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Classification of Agni based on its location
Depending upon the stage of metabolism where a specific Agni is functionally active, Agni has been classified into three sub-classes: 'Jaṭharāgni', 'Bhūtāgni' and 'Dhātvagni'.
While Jaṭharāgni acts acts on the food in the digestive tract and converts it into absorbable form, the Bhūtāgni acts after the digested material has been absorbed.
Bhūtāgni is of 5 types. Each of these 5 acts on the 5 primordial constituents of the absorbed food: Earth, Water, Fire, Air, and Space. These 5 Bhutagnis transform the substrates into such form that can be assimilated at tissue level.
The third class of Agni, the Dhātvagni, acts at the level of tissue metabolism and is helpful in the tissue nourishment tissue metabolism. This is of 7 types based on the kind of tissue that it helps nourishing.
Classification of Agni based on its strength
Samāgni ensures complete digestion of the food ingested at the proper time without any irregularity. Its activity is neither too intense nor too weak. It is just appropriate and therefore, is ideal too. Ths results when all Doshas, Vata-Pitta-Kapha are in a state of equilibrium.
Vişamāgni represents an unpredictable state of Agni, which is due to the dominance of Vayu. It sometimes quickly digests the food and at other times it does so very slowly, representing unpredictability.
Tīkşņāgni results because of the dominance of Pitta which is intense, and hence, it easily digests even a very heavy meal, in a very short span of time.
Mandāgni is opposite to the Tīkşņāgni: it is subdued in its activity. This Agni is unable to digest and metabolize even a small quantity of food. This state of Agni is a result of the dominance of Kapha.
- Mishra, Lakshmi C. (2003). Scientific Basis for Ayurvedic Therapies. CRC Press. pp. 307–322. ISBN 0-8493-1366-X.
- Singh, Aparna; Singh, Girish; Patwardhan, Kishor; Gehlot, Sangeeta (2017). "Development, Validation, and Verification of a Self-Assessment Tool to Estimate Agnibala (Digestive Strength)". J Evid Based Complementary Altern Med. 22 (1): 134–140. doi:10.1177/2156587216656117. PMID 27381899.