such a system, which is there in anticipation of blood loss, internal injury or disease, should be there at all.
Red blood cells (RBCs or erythrocytes) form the majority of the cells in the blood—and a quarter of all cells in the human body. They are unique among all others—in mammals, they have no nucleus and none of the usual energy-producing structures in the cell outside the nucleus. This is a design feature of mammals (creatures which, like us, suckle their young). Normally, a cellular nucleus carries the DNA which instructs the cell on how to perform its functions, including repair and reproduction, at the appropriate times. RBCs cannot do this because instead they are especially designed to carry oxygen, and in humans, having a nucleus would hinder this essential function. So the nucleus is lost after formation, leaving them with their characteristic biconcave shape.
There are about 4–6 million red blood cells (RBCs) in every cubic millimetre of blood; 20–30 trillion of them in each person.
Every day about 1% of these are changed. New RBCs take about 7 days to form in the bone marrow, and are produced at the staggering rate of about 2 to 3 million every second.
Each RBC lasts about 120 days before its components are recycled to form new RBCs.
During its 4-month lifetime, each red cell travels some 500 km (300 miles) around the body, passing through the heart about 14,000 times per day.
Most of our blood vessels are the microscopic capillaries. If the blood vessels in one person were laid end to end, they would be about 150,000 km (100,000 miles) in length—enough to circle the earth at the equator about four times!
*All figures are for a healthy adult
Two reasons have been suggested for this. First, the relative size of RBCs (6–8 µm diameter and just 2 µm thick)3 and capillaries (tiny blood vessels) is such that red blood cells often have to deform in order to squeeze through. A nucleus (about 6 µm on average4) could prevent passage of the cell and make it get stuck, blocking the circulation.
Second, the shape and deformability of the red blood cell is optimized for the carrying and delivery of oxygen, and it maximizes the amount of hemoglobin that can be packed into the cell. Nevertheless birds, which have a very high oxygen requirement, do fine with nucleated RBCs, so there are other design features in birds that compensate for this.5
The system of the red blood cells giving oxygen to the cells of the tissues is reversed when the red blood cell reaches the lungs, where it gives up its carbon dioxide (though this is mostly carried by plasma6) and takes on a new load of oxygen. At rest, all the blood (5 litres in an adult) completes a circuit within a minute (spending 1 to 3 seconds in the capillaries). With exercise, circulation is as quick as every 10 seconds.7 Having a molecule such as hemoglobin which can handle oxygen so quickly and reversibly, when required, is amazing.
So is the life of the flesh in the blood? Although not confirmed by science until modern times, this statement from Leviticus 17:11 has always been true. Blood actively maintains life by providing a vital function for all cells, tissues and organs, and thus the life of the whole body. The more we find out about the astounding functional design and complexity of blood, the more marvellous it becomes to us, and the more honour and praise is due its Creator.
The function of the blood clotting system is to prevent the escape of blood from a damaged vessel. To do this, the blood has a special and very complex repair procedure in place. Once initiated by a cut, the first component in the process is activated, which in turn activates the next component, and so on, in a series of cumulative, mutually-dependent steps. This physiological chain of production, or cascade, results in the formation of a solid obstruction (a clot) in order to seal over the damage.
Some of the main components of the clotting cascade are the proteins fibrinogen, prothrombin, Stuart (anti-hemophilic) factor and proaccelerin. None of these are used for any other purpose in the blood. The system is very finely tuned to result in a repair process that achieves just the repair needed at just the right place and time to stop bleeding and begin the process of healing. Importantly, the process is also self-limiting to ensure that coagulation (clotting) of the entire blood supply does not occur.
The Intelligent Design advocate Michael Behe, in his book Darwin’s Black Box, has noted that the clotting cascade is an example of irreducible complexity. The removal or degradation of just one, any one, of the components or steps would cause the cascade to fail. Obviously this would have dire consequences for the organism. It is exceedingly difficult to see how the clotting cascade could have evolved, as any postulated simplified or ‘primitive’ version of the process would result in failure.1