Skip to main content
. Author manuscript; available in PMC: 2015 Jun 3.
Published in final edited form as: Mini Rev Med Chem. 2006 Aug;6(8):875–884. doi: 10.2174/138955706777934964

Table 2.

Evidence for Tissue/Blood Borne Molecules in Torpid Animals that Induce a Protective Mechanism

Source Species Source Tissue Pharmacologic Effect Target Species Target Tissue Administered Reference
TLS brown fat decreases primary immune response hamster spleen fragments cell culture [139]
AL brain extract decreases metabolism and Tb*to4°C rat systemic iv [23,24]
TLS brain extract decrease metabolism rat systemic iv [26]
AL brain extract decreases metabolism and Tb mouse systemic iv [25]
TLS brain extract decreases cell division Chinese hamster ovary cells (CHO) cell culture [87]
JGS, AGS brain and small intestine epitheluim decreases brain temperature and awake state; increases slow wave sleep mouse brain ip [2729]
JGS plasma decreases metabolism mouse systemic ip [31]
JGS urine decreases Tb mouse systemic ip [31]
TLS plasma increases intercellular adhesion molecule-1 (ICAM-1) expression and monocyte adhesion rat cerebral microvascular endothelial cells cell culture [141]
BB serum increases protection from ischemia-reperfusion rabbit heart perfuse [12]
TLS, WC plasma decreases cell proliferation suggesting mechanism of immunosuppression mouse spleenocytes cell culture [140]
*

Tb = body temperature; AL = African lungfish