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. 1998 Dec;64(12):4767–4773. doi: 10.1128/aem.64.12.4767-4773.1998

TABLE 3.

Toxicity thresholds of selected toxins and chemicals for vitality parameters of boar spermatozoa

Compound EC50 (ng ml−1) that resulted ina:
Swelling of mito-chondria Depletion of ATP Loss of motility Damage to plasma membrane
Purified toxin from indoor S. griseus strainsb
 8/ppi <500 >10,000 1 >1,000
 2/ppi <500 >10,000 3.2 >1,000
 10/ppi >10,000 2 >1,000
 1/k >10,000 2.9 >1,000
Cereulide <400 >1,000 0.5 >1,000
Valinomycin <400 >12,500 2 >1,000
Calcimycin A 23187 >2,000 125 32
Gramicidin (mixture of gramicidins A, B, C, and D) <3
Ionomycin >1,000 10,000 1,000
Polymyxin B sulfate >50,000 >50,000 >50,000
Surfactin >5,000 5,000–10,000 5,000
Enniatin >5,000 NDc 300
Nodularin ND >40,000 >40,000
Anatoxin A ND >40,000 >40,000
N,N-Dihexylcarbodi-imide 1,000 10,000 >100, <1,000
2,4-Dinitrophenol >10,000 >10,000 <10,000
a

Expressed as the endpoint dilution that resulted in a >50% change in the vitality parameter for extended boar semen compared to that of spermatozoa exposed to diluent only. Nodularin, anatoxin A, N,N-dihexylcarbodiimide, and 2,4-dinitrophenol were diluted in DMSO, and the other chemicals were diluted in methanol. Cereulide and valinomycin were diluted in parallel in methanol and in DMSO, but no difference in the endpoint dilutions was observed. 

b

The toxic agent was purified from methanol extracts of S. griseus cultures, and the amounts of toxic agent were determined by reverse-phase HPLC by using commercial valinomycin as the standard. 

c

ND, not determined.