| Review Article | 
INTRODUCTION
Workers are commonly simultaneously exposed to multiple chemical agents. Simultaneous exposure to lead and 
cadmium is highly probable in mining and smelting operations. Compounds of both metals are present in paints, solder, 
storage batteries, ceramics, glazing material. It is important to determine if the effects of specific compounds on 
biological functions are modified by the concomitant exposure to other compounds. Lead and cadmium exert toxic 
effects on hematopoietic, cardiovascular, reproductive and nervous systems in addition to causing lesions in the 
liver and kidneys.
     
     The central question involves the nature of the possible interactions between 
these contaminants and their consequences on the toxicity of a mixture. Is the toxicity simply the sum of the toxic 
effects of the individual substances at the same level of exposure? Or do the substances in the mixture interact 
supra-additively, thus producing an effect greater than the sum of the effects of the individual substances? Or does 
the interaction lead to a reduction in the effects of each of the components in the mixture, producing an antagonistic 
situation (infra-additivity)?
     
     Regulations and common industrial practices address the question of interactions 
by hypothesizing, by default, that toxic effects on common target organs are additive. The Quebec “Regulation Respecting 
Occupational Health end Safety” (RROHS) similarly to the ACGIH® approach  prescribes that “where two or 
more substances are present in the work location and where they have similar effects on the same organs of the human 
body, the effects of these substances are considered to be additive, unless it is established otherwise”. In some 
cases, this hypothesis may lead to an underestimation or an overestimation of the actual risk.
     
     The aim of this study was the evaluation of toxicological studies allowing the 
identification of possible additive or other interactive effects in mixtures of cadmium and lead in work environments.
METHODOLOGY
Information was taken from primary references available in databases up to July 2007. We utilized the databases 
MixTox, POLTOX and TOXLINE. We also consulted the toxicological on line database developed and maintained by the Quebec 
Occupational Health and Safety Commission CSST.
     
     The interactions were evaluated only for realistic exposure concentrations in 
workplaces based on the permissible exposure limit values. In Quebec, the time-weighed average exposure value (TWAEV- the 
average concentration of a given chemical to which workers can be exposed for normal 8-hour workdays, 5 days a week) 
is 0.025 and 0.05 mg/m3 for cadmium and lead, respectively, including oxides and salts. These 
concentrations correspond to permissible daily doses of 0.0036 and 0.0071 mg/kg/d, respectively, using default 
worker’s lung ventilation of 10 m3/workshift and body weight of 70 kg.
     
     In humans, the toxicological data were evaluated only for exposure 
concentrations/doses up to 5 times the TWAEV. This factor was chosen because, according to the RROHS, “none of the 
excursions in exposure levels may exceed 5 times the time-weighted average exposure value during any length of time 
whatsoever”. Animal data were used when no human data were available. In this case, the data were evaluated only for 
exposure concentrations up to 100 times the TWAEV [factor of 10 for extrapolation of the LOAEL (lowest observed 
adverse effect level) towards the NOAEL (no observed adverse effect level) and 10 for the differences between species]. 
In some cases, the ACGIH TLV® Committee uses these uncertainty factors to establish the “Threshold Limit Value” 
(TLV®) from animal data, when there are no satisfactory human data available, and Quebec regulation is largely 
based on ACGIH recommendations.
     
     Doses/concentrations of lead or cadmium reported in various studies were converted 
to daily doses in mg/kg body weight/d using EPA Documentation of Biological Values for Use in Risk Assessment and the 
ratio of administered dose to permissible limit dose was calculated.
RESULTS AND DISCUSSION
After screening exposure concentrations/doses, six studies were retained (Table 1). Chronically feeding rats with either cadmium or lead can induce a significant increase in systolic pressure. Perry et al. and Perry and Erlanger exposed female rats to 0.1, 1 and 5 ppm lead and/or cadmium in drinking water for up to 6 months. Administering both metals together usually doubled the increase of systolic pressure observed with either metal alone. In one experiment, the effect was supra-additive after 3 months of exposure to 1 ppm lead and cadmium producing an average increase of 43 mm Hg in systolic pressure. The average systolic pressures of 103, 115, 116 and 146 mm Hg were observed in controls and after exposure to lead, cadmium and the combination of both metals, respectively. These studies clearly indicate at least an additive effect for the mixture of lead and cadmium.
TABLE 1. Effects of combined exposure to cadmium and lead
| Compound | Reported | Calculated daily | Ratiob | Target organ/system | Effects | Type of interaction | References | ||||
| Cd | Pb | Cd | Pb | ||||||||
| Cadmium acetate | Lead chloride | 1 ppm Cd in drinking water | 1 ppm Pb in drinking water | 0.23 | 0.23 | 65 | 33 | Cardiovascular system | Hypertension | ND | (Perry et al., 1983) | 
| Cadmium acetate | Lead chloride | 0.1; 1; 5 ppm Cd in drinking water | 0.1; 1; 5 ppm Pb in drinking water | 0.023–1.15 | 0.023–1.15 | 7– | 3– | Cardiovascular system | Hypertension | ADD | (Perry and Erlanger, 1978) | 
| Cadmium acetate | Lead chloride | 0.1; 1 ppm Cd in drinking water | 0.1; 1 ppm Pb in drinking water | 0.023–0.23 | 0.023–0.23 | 7– | 7– | Cardiovascular system | Hypertension | ADD or SUPRA | (Perry et al., 1979) | 
| Cadmium chloride | Lead acetate | 0,025 mg Cd | 0,025 mg Pb | 0.083 | 0.083 | 23 | 12 | Testes, liver, adrenal, kidney, spleen | Weight changes | ND | (Der et al., 1976) | 
| Testes | Degeneration | ND | |||||||||
| Cadmium chloride | Lead acetate | 0.0132 mg Cd/m3 | 0.0024 mg Pb/m3 | – | – | 0.5 | 0.05 | Lung | Bronchiolar damage | ADD | (Fortoul et al., 2004) | 
| Cadmium acetate | Lead acetate | 0.045 mg Cd/kg/d | 0.03 mg Pb/kg/d | 0.045 | 0.03 | 13 | 5 | Endocrine system | Hormonal disturbances | ND | (Pillai et al., 2003) | 
     In another study from the same laboratory Perry et al. exposed female rats 
to 1 ppm cadmium or 1 ppm cadmium plus 1 ppm lead in drinking water for 20 months. Exposure to the 
combination of lead and cadmium initially produced higher systolic pressures than cadmium alone (117 
vs 109 mm Hg after 8 months), but this difference disappeared in middle age (124 
vs 125 mm Hg after 16 months) and was reversed in old age (125 vs 132 mm Hg after 
20 months). This trend reproduces prior observations that the initially significant effect of lead alone diminished 
with continued exposure and eventually became insignificant. This study does not allow to draw a conclusion on a possible 
interactive or additive effects as the authors did not expose the rats to lead only.
     
     Der et al. injected Sprague Dawley male rats daily with 0.050 and 
0.250 mg of lead (as lead acetate) or cadmium (as cadmium chloride) or with 0.025 mg of both lead and cadmium 
for 70 days. Lead acetate was administered intraperitoneally and cadmium chloride intramuscularly. No effects were 
found on weight of testes, liver, adrenals, kidney, spleen or prostate after combined exposure. In animals treated with 
lead and cadmium alone, no pathological or histological changes were noted in the testes, prostate, epididymis or seminal 
vesicle. Authors declared that “testes histology of a group with simultaneous administration of the two metals showed an 
absence of spermatogenesis in some seminiferous tubules and an increase in the size of seminiferous tubules with large 
vacuoles in the centre indicating that low levels of lead and cadmium administered together have more synergic damaging 
effect on testes than higher levels of lead or cadmium alone” without any clear demonstration of the effects on the rats 
treated with either metals alone. This study does not allow to conclude on a possible interactive or additive effects as 
the individual doses were different from combined doses.
     
     Fortoul et al. studied the effects of inhalation of lead and cadmium alone 
and in mixture on mouse bronchiolar ultrastructure. CD1 adult male mice inhaled nebulized 0.01 M lead acetate and 
0.006 M cadmium chloride alone or in combination for 1 h twice a week for 8 weeks. Average concentrations 
of Cd and Pb in the inhalation chamber were 27.1 and 6.6 µg/m3, respectively, during individual inhalation 
and only 13.2 and 2.4 µg/m3 during simultaneous inhalation. Morphological changes in the bronchiole were 
mainly observed in the mixture, with a decreased number of nonciliated bronchiolar cells and an increased number of bundles 
of dividing cells. Additive effect of Pb and Cd was suggested by the authors. However, combined exposure at a concentration 
that was lower than the individual exposures produces effect on bundles that was much higher than predicted if the effects 
were purely additive. It should therefore be considered that combined exposure to Pb and Cd leads to supraadditive effects 
on this parameter. So this study does not allow drawing a final conclusion on interactive or additive effects in bronchiolar 
epithelium as the individual doses were different from combined doses but it suggests minimally an additive effect.
     
     The effects of lead and cadmium on the hypothalamic-pituitary axis was studied in 
proestrous rats by Pillai et al.. Adult female rats were treated intraperitoneally with either lead acetate and 
cadmium acetate alone or in combination at a dose of 0.05 mg/kg daily for 15 days. Hypothalamic serotonin (5-HT), 
dopamine (DA) and norepinephrine (NE) and plasma and pituitary levels of luteinizing hormone (LH) and follicle stimulating 
hormone (FSH) were measured. 5-HT and NE levels decreased in individually and combined metal treated groups whereas DA 
levels were decreased only in Cd-exposed group. The pituitary levels of LH and FSH were decreased significantly in Cd and 
combined treatment groups. Lead exposure failed to cause any changes in serum LH and FSH levels, whereas Cd and combined 
treatments showed significant decrease in serum LH and FSH levels. According to the authors, the hormonal disturbances 
following combined treatment with lead and cadmium more often paralleled the effects of cadmium alone than the changes seen 
in lead alone. It is clear that the effects produced by the combined treatment with Cd and Pb on the hypothalamic-pituitary 
axis are not additive.
CONCLUSION
It is evident that combined exposure to lead and cadmium in mammalian biological systems alter effects produced by 
the individual metals. Cadmium and lead were suggested as a possible cause of human hypertension. However, unlike the 
cadmium effect, the lead effect seemed to decrease with time. Studies by Perry et al. and Perry and Erlanger on rats 
clearly indicate an additive effect for the mixture of lead and cadmium. The study of Der et al. on reproduction in male 
rats is not convincing. The study of Fortoul et al. suggests supraadditive effect in the bronchiolar epithelium. 
Finally, the study of Pillai et al. shows no interactive effects in the hypothalamic-pituitary axis.
     
     The applicability of these results to man remains to be proven but reported effects 
resulted from realistic doses of lead and cadmium in comparison to occupation doses. In conclusion, based on the studies 
of Perry et al., Perry and Erlanger and Fortoul et al., we recommend to consider at least an additive effect 
for the mixture of cadmium and lead.
ACKNOWLEDGEMENT
This study was supported by the Institut de recherche Robert-Sauvé en santé et en sécurité du travail (Quebec, Canada). We are grateful to Mrs. F. Gagnon for skilful technical assistance.
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