# The Torpid State: Recent Advances in Metabolic Adaptations and Protective Mechanisms†

**Authors:** Sylvain Giroud, Caroline Habold, Roberto F. Nespolo, Carlos Mejías, Jérémy Terrien, Samantha M. Logan, Robert H. Henning, Kenneth B. Storey

PMC · DOI: 10.3389/fphys.2020.623665 · Frontiers in Physiology · 2021-01-20

## TL;DR

This review explores how animals use torpor and hibernation to survive scarce resources by reducing metabolism and protecting organs.

## Contribution

The paper compares metabolic and protective mechanisms in torpor across different species, including tropical ones.

## Key findings

- Torpor enables significant metabolic suppression in various species, aiding survival during food scarcity.
- Hydrogen sulfide (H2S) plays a key role in protecting organs during torpor and recovery.
- Comparative analysis reveals unique adaptations in tropical and temperate heterotherms.

## Abstract

Torpor and hibernation are powerful strategies enabling animals to survive periods of low resource availability. The state of torpor results from an active and drastic reduction of an individual’s metabolic rate (MR) associated with a relatively pronounced decrease in body temperature. To date, several forms of torpor have been described in all three mammalian subclasses, i.e., monotremes, marsupials, and placentals, as well as in a few avian orders. This review highlights some of the characteristics, from the whole organism down to cellular and molecular aspects, associated with the torpor phenotype. The first part of this review focuses on the specific metabolic adaptations of torpor, as it is used by many species from temperate zones. This notably includes the endocrine changes involved in fat- and food-storing hibernating species, explaining biomedical implications of MR depression. We further compare adaptive mechanisms occurring in opportunistic vs. seasonal heterotherms, such as tropical and sub-tropical species. Such comparisons bring new insights into the metabolic origins of hibernation among tropical species, including resistance mechanisms to oxidative stress. The second section of this review emphasizes the mechanisms enabling heterotherms to protect their key organs against potential threats, such as reactive oxygen species, associated with the torpid state. We notably address the mechanisms of cellular rehabilitation and protection during torpor and hibernation, with an emphasis on the brain, a central organ requiring protection during torpor and recovery. Also, a special focus is given to the role of an ubiquitous and readily-diffusing molecule, hydrogen sulfide (H2S), in protecting against ischemia-reperfusion damage in various organs over the torpor-arousal cycle and during the torpid state. We conclude that (i) the flexibility of torpor use as an adaptive strategy enables different heterothermic species to substantially suppress their energy needs during periods of severely reduced food availability, (ii) the torpor phenotype implies marked metabolic adaptations from the whole organism down to cellular and molecular levels, and (iii) the torpid state is associated with highly efficient rehabilitation and protective mechanisms ensuring the continuity of proper bodily functions. Comparison of mechanisms in monotremes and marsupials is warranted for understanding the origin and evolution of mammalian torpor.

## Linked entities

- **Chemicals:** hydrogen sulfide (PubChem CID 402), H2S (PubChem CID 402)

## Full-text entities

- **Genes:** Fcgr3 (Fc receptor, IgG, low affinity III) [NCBI Gene 14131] {aka CD16}, Gsk3b (glycogen synthase kinase 3 beta) [NCBI Gene 84027], GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, Nfe2l2 (nuclear factor, erythroid derived 2, like 2) [NCBI Gene 18024] {aka Nrf2}, Mpst (mercaptopyruvate sulfurtransferase) [NCBI Gene 246221] {aka 3MST, Mst}, Mcl1 (myeloid cell leukemia sequence 1) [NCBI Gene 17210] {aka Gm52627, Mcl-1}, Tmbim6 (transmembrane BAX inhibitor motif containing 6) [NCBI Gene 110213] {aka 5031406P05Rik, Bi1, Tegt}, Ppargc1a (peroxisome proliferative activated receptor, gamma, coactivator 1 alpha) [NCBI Gene 19017] {aka A830037N07Rik, Gm11133, PGC-1, PPARGC-1-alpha, Pgc-1alpha, Pgc1}, Bcl2l1 (BCL2-like 1) [NCBI Gene 12048] {aka Bcl(X)L, Bcl-XL, Bcl2l, BclX, bcl-x, bcl2-L-1}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, TXNIP (thioredoxin interacting protein) [NCBI Gene 10628] {aka ARRDC6, EST01027, HHCPA78, THIF, VDUP1}, Cd68 (CD68 antigen) [NCBI Gene 12514] {aka Lamp4, Scard1, gp110}, Insr (insulin receptor) [NCBI Gene 16337] {aka 4932439J01Rik, CD220, D630014A15Rik, IR, IR-A, IR-B}, IL-1beta [NCBI Gene 101839008], Stat6 (signal transducer and activator of transcription 6) [NCBI Gene 20852], Foxo3 (forkhead box O3) [NCBI Gene 56484] {aka 1110048B16Rik, 2010203A17Rik, FKHRL1, Fkhr2, Foxo3a}, Stat1 (signal transducer and activator of transcription 1) [NCBI Gene 20846] {aka 2010005J02Rik}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, Ghrl (ghrelin) [NCBI Gene 58991] {aka 2210006E23Rik, Ghr, MTLRP, MTLRPAP, m46}, catalase [NCBI Gene 101824222], Stat3 (signal transducer and activator of transcription 3) [NCBI Gene 20848] {aka 1110034C02Rik, Aprf}, Thioredoxin [NCBI Gene 101840972], Cth (cystathionine gamma lyase) [NCBI Gene 107869] {aka 0610010I13Rik, CGL, CSE, Cys3}, Fcgr2b (Fc receptor, IgG, low affinity IIb) [NCBI Gene 14130] {aka CD32, F630109E10Rik, Fc[g]RII, FcgRII, Fcgr2, Fcgr2a}, GSK3beta [NCBI Gene 101836282], ACE [NCBI Gene 101824864], FSD1 (fibronectin type III and SPRY domain containing 1) [NCBI Gene 79187] {aka GLFND, MIR1}, IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, Hmox1 (heme oxygenase 1) [NCBI Gene 15368] {aka D8Wsu38e, HO-1, HO1, Hemox, Hmox, Hsp32}, Insulin [NCBI Gene 101823595], Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, Gsk3b (glycogen synthase kinase 3 beta) [NCBI Gene 56637] {aka 7330414F15Rik, 8430431H08Rik, GSK-3, GSK-3beta, GSK3}, Lep (leptin) [NCBI Gene 16846] {aka ob, obese}, ribosomal protein S6 [NCBI Gene 101966465], Adiponectin [NCBI Gene 101823810], GIP [NCBI Gene 101827768], Txn1 (thioredoxin 1) [NCBI Gene 22166] {aka ADF, Trx1, Txn}, Stat5a (signal transducer and activator of transcription 5A) [NCBI Gene 20850] {aka STAT5}, Keap1 (kelch-like ECH-associated protein 1) [NCBI Gene 50868] {aka INRF2, mKIAA0132}, Rhd (Rh blood group, D antigen) [NCBI Gene 19746] {aka Rh, Rhced, Rhl1}, Leptin [NCBI Gene 101837349], Ager (advanced glycosylation end product-specific receptor) [NCBI Gene 81722] {aka RAGE}, Cbs (cystathionine beta-synthase) [NCBI Gene 12411] {aka HIP4}, interferon gamma [NCBI Gene 101825431], CSE [NCBI Gene 1433], Sirt1 (sirtuin 1) [NCBI Gene 93759] {aka SIR2L1, Sir2, Sir2a, Sir2alpha}, Bcl2 (B cell leukemia/lymphoma 2) [NCBI Gene 12043] {aka Bcl-2, C430015F12Rik, D630044D05Rik, D830018M01Rik}, TXNIP [NCBI Gene 101842562], Txnip (thioredoxin interacting protein) [NCBI Gene 56338] {aka 1200008J08Rik, Hyplip1, THIF, Tbp-2, VDUP1}, IL-10 [NCBI Gene 101840942], CBS [NCBI Gene 101827489]
- **Diseases:** MR (MESH:D008659), mitochondrial dysfunction (MESH:D028361), uremia (MESH:D014511), immunological depression (MESH:D007154), hypoxic (MESH:D002534), I. (MESH:D006969), mass loss (MESH:C536030), atrophy of the intestinal mucosa (MESH:D007410), Inflammation (MESH:D007249), adiposity (MESH:D018205), neuronal apoptosis (MESH:D065703), sarcopenia (MESH:D055948), muscle atrophy (MESH:D009133), reperfusion damage (MESH:D015427), brain injury (MESH:D001930), ischemia (MESH:D007511), depression (MESH:D003866), mucosal atrophy (MESH:D001284), brain damage (MESH:D001925), glucose intolerance (MESH:D018149), tauopathies (MESH:D024801), hypothermia (MESH:D007035), cardiovascular impairments (MESH:D002318), death (MESH:D003643), neuroinflammation (MESH:D000090862), obesity (MESH:D009765), immunodeficiency (MESH:D007153), CKD (MESH:D051436), fat accumulation (MESH:D004620), lung remodeling (MESH:D008171), neuro-degenerative diseases (MESH:D019636), anoxia (MESH:D000860)
- **Species:** Lemur (genus) [taxon 9446], Microcebus murinus (gray mouse lemur, species) [taxon 30608], Eliomys quercinus (garden dormouse, species) [taxon 53277], Homo sapiens (human, species) [taxon 9606], Ursus arctos (brown bear, species) [taxon 9644], Lemuridae (lemurs, family) [taxon 9445], Chiroptera (bats, order) [taxon 9397], Myotis lucifugus (little brown bat, species) [taxon 59463], Rattus norvegicus (brown rat, species) [taxon 10116], Callospermophilus lateralis (golden-mantled ground squirrel, species) [taxon 76772], Cricetus cricetus (black-bellied hamster, species) [taxon 10034], Ictidomys tridecemlineatus (thirteen-lined ground squirrel, species) [taxon 43179], Sminthopsis macroura (Australian stripe-faced dunnart, species) [taxon 9302], Marmota monax (groundhog, species) [taxon 9995], Mesocricetus auratus (golden hamster, species) [taxon 10036], Glis glis (Fat dormouse, species) [taxon 41261], Phodopus sungorus (Djungarian hamster, species) [taxon 10044], undetermined Sciuridae 'chipmunks' (chipmunks, species) [taxon 54071], Widjajachloa producta (species) [taxon 323911], Escherichia coli (E. coli, species) [taxon 562], Spermophilus citellus (European ground squirrel, species) [taxon 9997], Marmota flaviventris (yellow-bellied marmot, species) [taxon 93162], Nothofagus pumilio (species) [taxon 28950], Glis (fat dormice, genus) [taxon 41260], Echinops telfairi (lesser hedgehog tenrec, species) [taxon 9371], Cricetinae (hamsters, subfamily) [taxon 10026], Dromiciops gliroides (monito del monte, species) [taxon 33562], Drosophila melanogaster (fruit fly, species) [taxon 7227], Elephantulus (long-eared elephant shrews, genus) [taxon 28736], Metatheria (marsupials, clade) [taxon 9263], Trochilidae (hummingbirds, family) [taxon 9242], Marmota marmota (European marmot, species) [taxon 9993], Ursus americanus (American black bear, species) [taxon 9643], Rhinolophus ferrumequinum (greater horseshoe bat, species) [taxon 59479], Sciuromorpha (squirrels, suborder) [taxon 33553], Urocitellus parryii (Arctic ground squirrel, species) [taxon 9999], Erinaceus europaeus (common hedgehog, species) [taxon 9365], Tamias striatus (eastern chipmunk, species) [taxon 45474], Mus musculus (house mouse, species) [taxon 10090], Rhinolophus (genus) [taxon 49442]
- **Mutations:** methionine to cysteine

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC7854925/full.md

## References

254 references — full list in the complete paper: https://tomesphere.com/paper/PMC7854925/full.md

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Source: https://tomesphere.com/paper/PMC7854925