Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2021 Mar 24;11(4):923.
doi: 10.3390/ani11040923.

Roles of Nitrocompounds in Inhibition of Foodborne Bacteria, Parasites, and Methane Production in Economic Animals

Affiliations
Review

Roles of Nitrocompounds in Inhibition of Foodborne Bacteria, Parasites, and Methane Production in Economic Animals

Po-Yun Teng et al. Animals (Basel). .

Abstract

Nitrocompounds are derivatives of hydrocarbons, alcohols, fatty acids, and esters, consisting one or more nitro functional groups. Either natural sources of nitrocompounds or synthetic chemicals have been applied in animal diets to investigate their effects on economic animals, since conjugates of 3-nitropropanol and 3-nitropropionic acid were isolated from Astragalus oblongifolius. In this review, emphasis will be placed on nitrocompounds' antimicrobial activity, toxicity, metabolisms and mechanisms of actions. Nitrocompounds can be metabolized by ruminal microbials, such as Denitrobacterium detoxificans, or alcohol dehydrogenase in the liver. Moreover, it has been found that nitrocompounds are capable of inhibiting pathogens, parasites, methane and ammonia production; however, overdose of nitrocompounds could cause methemoglobinemia or interfere with energy production in mitochondria by inhibiting succinate dehydrogenase.

Keywords: nitrocompounds; nitroethanol; nitropropanol.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Metabolism of natural sources of nitrocompounds in ruminants and non-ruminants. (A) Glucose esters of 3-nitropropionic acid; (B) glycoside of 3-nitro-propanol (3-nitro-1-propyl-beta-D-glucopyranoside); (C) 3-nitropropionic acid; (D) 3-nitropropanol; (E) 3-aminopropionic acid (β-alanine); (F) nitrite; (G) 3-aminopropanol.
Figure 2
Figure 2
Mechanisms of actions of nitrite poisoning caused by nitrocompounds administration. Once nitrocompounds are metabolized to nitrite in the gastrointestinal tracts in animals, nitrite will interact with both oxyhemoglobin and deoxyhemoglobin, leading to failure of oxygen transportation. Nitrite could further initiate an autocatalytic propagation that keep oxidizing oxyhemoglobin to methemoglobin and end up with the formation of nitrosyl hemoglobin.
Figure 3
Figure 3
Inhibition of succinate dehydrogenase in electron transport chain by 3-nitropropionic acid (3NPA). 3NPA has a similar chemical structure as succinic acids which make it possible to attach on succinate dehydrogenase and irreversibly inactive the enzyme, causing failure of electron transportation in mitochondria.
Figure 4
Figure 4
Possible mechanisms of actions of nitrocompounds withhold methanogenesis in ruminants. Nitrocompounds might directly inhibit methanogens [pathway 1] or suppress dehydrogenase which is an enzyme metabolizing formate to methane [pathway 2]. Metabolism of Nitrocompounds by D. detoxificans consumes reductant in the rumen, such as hydrogen and formate. Nitrocompounds might compete these reductants with carbon dioxides, indirectly reducing methane production. [pathway 3] Reductant competition is a possible mechanism of action of nitrocompounds, but it might not play the main role on inhibition of methanogenesis in ruminants.

Similar articles

Cited by

References

    1. Zhang Z.-W., Cao Z.-J., Wang Y.-L., Wang Y.-J., Yang H.-J., Li S.-L. Nitrocompounds as potential methanogenic inhibitors in ruminant animals: A review. Anim. Feed Sci. Tech. 2018;236:107–114. doi: 10.1016/j.anifeedsci.2017.12.010. - DOI
    1. Shvekhgeimer M.-G.A. Aliphatic nitro alcohols. Synthesis, chemical transformations and applications. Russ. Chem. Rev. 1998;67:35–68. doi: 10.1070/RC1998v067n01ABEH000285. - DOI
    1. Gustine D.L. Aliphatic Nitro Compounds in Crownvetch: A Review. Crop. Sci. 1979;19:197–203. doi: 10.2135/cropsci1979.0011183X001900020007x. - DOI
    1. Anderson R.C., Majak W., Rassmussen M.A., Callaway T.R., Beier R.C., Nisbet D.J., Allison M.J. Toxicity and metabolism of the conjugates of 3-nitropropanol and 3-nitropropionic acid in forages poisonous to livestock. J. Agric. Food Chem. 2005;53:2344–2350. doi: 10.1021/jf040392j. - DOI - PubMed
    1. Stermitz F.R., Norris F.A., Williams M.C. Miserotoxin, new naturally occurring nitro compound. J. Am. Chem. Soc. 1969;91:4599–4600. doi: 10.1021/ja01044a078. - DOI

LinkOut - more resources