Authors

  • A. R. Ergashov
    Bukhara State Medical Institute, Bukhara, Uzbekistan

DOI:

https://doi.org/10.37547/ijmscr/Volume03Issue05-13

Keywords:

Aluminum Aluminum salts Aluminum oxide.

Abstract

Aluminum is ubiquitous; the third most common element of the earth's crust. It is naturally released to the environment from the weathering of rocks and volcanic activity. Human activities such as mining also result in the release of aluminum to the environment. Aluminum levels in environmental media vary widely depending upon the location and sampling site. In general, background levels of aluminum in the atmosphere are low, typically ranging from about 0.005 to 0.18 μg/m3. Much higher levels are routinely observed in urban and industrial locations. Aluminum levels in surface water is usually very low (<0.1 mg/L); however, in acidic waters or water high in humic or fulvic acid content, the concentration of soluble aluminum increases due to the increased solubility of aluminum oxide and aluminum salts. Its concentration in soils varies widely, ranging from about 7 to over 100 g/kg.


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ABSTRACT

Aluminum is ubiquitous; the third most common element of the earth's crust. It is naturally released to the

environment from the weathering of rocks and volcanic activity. Human activities such as mining also result in the

release of aluminum to the environment. Aluminum levels in environmental media vary widely depending upon the

location and sampling site. In general, background levels of aluminum in the atmosphere are low, typically ranging

from about 0.005 to 0.18 μg/m3. Much higher levels are routinely

observed in urban and industrial locations. Aluminum

levels in surface water is usually very low (<0.1 mg/L); however, in acidic waters or water high in humic or fulvic acid

content, the concentration of soluble aluminum increases due to the increased solubility of aluminum oxide and

aluminum salts. Its concentration in soils varies widely, ranging from about 7 to over 100 g/kg.

KEYWORDS

Aluminum, Aluminum salts, Aluminum oxide.

INTRODUCTION

In the environment, aluminum exists in only one

oxidation state (+3), and does not undergo

oxidationreduction reactions. It can react with other

matter in the environment to form various complexes.

The fate and transport of aluminum is largely

controlled by environmental factors such as pH,

salinity, and the presence of various species with which

it may form complexes. In general, the solubility and

mobility of aluminum in soil is greatest when the soil is

rich in organic matter capable of forming aluminum-

Research Article

THE GENERAL EFFECT OF ALUMINUM ON THE BODY

Submission Date:

May 21, 2023,

Accepted Date:

May 26, 2023,

Published Date:

May 31, 2023

Crossref doi:

https://doi.org/10.37547/ijmscr/Volume03Issue05-13


A. R. Ergashov

Bukhara State Medical Institute, Bukhara, Uzbekistan

Journal

Website:

https://theusajournals.
com/index.php/ijmscr

Copyright:

Original

content from this work
may be used under the
terms of the creative
commons

attributes

4.0 licence.


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organic complexes and when the pH is low, such as in

areas prone to acid rain or in acidic mine tailings. The

general population is primarily exposed to aluminum

through the consumption of food items, although

minor exposures may occur through ingestion of

aluminum in drinking water and inhalation of ambient

air. Aluminum found in over-the-counter medicinals,

such as antacids and buffered aspirin, is used as a food

additive, and is found in a number of topically applied

consumer products such as antiperspirants, and first

aid antibiotic and antiseptics, diaper rash and prickly

heat, insect sting and bite, sunscreen and suntan, and

dry skin products. The concentration of aluminum in

foods and beverages varies widely, depending upon

the food product, the type of processing used, and the

geographical areas in which food crops are grown.

Based on th

e FDA’s 1993 Total Diet Study dietary

exposure model and the 1987

1988 U.S. Department

of Agriculture (USDA) Nationwide Food Consumption

Survey, the authors estimated daily aluminum intakes

of 0.10 mg Al/kg/day for 6

11-month-old infants; 0.30

0.35 mg Al/kg/day for 2

6-year-old children; 0.11 mg

Al/kg/day for 10-yearold children; 0.15

0.18 mg

Al/kg/day for 14

16-year-old males and females; and

0.10

0.12 mg Al/kg/day for adult (25

30- and 70+-year-

old) males and females. Users of aluminum containing

medications who are healthy (i.e., have normal renal

function) can ingest much larger amounts of aluminum

than in the diet, possibly as high as 12

71 mg Al/kg/day

from antacid/anti-ulcer products and 2

10 mg Al/kg/day

from buffered analgesics when taken at recommended

dosages [1,2].

Gastrointestinal absorption of aluminum is low,

generally in the range of 0.1

0.4% in humans, although

absorption of particularly bioavailable forms such as

aluminum citrate may be on the order of 0.5

5%.

Although large bolus doses of as much as half a gram

of aluminum as aluminum hydroxide throughout the

day can be ingested during antacid therapy, absorption

of aluminum hydroxide is usually ≤0.01% of the intake

amount. Bioavailability of aluminum varies depending

mainly on the chemical form of the ingested compound

(i.e., type of anion) and the concurrent exposure to

dietary chelators such as citric acid, ascorbic acid, or

lactic acid. The total div burden of aluminum in

healthy human subjects is approximately 30

50 mg.

Normal levels of aluminum in serum are approximately

1

–3 μg/L. Of the total div burden of aluminum, about

one-half is in the skeleton, and about one-fourth is in

the lungs.

There are numerous studies that have examined

aluminum’s potential to induce toxic effects in huma

ns

exposed via inhalation, oral, or dermal exposure. Most

of these findings are supported by a large number of

studies in laboratory animals. Occupational exposure

studies and animal studies suggest that the lungs and

nervous system may be the most sensitive targets of

toxicity following inhalation exposure.


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Respiratory effects, in particular impaired lung

function and fibrosis, have been observed in workers

exposed to aluminum dust or fumes; however, this has

not been consistently observed across studies and it is

possible that co-exposure to other compounds

contributed to observed effects. Respiratory effects

(granulomatous lesions) have also been observed in

rats, hamsters, and guinea pigs. There is concern that

these effects are due to dust overload rather than a

direct effect of aluminum in lung tissue. Occupational

studies in workers exposed to aluminum dust in the

form of McIntyre powder, aluminum dust and fumes in

potrooms, and aluminum fumes during welding

provide suggestive evidence that there may be a

relationship between chronic aluminum exposure and

subclinical neurological effects such as impairment on

neurobehavioral tests for psychomotor and cognitive

performance and an increased incidence of subjective

neurological symptoms. With the exception of some

isolated cases, inhalation exposure has not been

associated with overt symptoms of neurotoxicity. A

common limitation of these occupational exposure

studies is that aluminum exposure has not been well

characterized. The available animal inhalation studies

are inadequate for assessing the potential for

aluminum-induced neurotoxicity because the only

neurological end points examined were brain weight

and histology of the brain; no function tests were

performed.

There is limited information on aluminum toxicity

following dermal exposure. Application of aluminum

compounds to the skin, such as aluminum chloride in

ethanol or alum, may cause rashes in some people. Skin

damage has been observed in mice, rabbits, and pigs

exposed to aluminum chloride or aluminum nitrate,

but not following exposure to aluminum sulfate,

aluminum hydroxide, aluminum acetate, or aluminum

chlorhydrate. There is a fair amount of human data on

the toxicity of aluminum following oral exposure.

However, the preponderance of human studies are in

patients with reduced renal function who accumulated

aluminum as a result of long-term intravenous

hemodialysis therapy with aluminum-contaminated

dialysis fluid and, in many cases, concurrent

administration of high oral doses of aluminum to

regulate phosphate levels (i.e., reduce uptake of

phosphate by binding it in the gut) and have limited

usefulness in predicting toxicity in the general

population because the very large aluminum exposure

levels and impaired renal function results in aluminum

accumulation. Dialysis encephalopathy syndrome (also

referred to as dialysis dementia) can result from this

accumulation of aluminum in the brain. Dialysis

encephalopathy is a degenerative neurological

syndrome, characterized by the gradual loss of motor,

speech, and cognitive functions. Another neurological

effect that has been proposed to be associated with

aluminum exposure is Alzheimer’s disease. Although a

possible association was proposed over 40 years ago,


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this association is still highly controversial and there is

little consensus regarding current evidence. A number

of studies have found weak associations between

living in areas with elevated aluminum levels in drinking

water and an increased risk (or prevalence) of

Alzheimer’s disease; other studi

es have not found

significant associations. In contrast, no significant

associations have been found between tea

consumption or antacid use and the risk of Alzheimer’s

disease; although the levels of aluminum in tea and

antacids are very high compared to drinking water,

aluminum from these sources is poorly absorbed [3,4].

The available data do not suggest that aluminum is a

causative agent of Alzheimer’s disease; however, it is

possible that it may play a role in the disease

development. Aluminum is found in several ingested

over-the-counter products such as antacids and

buffered aspirin; clinical studies on health effects of

aluminum medicinals in people with normal renal

function have been identified. These aluminum-

containing products are assumed to be safe in healthy

individuals at recommended doses based on historical

use. The assumed safety of aluminum is also partly due

to the generally regarded as safe (GRAS) status of

aluminum-containing food additives. However, there is

some indication that adverse effects can result from

long-term use of aluminum-containing medications in

some healthy individuals. There are a number of case

reports of skeletal changes (e.g., osteomalacia) in

adults and children with normal kidney function due to

long-term antacid use for the treatment of

gastrointestinal disorders. These skeletal effects are

secondary to hypophosphatemia and phosphate

depletion caused by aluminum impairing phosphorus

absorption by binding with dietary phosphorus [5,6].

There is a rather extensive database on the oral toxicity

of aluminum in animals. These studies clearly identify

the nervous system as the most sensitive target of

aluminum toxicity and most of the animal studies have

focused on neurotoxicity and neurodevelopmental

toxicity. Other adverse effects that have been

observed in animals orally exposed to aluminum

include impaired erythropoiesis in rats exposed to 230

mg Al/kg/day and higher, erythrocyte damage (as

evidenced by decreases in hemoglobin, hematocrit,

and erythrocyte osmotic fragility, and altered

erythrocyte morphology) in rats exposed to 230 mg

Al/kg/day and higher, increased susceptibility to

infection in mouse dams exposed to 155 mg Al/kg/day,

delays in pup maturation following exposure of rats to

53 mg Al/kg/day, and decreases in pup div weight

gain in rats and mice exposed to 103 mg Al/kg/day and

higher. Neurodegenerative changes in the brain,

manifested as intraneuronal hyperphosphorylated

neurofilamentous aggregates, is a characteristic

response to aluminum in certain species and non-

natural exposure situations generally involving direct

application to brain tissue, particularly intracerebral


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and intracisternal administration and in vitro

incubation in rabbits, cats, ferrets, and nonhuman

primates. Oral studies in rats and mice have not found

significant histopathological changes in the brain

under typical exposure conditions; however, altered

myelination was found in the spinal cord of mouse

pups exposed to 330 mg Al/kg/day on gestation day 1

through postnatal day 35. Overt signs of neurotoxicity

are rarely reported at the doses tested in the available

animal studies ( ≤330mg Al/kg/day for bioavailable

aluminum compounds); rather, exposure to these

doses is associated with subtle neurological effects

detected with neurobehavioral performance tests.

Significant alterations in motor function, sensory

function, and cognitive function have been detected

following exposure to adult or weanling rats and mice

or following gestation and/or lactation exposure of

rats and mice to aluminum lactate, aluminum nitrate,

and aluminum chloride. The most consistently affected

performance tests were forelimb and/or hind limb grip

strength, spontaneous motor activity, thermal

sensitivity, and startle responsiveness. Significant

impairments in cognitive function have been observed

in some studies, although this has not been found in

other studies even at higher doses. Adverse

neurological effects have been observed in rats and

mice at doses of 100

200 mg Al/kg/day and

neurodevelopmental effects have been observed in

rats and mice at doses of 103

330 mg Al/kg/day

[1,2,7,8].

A number of human studies have examined the

occurrence of cancer among aluminum industry

workers and found a higher-than-expected cancer

mortality rate, but this is probably due to the other

potent carcinogens to which they are exposed, such as

polycyclic aromatic hydrocarbons (PAHs) and tobacco

smoke. Available cancer studies in animals have not

found biologically relevant increases in malignant

tumors. The International Agency for Research on

Cancer (IARC) concluded that aluminum production

was carcinogenic to humans and that pitch volatiles

have

fairly

consistently

been

suggested

in

epidemiological studies as being possible causative

agents. The Department of Health and Human Services

and EPA have not evaluated the human carcinogenic

potential of aluminum.

REFERENCES

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Krewski, D., Yokel, R. A., Nieboer, E., Borchelt,

D., Cohen, J., Harry, J., Kacew, S., Lindsay, J.,

Mahfouz, A. M., & Rondeau, V. (2007). Human

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aluminium oxide, and aluminium hydroxide.

Journal of toxicology and environmental

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Poole, R. L., Pieroni, K. P., Gaskari, S., Dixon, T.,

& Kerner, J. A. (2012). Aluminum exposure in

neonatal patients using the least contaminated


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R. Ergashov. (2023). RESULTS OF EARLY

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PATIENTSINJURY TO THE THORACO-LUMBAR

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Эргашов А. Р. (2022). ОЦЕНКА

ОСТРОЙ ТРАВМЫ ГРУДОПОЯСНИЧНОГО

ОТДЕЛА ПОЗВОНОЧНИКА ПО КЛИНИКО

-

НЕВРОЛОГИЧЕСКИМ НАРУШЕНИЯМ ДО И

ПОСЛЕ

СТАБИЛИЗИРУЮЩИМИ

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Dec -2022 ISSN: 2181-2608 www.sciencebox.uz

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SCIENCES, 2(3), 3-5.

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Obidovna, D. Z., & Sulaymonovich, D. S. (2023).

Forming a Healthy Lifestyle for Students on the

Example of the Volleyball Section in

Universities.

EUROPEAN

JOURNAL

OF

INNOVATION IN NONFORMAL EDUCATION,

3(3), 22-25

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Krewski, D., Yokel, R. A., Nieboer, E., Borchelt, D., Cohen, J., Harry, J., Kacew, S., Lindsay, J., Mahfouz, A. M., & Rondeau, V. (2007). Human health risk assessment for aluminium, aluminium oxide, and aluminium hydroxide. Journal of toxicology and environmental health. Part B, Critical reviews, 10 Suppl 1 (Suppl 1), 1–269. https://doi.org/10.1080/10937400701597766

Poole, R. L., Pieroni, K. P., Gaskari, S., Dixon, T., & Kerner, J. A. (2012). Aluminum exposure in neonatal patients using the least contaminated parenteral nutrition solution products. Nutrients, 4(11), 1566–1574. https://doi.org/10.3390/nu4111566

R., E. (2022). Principles of Diagnosis and Surgical Treatment of Injuries of the Thoraco-Lumbar Spine. INTERNATIONAL JOURNAL OF HEALTH SYSTEMS AND MEDICAL SCIENCES, 1(4), 69–73. Retrieved from https://inter-publishing.com/index.php/IJHSMS/article/view/149

Ergashov , A. R. (2022). Modern Clinical Analysis of Injuries of the Thoracolumbar Spine. INTERNATIONAL JOURNAL OF HEALTH SYSTEMS AND MEDICAL SCIENCES, 1(4), 59–63. Retrieved from https://inter-publishing.com/index.php/IJHSMS/article/view/146

Эргашов , А. Р. (2022). Отдаленные Результаты Хирургического Леченияпри Острой Травме Грудопоясничного Отдела Позвоночника. Central Asian Journal of Medical and Natural Science, 3(2), 256-260. https://doi.org/10.17605/OSF.IO/7A4EG

Эргашов, А. Р. (2021). Характеристика Острой Травмы Грудопоясничного Отдела Позвоночника. Central Asian Journal of Medical and Natural Science, 150-153. https://doi.org/10.47494/cajmns.vi0.367

R. Ergashov. (2023). RESULTS OF EARLY POSTOPERATIVE TREATMENT OF PATIENTSINJURY TO THE THORACO-LUMBAR SPINE. Open Access Repository, 4(3), 1171–1182. https://doi.org/10.17605/OSF.IO/MV4NB

Эргашов А. Р. (2022). ОЦЕНКА ОСТРОЙ ТРАВМЫ ГРУДОПОЯСНИЧНОГО ОТДЕЛА ПОЗВОНОЧНИКА ПО КЛИНИКО-НЕВРОЛОГИЧЕСКИМ НАРУШЕНИЯМ ДО И ПОСЛЕ СТАБИЛИЗИРУЮЩИМИ ОПЕРАЦИЯМИ. Journal of Advanced Research and Stability Volume: 02 Issue: 12 | Dec -2022 ISSN: 2181-2608 www.sciencebox.uz

Obidovna, D. Z., & Sulaimonovich, D. S. (2023). Influence of the Mode of Work and Recreation of the Student's Health. INTERNATIONAL JOURNAL OF HEALTH SYSTEMS AND MEDICAL SCIENCES, 2(3), 3-5.

Obidovna, D. Z., & Sulaymonovich, D. S. (2023). Forming a Healthy Lifestyle for Students on the Example of the Volleyball Section in Universities. EUROPEAN JOURNAL OF INNOVATION IN NONFORMAL EDUCATION, 3(3), 22-25